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"Once someone has had
the good fortune to share a true love affair with a
Golden Retriever, one's
life and one's outlook is never quite the
same."
~ Betty White ~
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TELOMERASE CANCER VACCINE STUDY FOR DOGS AND CATS WITH EXTERNAL NON-RESECTABLE CANCERS

The Department of Oncology at the Veterinary Specialty Center of the Hudson Valley is looking for canine and feline patients with external non-resectable cancers to participate in a clinical trial with our Telomerase Cancer Vaccine.
An external, superficial tumor would be biopsied here at VSCHV pre vaccine immunotherapy and also at the completion of the vaccine series (5 treatments-- 2 weeks apart) also administered here.
We are evaluating the T cell infiltration into the tumor and telomerase antibody response. Patient will receive vaccine at N/C but additional fees for administration apply and will be discussed and clearly presented to any interested client.
For more information, please call 845-632-3200.
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Golden Retriever Lifetime Study
Morris Animal Foundation's Golden Retriever Lifetime Study is a groundbreaking effort to learn how to prevent cancer and other diseases. It is the largest and longest observational study ever undertaken to improve the health of dogs. The study will enroll up to 3,000 Golden Retrievers and will last 10 to 14 years.
A Golden Opportunity to Improve the Health of Golden Retrievers
Why Should Your Dog Participate?
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Cancer is the #1
cause of death in dogs over the age
of 2, and more than half of all
Golden Retrievers die of the
disease.
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It will identify the
genetic, nutritional and
environmental risk factors for
cancer and other diseases affecting
Golden Retrievers.
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This study is
expected to provide valuable
information into prevention
strategies, early diagnosis and new
treatments for cancer and other
canine diseases.
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The Golden Retriever
Lifetime Study will help to improve
the health of future generations of
Golden Retrievers and will help
create a healthier tomorrow for all
dogs.
Who Can Participate?
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Highly committed
Golden Retriever owners living in
the continental United States.
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Owners who are over
the age of 18.
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Dogs that are
healthy and under 2 years of age at
the time of enrollment.
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Dogs that have a
three-generation pedigree.
What Is Expected of You?
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Agree to participate
for the life of your dog
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Select a
veterinarian who agrees to
participate with you
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Complete online
questionnaires regarding your dog's
food type and feeding habits,
environmental exposures,
behavior/temperament, disease
events, etc.
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Visit your dog's
veterinarian for annual exams and
sample collection (blood, urine,
feces, hair, and toenail clippings)
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When applicable,
allow collection of tumor samples
for evaluation
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Be willing to
consider a necropsy (post mortem
examination) when your dog's life
ends
Note: You are
responsible for all costs associated
with the annual exam, sample
collection and laboratory test
results. Morris Animal Foundation
will reimburse you for up to $75 of
these costs per year after
verification that the exam and
sample collection has been
completed.
If you choose, you may also donate
this compensation directly back to
Morris Animal Foundation to support
the Golden Retriever Lifetime Study.
To determine if your dog is eligible
for participation in the Golden
Retriever Lifetime Study, you must
first register for the Canine
Lifetime Health Project. After you
sign up for the Canine Lifetime
Health Project, you will be notified
by email if your dog qualifies for
the Golden Retriever Lifetime Study
or any studies managed through this
project.
Special Update from the GRF and the Morris Animal
Foundation
The Golden Retriever Foundation and GRCA are excited
to announce that the Golden Retriever Lifetime Study
is underway! This is an unprecedented longitudinal
study of factors that may influence the development
of cancer and other diseases in Goldens. It is the
innovation of the Morris Animal
Foundation, and will succeed only with full support
from the Golden community.
If you own a Golden of known pedigree who is 2 years
or younger, and you are willing to commit to
participation with your dog for its entire lifespan,
you are encouraged to register for this important
study. Please take a few minutes to check out the
details at:
(https://www.caninelifetimehealth.org/#About/GoldenRetrieverLifetimeStudy)
At last notice, there were already over 200 eligible
Goldens already registered for the Canine Lifetime
Health Project, out of which the participants for
the GRLS will be selected. Once you register, watch
your email for more information and the next steps.
50 Goldens will be used in the initial beta phase of
the project, which launched just last week. All
other Goldens who are eligible, and registered with
CLHP, will be invited to enroll in a few weeks. Be
patient while the "kinks" are worked out of the
system. Morris Animal Foundation is committed to
their goal of 3000 Goldens participating in the
study.
An important aspect of the study is that a wide
range of pedigrees and geographical regions is
needed. Spread the word to your friends with
Goldens, especially those who may not be members of
GRCA or acquainted with the GRF, and encourage them
to register. Field dogs, conformation dogs, agility
dogs, obedience and rally dogs, pet dogs -- we all
need to play to win this game!
To recap:
1. Register for the Canine Lifetime Health Project
at the website noted above.
2. Wait to hear from Morris Animal Foundation that
your dog is invited to enroll in GRLS.
3. Commit to the project and help our breed live
longer, healthier lives in the future.
Look for an article on page 32 of the March/April
2012 GRNews on GRLS -- and register today!
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Mason Golden Retriever Study -- Goldens needed who are 6 to 8 years of age!
http://www.vet.upenn.edu
The Mason lab at the University of Pennsylvania
School of Veterinary Medicine is investigating the
possibility that a gammaherpesvirus can infect dogs
and may contribute to lymphoma. The virus is thought
to be highly similar to Epstein-Barr Virus that
infects the majority of humans.
In most humans, infection is asymptomatic (no
clinical signs), but in a very small subset of
people, the virus is associated with lymphomas.
Mason’s lab has shown that some dogs (like people)
can be infected with an EBV-like virus and that this
appears to be associated with lymphoma in some cases
(Evidence of an oncogenic gammaherpesvirus in
domestic dogs. Huang et al. Virology. 2012 Mar 7).
Using a relatively simple blood test, Mason’s lab
can determine whether dogs have been exposed to an
EBV-like virus. They now aim to screen approximately
500 healthy Golden Retriever dogs between 6 and 8
years of age to determine whether they are infected
with the virus.
Participating dogs will be evaluated every 6 months
for 2 years to determine whether the presence of
increasing amounts of virus and antibodies to the
virus predicts which dogs many go on to develop
lymphoma.
The study aims to provide very important information
about a possible environmental cause of cancer and
may lead to future anti-viral therapies for cancer.
This study is supported by the National Institutes
of Health.
We invite All Owners of Golden Retrievers to
Take Part in This Study
All owners of healthy Golden
Retrievers are invited to participate in an
unprecedented study to investigate the possibility
that a particular virus (a gammaherpesvirus) can
infect Golden Retriever dogs and that this infection
contributes to the development of lymphoma in some
dogs.
Eligibility
If you have a healthy Golden
Retriever dog that has not been previously diagnosed
with cancer, and is between 6 and 8 years of age you
may be eligible to participate in this study.
Complete information regarding the study and study
eligibility can be found on the consent form
(download below).
Samples Required for the Study
The study involves taking a blood
sample from your dog once every six months for two
years.
If your dog develops lymphoma while on the study, a
biopsy of the malignant lymph node tissue will be
taken and used to confirm the diagnosis and
determine whether this virus is involved in the
tumor.
Blood samples and lymph node biopsies can be taken
at your local veterinarian and sent to the
University of Pennsylvania School of Veterinary
Medicine.
About Costs: Please note that we do not have funds
to cover any costs associated with visits to your
veterinarian or costs associated with lymph node
biopsies or blood samples. Funds are available to
pay for shipping of samples to UPenn from your local
veterinarian and for all laboratory tests that look
for the virus in the blood and in any tumor tissue.
Study Participant Information for Golden
Retriever Dogs
If you would like to participate in
the study, please download:
Take these to your veterinarian.
Please complete the consent form and ask your
veterinarian to complete the examination form.
Both forms should be submitted to UPenn with your
samples.
All samples should be sent overnight to the
following address:
Attention: Dr. Nicola Mason
Room 335, Hill Pavilion
University of Pennsylvania School of Veterinary
Medicine
380 South University Avenue
Philadelphia, PA 19107
Contact Information
Golden Retriever owners may also contact Rhonda
Hovan (GRCA Health Committee member) by telephone at
330-668-0044 or 330-338-4236 (cell) or by e-mail at
RhondaHovan@aol.com.
Related Resources
If you would like to contribute to canine cancer
research in the Mason laboratory, please send your
check made payable to the Trustees of the University
of Pennsylvania and note that it should be
designated to the Mason Cancer Research Fund. Please
mail to:
Office of Development
School of Veterinary Medicine
3800 Spruce Street, Suite 172E
Philadelphia, PA 19104
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McMaster University Researchers in Hamilton, Ontario, Discover Drug that Kills Cancer Stem Cells!
The Spectator Newspaper, Hamilton, Ontario, Canada
Reporter: Joanna Frketich
McMaster researchers have discovered a drug commonly
used for Parkinson's Disease and schizophrenia kills
cancer stem cells without the toxic side-effects of
other treatments.
Patients taking thioridazine for Parkinson's and
schizophrenia have 10 times less instance of cancer
after being on the drug for a few years.
"We're connecting dots that we weren't connecting
before," said Dr. Mick Bhatia, principal
investigator of the study and scientific director of
McMaster's Stem Cell and Cancer Research Institute.
"We're excited we have something interesting, but
we're always nervous because we want to make sure it
helps people. The impact of this will be determined
if we can put some patients in remission and
certainly that's my romantic goal."
He expects a small number of Hamilton leukemia
patients with no other treatment options will have
access to the drug through a clinical trial within a
year. He's also hoping to set up a second trial at
another Ontario cancer centre.
"It's not everyday you find a drug you can move into
the clinic," said Bhatia. "The only thing we can
hope for is that what we've seen in the laboratory,
we're hoping will work in a patient."
If it works, it could dramatically change cancer
treatment. Thioridazine on its own reduced leukemia
stem cells by 50 per cent in 24 hours in mice
injected with primary human samples, found the study
published in the science journal CELL.
"That was quite surprising," said Bhatia. "We have
certainly not seen any drug we've tested have that
kind of potency."
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Improving Ability to Predict
Cancer Spread
Morris Animal Foundation–Funded
Clinical Trial
D09CA-031, North Carolina State University, Dr.
Marlene L. Hauck
Samples Requested: Canine soft-tissue sarcomas
(including fibrosarcomas, hemangiopericytomas,
peripheral nerve sheath tumors, liposarcomas,
leiomyosarcomas, rhabdomyosarcomas and
undifferentiated sarcomas)
Study Outline: Soft-tissue sarcomas are the most
common type of solid tumors in dogs. They are
locally invasive tumors with a high local recurrence
rate. The metastasis rate varies from 5 to 40
percent depending on the tumor type and grade. The
laboratory of Dr. Marlene Hauck is evaluating the
genetic changes that are seen in soft-tissue
sarcomas that metastasize versus those that do not.
The goal is to identify a gene or protein expression
"signature" that will more accurately predict which
dogs will go on to develop metastasis in order to
improve the outcome for dogs with soft-tissue
sarcomas.
Sample Submission: Researchers are interested in
receiving biopsy samples of dogs with soft-tissue
sarcoma. It is recommended that the referring or
primary veterinarian submit the sample. Researchers
welcome any questions referring veterinarians or
owners may have.
Sample Collection and Shipping: For each sample
submission, the following is required:
Representative non-necrotic pieces of the tumor
(preferably at least 1 cm3 or equivalent) collected
as aseptically as possible in each of the following:
1. RNA stabilization solution (which researchers
will provide)
It is very important that samples are placed in this
solution immediately after biopsy.
2. Formalin
Basic patient information, clinical history and
associated pathology reports relating to this tumor
Please contact the Hauck Lab at North Carolina State
College of Veterinary Medicine in advance of sample
collection, so that we may provide detailed
collection instructions and arrange shipment of RNA
stabilization solution and tumor samples.
Contact Details for Dr. Marlene Hauck's Lab:
Julie Fisher, Research Specialist
Room 326, CVM Research Building
Department of Clinical Sciences
College of Veterinary Medicine
North Carolina State University
4700 Hillsborough Street
Raleigh, NC 27606
Phone: 919.513.8276 Fax: 919.513.7301
E-mail:
julie_fisher@ncsu.edu
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SEARCHABLE CLINICAL TRIALS
DATABASE FOR CANCER IN PET ANIMALS
https://cvmsecure.missouri.edu/vcs/ClinicalTrials/publicAccess/
Welcome to the Veterinary Cancer Trials website.
This site is sponsored by the Veterinary Cooperative
Oncology Group (VCOG), a group of board-certified
veterinary oncologists and associated specialists
assembled to promote high quality veterinary
oncology collaborative investigations through the
establishment of common goals and endpoints for the
purpose of benefitting both animals and people
affected by cancer. VCOG represents the collective
knowledge of the specialty of veterinary oncology.
This site was designed for use by everyone who
participates in the treatment of pet animals with
cancer, including pet owners, general practice
veterinarians, and oncologists and other specialty
veterinarians. Information is provided to inform
both private practice and academic veterinarians,
and to promote accrual for the timely completion of
clinical trials while providing state-of-the-art
treatment options for pets with cancer.
To use this site, you may simply click the box for
searching for trials based on specific criteria
(type of cancer, geographic location of clinical
trial, or species of animal), or you can browse all
trials. Each trial description provides basic
information needed to determine whether a pet is
eligible for a trial, what a trial entails, and an
appropriate contact person if there is a trial of
interest. Information is updated at least monthly.
If you are a designated contact for an institution
that initiates clinical trials, you can log in as
instructed. This will allow you to enter, edit, or
remove only trials from your institution. If you are
a member of the Veterinary Cancer Society, you will
be able to log in using your VCS website login
information. This will allow you to view information
that is not displayed for the general public such as
details of trial design. You will not be able to
modify any trial data for any institution.
Thank you for visiting this site. Our goal is to
promote cutting edge therapy of pets with cancer and
facilitate timely completion of clinical trials so
that promising new therapies can enter clinical
practice sooner.
For questions related to this site, please contact
vct@vetcancertrials.org
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Researchers at the University of
Guelph have started their large Hemangiosarcoma
Validation Study, measuring a marker for
Hemangiosarcoma. This is such exciting news, and 52
Golden Retrievers from the Greater Toronto Area, are
participating in this study. All the dogs enrolled
in the study are 7 years of age or older. Males and
females, intact and neutered/spayed, are involved in
this study. Each dog is receiving a CBC, a
biochemical profile, urinalysis, and an abdominal
ultrasound, performed by a board certified internal
medicine specialist. All testing is taking place at
the Mississauga-Oakville Veterinary Emergency
Hospital. There is no charge for the testing, and a
full report of the blood work and ultrasound
findings are being sent to each of the participants'
regular veterinarians.
For further information, please contact:
Gordon M. Kirby DVM, MSc, PhD
Associate Dean, Research & Innovation
Professor, Department of Biomedical Sciences
Ontario Veterinary College
University of Guelph
Guelph, Ontario, Canada
N1G 2W1
Telephone: 519-824-4120; Extension 54948 or 54796
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Chinese herbal
drug tested
Vet Med offers clinical trial for dogs with cancer
Tuesday, Sep. 28, 2010

PULLMAN - WSU's College of
Veterinary Medicine is offering a financial
incentive to pet owners whose dogs participate in a
clinical trial regarding B cell lymphoma, a type of
blood cell cancer.
Artemisinin is a drug derived from the plant
Artemisia annua. It has been traditionally used by
Chinese herbalists in the treatment of skin diseases
and malaria. In addition to its well-known
antimalarial properties, the drug has recently
aroused interest as an anticancer drug.
In the laboratory, the drug causes cancer cell death
and changes that could sensitize cancers making them
more susceptible to common chemotherapy drugs. WSU’s
clinical trial will examine this effect in dogs with
cancer.
In order to determine the efficacy of compounds used
to treat cancer in humans or animals, physicians and
veterinarians who specialize in cancer often conduct
clinical trials. Trials offer people or animal
owners in this case some form of compensation for
volunteering their dog that has cancer.
For this study, WSU is limiting care expenses an
owner pays to $300, if their dog meets a special set
of criteria for enrollment.
The study is funded by the Washington State Life
Sciences Discovery Fund. Costs associated with the
collection of samples, re-evaluating disease burden,
bloodwork for chemotherapy, chemotherapy drug, and
administration are covered, when performed at the
WSU Veterinary Teaching Hospital.
Lymphoma is the most common form of blood cell
cancer in dogs and one of the most common forms
overall. It strikes any age and breed of dog,
although certain breeds are more susceptible. For
dogs with B cell multicentric lymphoma, most will
die on average within a year of diagnosis with
aggressive treatment.
Standard chemotherapy for B cell lymphoma is well
tolerated and provides an excellent quality of life
during treatment. Now WSU veterinary cancer
specialists want to further improve the
well-established chemotherapy’s impact.
For more complete details and to learn more about
this clinical trial see:
http://vetmed.wsu.edu/researchVCS/Artemisinin.aspx
or contact Pam Thompson at
509-335-0711 or
pat@vetmed.wsu.edu.
By Charlie Powell, College of Veterinary Medicine
Telephone: 519-824-4120; Extension 54948 or 54796
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K9 Hemangiosarcoma Clinical Trial
The Department of Oncology at VSCHV and the
Department of Radiation Oncology at the AMC are
collaborating for a clinical study to evaluate a new
protocol for K9 Hemangiosarcoma (HSA). As we
all know, this disease is a challenge to treat with
limited long term survival despite chemotherapeutic
intervention. Newer theories are based on
immunotherapy and exploiting angiogenesis
inhibition.
This study seeks to compare the use of 2Gy
Total Body Irradiation (TBI), a non-lethal dose,
which does not require supportive care, in order to
decrease T regulatory cells thereby promoting an
improved immune response with either an autogenous
vaccine (from same patient) or an allogeneic vaccine
(from another HSA). 2 abstracts support the
use of TBI as an adjunct to immunotherapy:
1) Blood volume 102 (part 1) Issue 11, Start page
76a (abstract # 256) ; November 16, 2003
Breaking tolerance in stable mixed chimeric dogs
with low-dose TBI and donor or recipient lymphocyte
infusion
*Taranova,A.G.; Georges,G.E.; Yunusov,M.; Storb,R.F.;
Nash,R.A . Fred Hutchinson Cancer Research Center ;
University of Washington
2) Cell Mol Immunol . 2010 Mar;7(2):157-62. Epub
2010 Feb 8. Enhancement of antitumor immunity by
low-dose total body irradiation is associated with
selectively decreasing the proportion and number of
T regulatory cells.
*Liu R, Xiong S , Zhang L , Chu Y . Department
of Immunology, Shanghai Medical College,Institute
for Immunobiology, Key Laboratory of Molecular
Medicine of Ministryof Education, Fudan University,
Shanghai.
Abstract:
Low-dose total body irradiation (LTBI) is used in
the treatment of some cancers mainly for immune
enhancement rather than cell killing. However, the
mechanism underlying LTBI remains unknown. In this
study, by analyzing the immune patterns of
lymphocytes, we found that the percentage and
absolute number of CD4(+)CD25(+)Foxp3(+) regulatory
T cells are markedly decreased in naive mice
following treatment with LTBI. On the contrary, the
CD4(+)CD44(+)/CD8(+)CD44(+) effect or-memory T cells
are greatly increased. Importantly, naive mice
treated with dendritic cell-gp 100 tumor vaccines
under LTBI induced an enhancement of
antigen-specific proliferation and cytotoxicity as
well as interferon-gamma (IFN-gamma) secretion
against F10 melanoma tumor challenge, compared to
treatment with either the tumor vaccine or LTBI
alone. Consequently, the treatment resulted in a
reduced tumor burden and prolonged mouse survival.
Our data demonstrate that LTBI's enhancement of
antitumor immunity was mainly associated with
selectively decreasing the proportion and number of
T regulatory cells,implying the potential
application of the combination of LTBI and a tumor
vaccine in antitumor therapy.
WHAT YOU CAN DO:
You can refer your patient to VSCHV for surgical
resection where applicable and creation of
autogenous vax. Please do not hesitate to call
if you have a case to discuss.
OR
Your veterinarian can sample the tissue as long as
it is harvested with sterile technique, placed in
sterile saline and saved in a standard refrigerator.
0.5cm of tumor is needed. A biopsy report will
also be required. Again, please do not
hesitate to call if you have any questions.
Following tissue confirmation and staging, each of
these patients will receive:
2Gy Total Body Irradiation at AMC followed with
autogenous vax
What if I have a biopsy that supports HSA but do not
have a sample for the vax?
Patients with a biopsy report but no tissue for
vaccine will be eligible for allogeneic vax after
2Gy TBI. We are looking to recruit patients to
enroll in this study, and ask for your assistance.
Eligible candidates are dogs at least 1 year of age.
There must be a diagnosis of Hemangiosarcoma via
histopathology (spleen, liver, subcutaneous or
other). Cutaneous HSA will not be included in
this study. There is no cost for vaccines.
Costs to be incurred by the client will include
tissue harvesting, labwork, radiology, total body
irradiation, medical shipping and exams. A medical
plan is provided to the owners at the initial
consult to clearly define fees.
We hope that this invitation to participate in an
exciting new clinical study will provide a benefit
to your practice and patients. We look forward
to hearing from you regarding potential candidates.
Please use the referral form on our website at
www.vschv.com or
if you have any questions, please contact:
Joseph A. Impellizeri, DVM, DACVIM (O) in the
Department of Oncology at VSCHV at (845) 632-3200 or
info@vschv.com
John Farrelly, DVM, MS, DACVIM (O), DACVR (RO),
Director of Radiation Oncology at AMC at (212)
329-8794
The Veterinary Specialty Center of the Hudson Valley
(VSCHV) is located at:
1285 RT 9
Wappingers Falls, NY. 12590
www.vschv.com
24/7/365 days a year
The Animal Medical Center (AMC) is located at:
510 East 62nd Street
New York, NY 10065
www.amcnyc.org
To refer a patient or for directions, please visit
us on our website at
www.vschv.com or call 1.845.632.3200
This message was sent from Veterinary Specialty
Center of the Hudson Valley to
cminnier@epix.net.
It was sent from: Veterinary Specialty Center of the
Hudson Valley, 1285 Rt 9, Wappingers Falls, NY
12590.
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Canine patients with
B cell lymphoma
Patient Disease
Canine patients with B cell lymphoma
Study Name
Development of Artemisinin Compounds for Cancer
Treatment.
Purpose of the Study
Lymphoma is the most common form of hematopoietic
cancer in dogs and one of the most common forms
overall. It can strike any age and breed of dog,
although certain breeds have a greater frequency of
the disease. Multicentric lymphoma is characterized
by non-painful enlargement of lymph nodes. Despite
improvements in chemotherapy, most dogs will die
from this disease, with an average survival of
approximately one year after diagnosis. Standard
chemotherapy for B cell, multicentric lymphoma is
doxorubicin-based treatment. The majority of dogs
tolerate chemotherapy well with good to excellent
quality of life during treatment.
Artemisinin is a drug derived from the plant
Artemisia annua, traditionally used by Chinese
herbalists in the treatment of illnesses such as
skin diseases and malaria. Besides its well-known
anti-malarial properties, the drug has recently
aroused interest as an anti-cancer drug. In vitro
studies show that the drug causes cancer cell death
and molecular changes that could sensitize cancers
to common chemotherapy drugs.
This clinical trial will evaluate the ability of
artemisinin to sensitize B-cell lymphoma to
doxorubicin chemotherapy in dogs, compared to a
placebo.
This will be done by evaluating extent of disease
thoroughly (staging), including a biopsy of a lymph
node. The dog will then receive artemisinin or a
placebo for three days prior to a second biopsy
being collected. After this, dogs will receive
either artemisinin or placebo and standard
doxorubicin chemotherapy every three weeks for three
cycles. Following chemotherapy, dogs will continue
the assigned capsules and be monitored carefully for
duration of response. Dogs must receive the biopsies
and chemotherapy treatments at the WSU-VTH.
Artemisinin or placebo will be assigned randomly,
and neither owner nor clinician will know which the
dog is receiving.
Patient Entry Criteria
Certain criteria will determine if your dog
qualifies for this study. Dogs with B cell,
multicentric lymphoma may be eligible for this
study. They may not have received previous treatment
for their lymphoma, including prednisone. Dogs with
spread of the lymphoma beyond the lymph nodes to
other locations in the body (liver and spleen) who
are asymptomatic may be eligible (Stage III and IV
dogs). Patients must be otherwise in good health and
have no cardiac, renal, or hepatic insufficiency.
Owners must consent to a postmortem examination
(autopsy) at the time their dog dies or is
euthanized if still on protocol.
Owner Responsibilities
The owner is financially responsible for costs
associated with the diagnosis and staging of the
disease (such as blood tests, chest X-rays, flow
cytometry, abdominal ultrasound, bone marrow
cytology, etc.) to determine the dog’s eligibility
for enrollment in this study. If a dog is accepted
into the study, these costs will be limited to $300.
The owner is expected to make and keep all
appointments according to the study protocol, which
will include initial examination and biopsies over a
four-day period, and three chemotherapy treatments
on an every three week schedule. Rechecks will be
performed monthly thereafter. The owner will also be
expected to keep a drug log to record
administration. Doxorubicin as a single-agent
therapy will be administered as part of this
protocol. This is a standard and effective treatment
that is likely to result in a complete remission for
most dogs.
Financial Incentives
This study is funded by the Washington State Life
Sciences Discovery Fund for specific care in the
study. Costs associated with the collection of
samples, re-evaluating disease burden, bloodwork for
chemotherapy, chemotherapy drug, and administration
are covered, when performed at the WSU-VTH.
Laboratory costs outside of the VTH are not covered
by the study.
Contact Information
Please contact Pam Thompson at 509-335-0711 or
pat@vetmed.wsu.edu if you are interested
in learning more about this clinical trial.
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Dogs with
Osteosarcoma (bone cancer)
Patient Disease
Canine patients with osteosarcoma
Study Name
Effects of Anti-Angiogenic Chemotherapy on
Circulating Endothelial Cells in Dogs with
Osteosarcoma
Purpose of the Study
Chemotherapy typically is administered at
maximally tolerated (high) doses at regular
intervals, such as once every 3 weeks. Although the
chemotherapy drug kills rapidly growing cancer
cells, some normal cells (such as those in the bone
marrow and intestines) also are affected and a
recovery period is needed for these tissues to renew
themselves. Unfortunately, this gap in treatment can
allow the cancer cells time to grow as well. Anti-angiogenic
chemotherapy or low-dose chemotherapy is defined as
the frequent administration of low doses of
chemotherapy with no prolonged breaks in treatment.
One of the main effects of anti-angiogenic
chemotherapy is to decrease the growth of new blood
vessels that supply the tumor (known as
“angiogenesis”), thereby decreasing the growth and
spread of the cancer cells. This type of
chemotherapy has been demonstrated to reduce the
number of circulating endothelial cells in people
with different types of cancer and therefore
circulating endothelial cells may be a potential
biomarker linked to the success of anti-cancer
therapies. One of the chemotherapy drugs being used
currently at Washington State University in canine
anti-angiogenic chemotherapy protocols is lomustine,
which has the advantage of being administered by
mouth at home. The goal of this study is to
determine whether anti-angiogenic lomustine
decreases the number of circulating endothelial
cells and tumor angiogenesis in dogs with
osteosarcoma.
Patient Entry Criteria
Certain criteria determine patient eligibility.
Patients must be in good health prior to starting
this study. Owners are responsible for the cost of
blood work, urinalysis, chest X-rays and any other
tests recommended by your pet’s oncologist prior to
entry into the trial. Dogs with cytologically or
histopathologically confirmed osteosarcoma may be
eligible for this study. Patients must not have
received surgery, chemotherapy or radiation therapy
for at least 2 weeks prior to study entry. Dogs with
catheters for blood collection will be excluded from
this study.
Owner Responsibilities
Owners are responsible for the initial diagnostic
testing, including physical examination, blood work,
urinalysis, chest X-rays and any other tests
recommended by your pet’s oncologist. Additionally,
the cost of the lomustine is the responsibility of
the owner. The owner is expected to make and keep
all appointments according to the study protocol,
which will include initial examination and staging
tests, and recheck appointments prior to initiation
of low-dose lomustine, and again four weeks later.
The study is completed after this four week recheck.
Financial Incentives
The study will pay for a complete blood count and
chemistry panel prior to starting low-dose lomustine,
as well as for the recheck evaluation, complete
blood count and chemistry panel on week 4 of the
study. All other costs relating to your pet’s care
including the cost of diagnosing and staging prior
to entering the study (approximately $500-$800),
will be the responsibility of the owner. Any
complications associated with treatment will also be
the responsibility of the owner.
Contact Information / Prinicipal
Investigator
Please contact Dr. Christie Anderson at (509)
335-0711 or via email at
canderson@vetmed.wsu.edu if you are interested
in learning more about this clinical trial.
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AKC Canine Health
Foundation News Alert
Samples Needed for Canine Melanoma Research!
[Tuesday, August 3, 2010]
The Canine Hereditary Cancer Consortium (CHCC) needs
your help! They are studying canine melanoma and are
requesting blood samples from any purebred dog to
further their research to identify the underlying
genetic lesions and biochemical pathways that
contribute to this disease.
Melanoma is a form of cancer in which the
pigment-producing cells of the skin, melanocytes,
multiply in an uncontrolled manner. Canine melanoma
can be malignant or benign; malignant cancer is
capable of spreading from the original tumor to
lymph nodes and distant organs. Once melanoma is
established in an organ, additional tumors grow and
often ultimately cause the death of the animal.
Canine melanoma is frequently malignant when it
occurs in the mouth, toes or behind the eyes. Oral
melanoma, for example, is a particularly aggressive
subtype of the disease, with a 5-year survival rate
of 10 - 25%.
The CHCC will provide sample collection kits and pay
for shipping. Requested samples include whole
blood (5 mls in an EDTA "purple top" tube) and/or
fresh tumor samples. Dogs in remission are eligible
to participate in this study, as are dogs who have
already had tumors removed.
For further information, collection kits and
shipping information, please contactDr. Roe Froman
at the Van Andel Research Institute (office:
616.234.5569 cell: 616.914.0934).
The Canine Hereditary Cancer Consortium (CHCC),
headed by Drs. Jeff Trent (TGen), Nick Duesbery (Van
Andel Research Institute), and Paul Meltzer
(National Cancer Institute/NIH), is an unprecedented
alliance of scientists, veterinarians and
physicians. The melanoma research will be supported
by the recent approval of a 2-year, $4.3 million
federal stimulus grant to the CHCC, which includes
TGen and the Van Andel Research Institute in
partnership with the National Cancer Institute
(NCI), the University of Pennsylvania, Michigan
State University, dog breeders and veterinarians.
The AKC Canine Health Foundation, founded in 1995,
is the largest nonprofit worldwide to fund health
research exclusively for canines. Our goal is to
help dogs live longer, healthier lives. The AKC
Canine Health Foundation is the leader in
non-invasive genetic health research, stem cell
research, and biotherapeutics benefiting both
canines and humans. Through the generous
financial support of the American Kennel Club,
Nestlé Purina PetCare Co., and Pfizer Animal Health,
as well as thousands of clubs and individuals, we’re
proud to announce we have allocated nearly $24
million to canine health research at veterinary
schools and research institutions worldwide.
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Golden Retriever Foundation Partners with
Morris Animal Foundation to Help Dogs Live Longer
Healthier Lives
June 2, 2010/Denver/Overland Park, Kan.— The Golden
Retriever Foundation and Morris Animal Foundation
have teamed up to announce a new major canine
cancer study titled Discovery and Characterization
of Heritable and Somatic Cancer Mutations in Golden
Retrievers, or the MADGiC Project (Making Advanced
Discoveries in Golden Cancers). This is a
three-year, $1 million project slated to start in
the summer of 2010. This jointly funded project is
part of Morris Animal Foundation’s Canine Cancer
Campaign, a worldwide effort to prevent, treat and,
ultimately, cure this disease in dogs. Learn more
at CureCanineCancer.org <http://curecaninecancer.org/>.
The study will be led by premier canine cancer
researchers Jaime Modiano, VMD, PhD, at the
University of Minnesota; Matthew Breen, PhD, at
North Carolina State University; and Kerstin
Lindblad-Toh, PhD, at the Broad Institute of MIT and
Uppsala University, Sweden. They will work together
to investigate mutations that are involved in risk
and progression of the two most common cancers
affecting Golden Retrievers, hemangiosarcoma and
lymphoma. This research will be of interest to all
dog owners because these cancers affect every breed
and cause the deaths of tens of thousands of dogs
each year.
It is expected that this research may directly
benefit humans too, because the genes involved in
cancer are sometimes the same in dogs as in people,
although these mutations can be more difficult to
discover in people. Therefore, identifying these
genes may also advance scientists’ understanding of
common human cancers such as lymphoma.
In addition, researchers will seek to identify genes
that predispose some dogs to cancer so that breeders
may someday be able to reduce cancer risk through
breeding selection. DNA tests may also be used for
diagnosis and possibly to guide treatment choices in
the future. The scientists will also investigate
mutations that occur in the tumors themselves and
will profile the susceptibility of specific tumor
types to various chemotherapy compounds, which may
lead to improved therapy options.
Owners of Golden Retrievers diagnosed with lymphoma
or hemangiosarcoma can support this research by
donating a small tumor and/or blood sample; blood
samples from healthy Goldens over 12 years of age
are also needed. More information about sample
donation can be found at www.breenlab.org, www.modianolab.org,www.dogdna.orgor contact
Rhonda Hovan at rhondahovan@aol.comor 330-668-0044.
About The Golden Retriever Foundation http://www.goldenretrieverfoundation.org/
About Morris Animal Foundation http://www.morrisanimalfoundation.org/
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Read about the Animal Cancer Care and
Research (ACCR) programme's successes in Synergy.
Synergy is designed to provide you with information
about the research and treatment efforts of the
University of Minnesota College of Veterinary
Medicine's Animal Cancer Care and Research (ACCR)
programme and how these efforts may be of service to
you and the animals you care about. The ACCR
programme is part of the University of Minnesota
College of Veterinary Medicine and Masonic Cancer
Centre. Its mission is to advance knowledge in
cancer biology that can be translated and
implemented into treatment that will reduce the
incidence of cancer and improve the outcomes for
animals and humans with cancer.
http://www.cvm.umn.edu/accr/newsletters/home.html
The Animal Cancer Care and Research (ACCR) programme
brings together researchers from different
disciplines across human and veterinary medicine,
who strive to learn more about the area of cancer
where humans and animals interface. Their
discoveries lead to better ways to treat and prevent
cancers in both humans and animals. Research for the
ACCR programme is conducted primarily through three
university laboratories: The Modiano Lab, the Kassie
Lab, the O'Brien Lab, and the St. Hill Lab.
The mission of the Animal Cancer Care and Research
(ACCR) programme is to advance knowledge in cancer
biology that can be translated and implemented into
delivery of care that will reduce the incidence of
cancer and improve the outcomes for animal and human
cancer patients.
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The AKC Canine Health Foundation
is pleased to announce funding for
two grants that are expected to improve therapies to treat canine
lymphomas. Lymphoma is the most commonly seen cancer in dogs.
Typically, animal treatment protocols are not based on scientific
research; rather, information from human studies are extrapolated to
veterinary medicine. Veterinarians often determine what protocol to
use based on their past experiences and the experiences of their
colleagues. The two studies listed below look to generate scientific
evidence on how the drugs of current standards of care actually affect
lymphoma cells, thereby providing evidence-based recommendations for
canine lymphoma treatments.
Grant 1226-A: Evalution of Multidrug Resistance Genes in Primary
Canine Lymphoma Cells Exposed to Enrofoxacin and Prednisolone was
recently approved for $7,190 to Dr. Annette N. Smith at Auburn
University in Alabama. This research seeks to evaluate the expression
of the drug resistance gene, MDR1, in lymphoma cells in response to
exposure to treatment with an antibiotic or corticosteroid. Over-
expression of this gene has been associated with a poor prognosis and
a decreased survival time due to the lack of response to treatment. If
these two treatments (the antiobiotic and cortisosteroid) do in fact
trigger the expression of MDR1, the management (treatment) of clinical
patients with lymphoma should change.
Grant 1344-A: Comparison of Percentage of T Regulatory Cells in Dogs
with Spontaneoudsly Occurring Lymphoma Following Oral Versus
Intravenous Cyclophosphamide was approved for $12,852 to Dr. Kimberly
A. Selting at the University of Missouri, Columbia. A subset of immune
cells called T regulatory cells (Tregs) determines what cells belong
in your body. Tregs can prevent other immune cells from affecting
cancer in the body, and are therefore thought to be detrimental to the
body's ability to fight off cancer. This study will characterize the
population of Tregs in dogs with lymphoma before they are treated, and
then after they receive cyclophosphamide. Researchers will also
compare injected to oral cyclophosphamide. No study has ever
appropriately compared these two ways to give cyclophosphamide to
decide which is better. By considering the effects on Tregs, the side
effects and the efficacy, researchers will be able to recommend the
best way to use this drug.
The AKC Canine Health Foundation has funded 27 grants valued at more
than $1.7 million dealing with more effective treatments and the
genetics of lymphoma. Through this research there may one day be a way
to prevent or cure this cancer that affects the entire canine community.
To donate to canine health research or to learn more visit
www.akcchf.org
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FDA NEWS RELEASE
For Immediate Release: June 3, 2009
FDA: First Drug to Treat Cancer in
Dogs Approved The U.S. Food and Drug
Administration today announced the approvalof
Palladia (toceranib phosphate), the first drug
developedspecifically for the treatment of cancer in
dogs.
Palladia is approved to treat
canine cutaneous (skin-based) mastcell tumors, a
type of cancer responsible for about 1 out of 5
casesof canine skin tumors. The drug is approved to
treat the tumors withor without regional lymph node
involvement.
All cancer drugs now used in
veterinary medicine originally weredeveloped for use
in humans and are not approved for use in
animals.Cancer treatments used in animals are used
in an “extra-label”manner as allowed by the Animal
Medicinal Drug Use Clarification Actof 1994.
"This cancer drug approval for
dogs is an important step forward forveterinary
medicine," said Bernadette Dunham, D.V.M.,
Ph.D.,director of FDA's Center for Veterinary
Medicine. "Prior to thisapproval, veterinarians had
to rely on human oncology drugs, withoutknowledge of
how safe or effective they would be for dogs.
Today'sapproval offers dog owners, in consultation
with their veterinarian,an option for treatment of
their dog's cancer."
While canine mast cell tumors
often appear small and insignificant,they can be a
very serious form of cancer in dogs. Some mast
celltumors are easily removed without the
development of any furtherproblems, while others can
lead to life threatening disease.
Palladia is a tyrosine kinase
inhibitor and works in two ways: bykilling tumor
cells and by cutting off the blood supply to
thetumor. In a clinical trial, Palladia showed a
statisticallysignificant difference in tumor
shrinkage when compared with aninactive substance
(placebo).
The most common side effects
associated with Palladia are diarrhea,decrease or
loss of appetite, lameness, weight loss, and blood
inthe stool.
Palladia is manufactured by Pfizer
Animal Health Inc., New York City.
********************
For more information, check out:
http://vetmedicine.about.com/b/2009/06/03/palladia-new-anti-cancer-drug-for-dogs.htm
Freedom of Information Summary --
Original New Animal Drug Application
Palladia -- toceranib phosphate
tablets for dogs -- approved May 22,2009
For the treatment of Patnaik grade
II or III, recurrent, cutaneousmast cell tumors with
or without regional node involvement in dogs--
Sponsored by Pharmacia & Upjohn Company, a Division
of Pfizer, Inc.
********************
http://vetmedicine.about.com/b/2009/06/03/palladia-new-anti-cancer-drug-for-dogs.htm
Janet's Veterinary Medicine Blog'
Janet Tobiassen, DVM
********************
http://www.palladia-pi.com/Palladia_PI.pdf
Palladia Client Information Sheet
********************
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http://grca.org/pdf/health/healthsurvey.pdf
Deciding Whether and When to
Neuter a Golden Retriever
Faera
Rhonda Hovan
A focus on the serious issues of
pet overpopulation and unwanted puppies has led to
the common practice of neutering dogs prior to
sexual maturity, often near the age of six months.
While this clearly helps reduce unplanned breedings
and thereby may serve the public interest, research
is increasingly showing that it may not be in the
best health interests of an individual dog with a
responsible owner. Breeds of dogs vary considerably
with regard to their rate of maturity and risk for
specific diseases, and the interaction of these
factors with natural hormones should properly be
taken into consideration when deciding whether and
when to neuter a dog. However, appropriately
tailoring neutering recommendations to a breed
requires awareness of the ways in which neutering
and the age of neutering affect specific breeds, and
it may be impossible for veterinarians to know this
in detail for every breed.
Therefore, below is a review of
health consequences to consider when deciding
whether and/or when to neuter a Golden Retriever.
The term “Golden” will be used when the data are
specific to Goldens, and most of this data come from
a large breed health survey scientifically conducted
and analyzed by a veterinary epidemiologist () The
term “dogs” will be used when the data are
applicable to many breeds, and supporting references
are provided. In some cases the findings have been
substantiated across many breeds, but relative risk
is also defined specifically for Goldens. The term
“neuter” refers to either sex.
Please note that there are both
health benefits and detriments associated with
neutering and various neutering ages, so decisions
will need to balance these complex factors. It is
relevant to consider what diseases are more and less
common in the breed, and also what diseases have
greater or lesser consequences to the dog, so that
information is also provided. For example, it is
important with reference to cancer risk to know that
18% of all Goldens die from hemangiosarcoma but that
testicular cancer is rare (less than ½ of 1%), so
that appropriate weight can be given to the effect
that neutering has on each of those cancers.
Health Consequences Associated
with Neutering and the Age of Neutering
-
Neutered dogs have a higher
incidence of hypothyroidism than do intact dogs.
Male Goldens neutered prior to one year of age
have an 80% increased risk of hypothyroidism and
female Goldens neutered prior to one year of age
have a 60% increased risk of hypothyroidism, as
compared to those neutered after one year of age
or not neutered. Hypothyroidism is a common but
treatable disease in the breed.
-
Neutered dogs have a greater
incidence of hip dysplasia and torn cruciate
ligaments than intact dogs, and there is some
evidence to suggest that this risk is most
pronounced in dogs neutered prior to sexual
maturity. Hip dysplasia is common in Goldens,
and torn cruciate ligaments are less common but
not rare. Both of these diseases can be treated
surgically, but treatment is costly and success
is variable depending on many factors.
-
There is some evidence that
the incidence of cardiac hemangiosarcoma is
greatly increased (2-5 times) in neutered dogs,
and that the risk of splenic hemangiosarcoma may
also be increased in neutered dogs.
Hemangiosarcoma is the most common cancer in the
breed, causing the death of approximately 1 in 5
Goldens. Most of these tumors occur in the
spleen, with fewer but still a substantial
number in the heart. This is a rapidly
progressing and incurable cancer.
-
Several studies indicate that
the incidence of osteosarcoma (bone cancer) is
significantly higher in neutered dogs than in
intact dogs, but there is some evidence that
this increase is not as great when neutering
occurs after sexual maturity. This cancer
affects about 5% of Goldens, and is not curable.
-
Dogs neutered prior to sexual
maturity grow taller than their natural genetic
potential, and their bone structure is altered
toward a more narrow, lanky appearance. Taller
Goldens have shorter life spans than shorter
Goldens. Among male Goldens, the shortest males
live 2.2 years longer than the tallest males;
and among female Goldens, the shortest females
live 1.1 years longer than the tallest females.
It is unlikely that neutering a Golden prior to
sexual maturity will alter the dog’s potential
height from extremely short to extremely tall,
but it will make a noticeable difference in
height and thus potentially in life span.
-
Neutered females have a
greatly increased risk of urinary incontinence
as compared to those not neutered, but there is
some evidence that this increased risk is less
significant for dogs neutered after sexual
maturity. Urinary incontinence is neither common
nor rare in Goldens, and can often (but not
always) be treated successfully.
-
Females neutered prior to
their first heat cycle have less than ½ of 1%
chance of developing mammary cancer (breast
cancer). In females neutered after the first
cycle but before the second, this risk increases
to 4%. And if a female is not neutered until
after her second heat cycle, this risk increases
to about 13%. If detected early through regular
mammary exams, most but not all mammary cancers
can be treated successfully with surgery and
sometimes additional therapies.
-
Males with one or more
testicles located in the abdomen
(cryptorchidism) are at high risk for testicular
cancer and should be neutered prior to 15 months
of age, which eliminates this risk. It is not
necessary to neuter these dogs prior to sexually
maturity to avoid testicular cancer. Testicular
cancer is rare (less than ½ of 1%) in dogs with
both testicles normally descended into the
scrotum.
-
Females that remain intact are
exposed to a significant risk for pyometra (a
life threatening uterine infection) that rises
with every heat cycle, particularly after the
age of five years. Pyometra is a common and
rapidly progressing disease in Goldens that must
be diagnosed promptly to be successfully
treated.
-
Males that remain intact
frequently develop an enlarged prostate gland
(benign prostatic hyperplasia) as they age,
particularly over the age of seven years. This
is not a serious disease, and while it can
sometimes be managed medically, neutering
affected dogs is curative. This is not to be
confused with prostate cancer which is uncommon
in the breed, although more common in neutered
males than intact males.
Taking all of the above factors
into consideration, there is good evidence to
support that it is in the best overall health
interests of the dog to neuter female Goldens after
sexual maturity, at approximately one year of age.
This typically allows a female to have one heat
cycle but not two, which keeps the risk of mammary
cancer low while still providing her with some
important health benefits gained by maturing with
natural hormones. Of course, the female must be kept
on leash or securely fenced away from males for the
full three weeks of her heat cycle to avoid unwanted
pregnancy, so this should not be undertaken unless
the owner is able to be certain that there is no
possibility of an accidental breeding.
There are no clear significant
health benefits to neutering a normal male, so this
decision should be based on factors other than the
health of the dog, such as preventing unwanted
breedings, reducing the risk of male-to-male
dominance/aggression, and reducing roaming behavior
and urine marking. If a male is going to be
neutered, there is good evidence to support that it
is in the overall best health interests of the dog
to neuter male Goldens after sexual maturity, at
approximately one year of age. Neutering a male
after two years of age has less impact on behavior,
so if behavioral considerations are important to the
owner, neutering should be done prior to the age of
two.
References
Arnold S. Urinary incontinence in
castrated bitches. Part I. Significance, clinical
aspects and etiopathogenesis. Schweiz Arch
Tierheilkd 1997;139:271-276.
Berry SJ, Strandberg JD, Saunders
WJ, et al. Development of canine benign prostatic
hyperplasia with age. Pros 1986;9:363-373.
Bryan JN, Keeler MR, Henry CJ, et
al. A population study of neutering status as a risk
factor for canine prostate cancer. Pros
2007;67:1174-1181.
Cooley DM, Beranek BC, Schlittler
DL, et al. Endogenous gonadal hormone exposure and
bone sarcoma risk. Canc Epidemiol Biomark Prev
2002;11:1434-1440.
Duerr FM, Duncan CG, Savicky RS,
et al. Risk factors for excessive tibial plateau
angle in large-breed dogs with cranial cruciate
ligament disease. J Amer Vet Med Assoc
2007;231:1688-1691.
Egenvall A, Hagman R, Bonnett BN,
et al. Breed risk of pyometra in insured dogs in
Sweden. J Vet Intern Med 2001;15:530-538.
Hart BL, Eckstein RA. The role of
gonadal hormones in the occurrence of objectionable
behaviours in dogs and cats. Appl Anim Behav Sci
1997;52:331-344.
Howe LM, Slater MR, Boothe HW, et
al. Long-term outcome of gonadectomy performed at an
early age or traditional age in dogs. J Amer Vet Med
Assoc 2001;218:217-221.
Kustritz MV. Determining the
optimal age for gonadectomy of dogs and cats. J Am
Vet Med Assoc. 2007 Dec 1;231(11):1665-75.
Nielsen JC, Eckstein RA, Hart BL.
Effects of castration on problem behaviors in male
dogs with reference to age and duration of behavior.
J Amer Vet Med Assoc 1997;211:180-182.
Niskanen M, Thrusfield MV. Associations between age,
parity, hormonal therapy and breed, and pyometra in
Finnish dogs. Vet Rec 1998;143:493-498.
Panciera DL. Hypothyroidism in
dogs: 66 cases (1987-1992). J Amer Vet Med Assoc
1994;204:761-767.
Prymak C, McKee LJ, Goldschmidt
MH, et al. Epidemiologic, clinical, pathologic, and
prognostic characteristics of splenic
hemangiosarcoma and splenic hematoma in dogs: 217
cases (1985). J Amer Vet Med Assoc 1988;193:706-712.
Ru G, Terracini B, Glickman LT, et
al. Related risk factors for canine osteosarcoma.
Vet J 1998;156:31-39.
Salmeri KR, Bloomberg MS, Scruggs
SL, et al. Gonadectomy in immature dogs: effects on
skeletal, physical and behavioral development. J
Amer Vet Med Assoc 1991;198:1193-1203.
Slauterbeck JR, Pankratz K, Xu KT,
et al. Canine ovariohysterectomy and orchiectomy
increases the prevalence of ACL injury. Clin Orthop
2004;429:301-305.
Sorenmo K. Canine mammary gland
tumors. Vet Clin NA 2003;33:573-596.
Spain CV, Scarlett JM, Houpt KA.
Long-term risks and benefits of early-age
gonadectomy in dogs. J Amer Vet Med Assoc
2004;224:380-387.
Teske E, Naan EC, VanKijk EM, et
al. Canine prostate carcinoma: epidemiological
evidence of an increased risk in castrated dogs. Mol
Cell Endo 2002;197:251-255.
van Hagen MA, Ducro BJ, van den
Broek J, Knol BW. Incidence, risk factors, and
heritability estimates of hind limb lameness cause
by hip dysplasia in a birth cohort of boxers. Am J
Vet Res. 2005 Feb;66(2):307-12.
Verstegen J, Onclin K.
Etiopathogeny, classification and prognosis of
mammary tumors in the canine and feline species.
Proceedings, Society for Theriogenology,
2003:230-238.
Ware WA, Hopper DL. Cardiac tumors
in dogs: 1982-1995. J Vet Intern Med 1999;13:95-103.
PO Box 1110 • Bath, OH • 44210
Phone: 330-668-0044 • Cell: 330-338-4236
rhondahovan@aol.com
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Dr. Rona Sherebrin,
DVM, CVA
Secord Animal Hospital
3271 Yonge St.
Toronto, ON
M4N 2L8
416-486-1700
Cell 416-274-3366
www.myTCMvet.com
Follow me on Twitter! Username: TCMVET
Screenshot of
article
full article posted
on TheStar.com at (
http://www.thestar.com/article/666233 )
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University of Minnesota
Office of the Dean
College of Veterinary Medicine
Dear colleague:
Exciting discoveries are occurring every day at the
College of Veterinary Medicine, and I would like to
tell you about one of the most far-reaching that has
resulted from our research. In fact, you may have
already heard about it.
In August 2008, Batman, a pointy-eared German
shepherd mixed-breed dog with a fatal form of brain
cancer, underwent a breakthrough, life-saving
procedure developed by University of Minnesota
surgeons and scientists at the College of Veterinary
Medicine and School of Medicine. Without this novel
procedure, chances are Batman would not have lived
past Halloween. Today, he is still a tail-wagging
companion, full of energy and with no sign of tumor
recurrence.
What is even more amazing, though, is that this
treatment is now available on a clinical-trial basis
to other dogs with brain cancer. If the results of
these clinical trials are as promising as we
suspect, the revolutionary new treatment protocol
may one day be used to treat other types of cancer
in dogs. It could even be tested in human trials in
the near future, with the ultimate goal of curing
brain cancers in people like Sen. Ted Kennedy.
Most of the credit for this new treatment procedure
goes to G. Elizabeth Pluhar, D.V.M., Ph.D., and John
Ohlfest, Ph.D. Their revolutionary three-pronged
approach to treatment consists of surgically
removing the tumor; treating the surgical site with
a form of gene therapy to attract immune cells that
will recognize and destroy remaining tumor cells;
and administering an anti-cancer vaccine made from
the dog’s own cancer cells to prevent the tumor from
recurring.
To date, five dogs have received the treatment with
promising results, and we are now formally opening
the clinical trials to other dogs with primary brain
tumors. Treatment will occur through the canine
brain tumor clinical trials program. The trial team
currently has funding to treat up to 50 dogs, but
that number could soon exceed 100 if additional
grants and charitable donations come through.
With this in mind, I am asking your help in
referring canine patients that you think could
benefit from this program. Please see the enclosed
brochure with information about the program and a
link to our Web site, where you or any referring
veterinarian can submit a request to enroll a dog in
this study. Please share it with pet owners whose
dogs may benefit from this effort while helping our
study.
Treatment is expensive; the cost of therapy for one
dog can reach $20,000. The canine brain tumor
clinical trials program, however, will cover the
vast majority of treatment costs while a dog remains
in a trial. Owners are responsible only for the
costs of diagnostic tests, and even these can be
waived under specific circumstances.
The far-reaching implications of this promising new
treatment are almost difficult to fathom; not only
could these treatments lead to a cure for brain and
other systemic cancers in dogs, but because dogs and
humans share many physiological traits, dogs could
also be the missing link in the cure for brain
cancer in humans.
Learn more about the trials and apply for the
program online at www.cvm.umn.edu. To schedule a
brain scan, call 612-625-8755 or 612-626-8387 for an
appointment with Dr. Pluhar or the Small Animal
Surgery or Neurology Service. To donate to the
research effort, click here and select new gift,
then designate the gift is for the CVM canine brain
tumor clinical trials effort. Or you can contact
Sharon Staton, director of advancement, at
612-624-1247, or e-mail her atstato001@umn.edu.
Sincerely,
Trevor Ames, D.V.M., M.S.
Diplomate ACVIM
Dean
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Northern Colorado Business Report
December 19, 2008
CANCER DIAGNOSTIC TOOL
MOVES TOWARD MARKET
FORT COLLINS - Colorado
State University and NeoTREX, the private enterprise
arm of the university's cancer Supercluster, have
inked a license agreement with the Veterinary
Diagnostic Institute of Irvine, Calif., covering a
cancer detection test for dogs.
Under the
agreement, the technology co-invented by faculty
members at CSU's renowned Animal Cancer Center and
scientists at the California lab will be
commercialized and marketed by the diagnostic
institute.
The simple blood test measures
levels of a special enzyme that suggests a dog might
have hemangiosarcoma, a cancer that occurs mostly in
large-breed dogs over the age of 8. The cancer can
result in internal hemorrhage leading to death.
Ultrasound is the only other diagnostic tool used
for the detection of the cancer.
Nearly half
of the 75 million pet dogs older than 10 in the
United States will die from cancer. The Veterinary
Diagnostic Institute will market the hemangiosarcoma
test along with another that detects lymphoma in
dogs.
NeoTREX translates CSU research
discoveries into products that aid in the
prevention, diagnosis and treatment of cancer. The
agency is a division of the nonprofit CSU Ventures
Inc.
The university's cancer Supercluster is
a multi-disciplinary group of faculty members from
across various campus departments who are engaged in
cancer research. |
|
Golden Retriever Familial Subaortic Stenosis
Study
Dr. Joshua Stern and the Cardiac Genetics
Laboratory of Washington State University College of
Veterinary Medicine are conducting a research study
to identify the genetic mutation responsible for
Subvalvular Aortic Stenosis (SAS) in Golden
Retrievers. Advancements in technology have enabled
us to become increasingly successful in identifying
mutations responsible for breed specific heart
disease and to develop DNA tests to help breeders
reduce the incidence of disease.
This study requires DNA samples from 30 Golden
Retrievers with a diagnosis of Subvalvular aortic
stenosis (diagnosed by Doppler echocardiogram) and
an additional 30 Goldens without Subvalvular aortic
stenosis (as cleared by a cardiologist).
Participants can be assured that their privacy will
be protected and confidentiality maintained..
Your participation is greatly appreciated and
questions are welcome!.
Please complete the form on page 2 and return
along with the sample and required cardiologist
report and pedigree to:
VCGL – WSU
Post Office Box 605
Pullman, WA 99163-0605
Sample collection
1. Please draw 2-3 ml of blood into an EDTA tube
(lilac top). Most veterinary hospitals have these
readily available, and many veterinarians are
willing to waive their professional fee when
obtaining samples for research purposes.
2. Please label tube well with dog’s call name and
family last name.
3. Although this is not required for participation
in the current study, ideally we would like to also
bank DNA from Goldens affected with SAS in the CHIC
DNA Repository for use in future research studies.
If you are willing to do this, please download and
complete both the Application form and the Health
Survey from
http://www.caninehealthinfo.org/dnabank.html and
include both forms with sample. There is no fee for
doing this.
The blood does not need to be mailed with ice
packs or be shipped overnight. However, please try
to send the sample within a few days by standard
mail. Until the blood can be mailed, please keep it
refrigerated (i.e., if the blood was drawn late
Saturday and cannot be mailed until Monday, please
refrigerate between Saturday and Monday).
Questions? Email:
jsterndvm@gmail.com Phone: 614.390.1516
Right click on the link, and
select 'Save As' to download the PDF document.
Golden
Retriever Familial Subaortic Stenosis Study
Thank you very much for submitting
a sample, we greatly appreciate it! |
|
FDA NEWS RELEASE
For Immediate Release: June 3, 2009
FDA: First Drug to Treat Cancer in Dogs Approved
The U.S. Food and Drug Administration today
announced the approval of Palladia (toceranib
phosphate), the first drug developed specifically
for the treatment of cancer in dogs.
Palladia is approved to treat canine cutaneous
(skin-based) mast cell tumors, a type of cancer
responsible for about 1 out of 5 cases of canine
skin tumors. The drug is approved to treat the
tumors with or without regional lymph node
involvement.
All cancer drugs now used in veterinary medicine
originally were developed for use in humans and are
not approved for use in animals. Cancer treatments
used in animals are used in an “extra-label” manner
as allowed by the Animal Medicinal Drug Use
Clarification Act of 1994.
"This cancer drug approval for dogs is an important
step forward for veterinary medicine," said
Bernadette Dunham, D.V.M., Ph.D., director of FDA's
Center for Veterinary Medicine. "Prior to this
approval, veterinarians had to rely on human
oncology drugs, without knowledge of how safe or
effective they would be for dogs. Today's approval
offers dog owners, in consultation with their
veterinarian, an option for treatment of their dog's
cancer."
While canine mast cell tumors often appear small and
insignificant, they can be a very serious form of
cancer in dogs. Some mast cell tumors are easily
removed without the development of any further
problems, while others can lead to life threatening
disease.
Palladia is a tyrosine kinase inhibitor and works in
two ways: by killing tumor cells and by cutting off
the blood supply to the tumor. In a clinical trial,
Palladia showed a statistically significant
difference in tumor shrinkage when compared with an
inactive substance (placebo).
The most common side effects associated with
Palladia are diarrhea, decrease or loss of appetite,
lameness, weight loss, and blood in the stool.
Palladia is manufactured by Pfizer Animal Health
Inc., New York City.
For more information:
Palladia approval summary |
|
U OF M COLLEGE OF VETERINARY MEDICINE INTRODUCES
COLLABORATIVE CANCER PROGRAM
MINNEAPOLIS/ST. PAUL (February 27, 2009) – The
University of Minnesota College of Veterinary
Medicine, in conjunction with the University’s
Masonic Cancer Center, is has established a new
Animal Cancer Care and Research (ACCR) program.
This collaboration is unique in the United States
because it incorporates the ACCR program into the
Masonic Cancer Center, one of only 41 National
Cancer Institute-designated Comprehensive Cancer
Centers in the United States.
“We believe it will become the premier model for
animal cancer care and research,” says Dr. Trevor
Ames, dean of the College of Veterinary Medicine.
Within five years Ames says he expects the
University of Minnesota to be recognized as the best
institution in the country for conducting research
in comparative oncology and providing care for
companion animals with cancer.
“ACCR scientists have already made significant
discoveries,” says Ames. “One particularly
noteworthy finding is that many cancers in the dog
are caused by the same genetic abnormalities found
in humans.”
The mission of the ACCR program is ambitious: To
advance knowledge in cancer biology that can be
translated and implemented into treatment that will
reduce the incidence of cancer and improve the
outcome for animal and human cancer patients.
“The ACCR program is a key part of our Comparative
Medicine Signature Program at the University,” says
Dr. Robert Washabau, who chairs the Department of
Veterinary Clinical Sciences. “Cancer claims the
lives of animals as well as humans, and research
into the causes and treatments of cancer is often
applicable across species.”
The ACCR program draws its expertise primarily from
scientists in the College of Veterinary Medicine and
the Masonic Cancer Center, but ACCR scientists also
work closely with the Medical School, School of
Pharmacy, and School of Public Health.
“Great synergies can be achieved when
veterinarians, physicians, and scientists with
complementary expertise join forces to tackle the
types of cancer shared by dogs and humans,” says Dr.
Jaime Modiano, director of the ACCR program. “ACCR
researchers are currently working to define breed-
and disease-specific ‘Achilles’ heels’ in dogs.
These findings could then be translated into more
effective and less toxic cancer treatments. The
implications could reach far beyond dogs and
veterinary medicine.”
Modiano’s laboratory is one of three research
labs involved in the program. Modiano holds the
Alvin S. and June Perlman Endowed Chair in Animal
Oncology and is a member of the Masonic Cancer
Center’s Genetic Mechanisms of Cancer and Immunology
research programs.
ACCR scientists work on research in genetics,
cancer prevention, stem cells, metastasis, and cell
signaling. Many of these basic research findings are
readily translated into cancer care including
diagnostics, treatments, and quality of life.
“We can learn more about cancer by working
together,” says Douglas Yee, M.D., director, Masonic
Cancer Center. “This program will advance our
understanding of cancer in both animals and people.”
For more information on the Animal Cancer Care
and Research program please see the attached
newsletter, Synergy, or to download a PDF of the
ACCR newsletter, Synergy, go to
www.cvm.umn.edu/accr. |
Using naturally occurring tumours in dogs and
cats to study telomerase and cancer stem cell
biology.
Pang LY,
Argyle DJ.
Hospital for Small Animals, Royal (Dick) School of
Veterinary Studies and the Roslin Institute,
University of Edinburgh, Easter Bush, Midlothian
EH25 9RG, Scotland, UK.
The recently described cancer stem cell theory opens
up many new challenges and opportunities to identify
targets for therapeutic intervention. However, the
majority of cancer related therapeutic studies rely
upon rodent models of human cancer that rarely
translate into clinical success in human patients.
Naturally occurring cancers in dogs, cats and humans
share biological features, including molecular
targets, telomerase biology and tumour genetics.
Studying cancer stem cell biology and
telomere/telomerase dynamics in the cancer bearing
pet population may offer the opportunity to develop
a greater understanding of cancer biology in the
natural setting and evaluate the development of
novel therapies targeted at these systems.
Biochim Biophys Acta. 2009 Apr;1792(4):380-91. Epub
2009 Feb 28. |
Translation of new cancer treatments from pet
dogs to humans.
Paoloni M,
Khanna C.
Comparative Oncology Program, Center for Cancer
Research, National Cancer Institute, 37 Convent
Drive, Room 2144, Bethesda, Maryland 20892, USA.
Naturally occurring cancers in pet dogs and humans
share many features, including histological
appearance, tumour genetics, molecular targets,
biological behaviour and response to conventional
therapies. Studying dogs with cancer is likely to
provide a valuable perspective that is distinct from
that generated by the study of human or rodent
cancers alone. The value of this opportunity has
been increasingly recognized in the field of cancer
research for the identification of cancer-associated
genes, the study of environmental risk factors,
understanding tumour biology and progression, and,
perhaps most importantly, the evaluation and
development of novel cancer therapeutics.Nat Rev
Cancer. 2008 Feb;8(2):147-56 |
Oncology of companion animals as a model for
humans. an overview of tumor histotypes.
Porrello A,
Cardelli P,
Spugnini EP.
Molecular Oncogenesis Laboratory, Regina Elena
Cancer Institute, Rome, Italy.
The need for more appropriate animal models in
cancer research has led, over the past 20 years, to
consider pets with spontaneously occurring neoplasms
as a valuable and still under used resource. The
role of companion animals in the struggle to
eradicate cancer can be multiple: they may act as
environmental sentinels, help in gaining insights on
tumor biology and finally may be enrolled in
therapeutic trials which might act as a bridge to
the clinic applications. This paper will focus on
the most valuable spontaneous neoplasms in companion
animals and will analyze the potentials of each
histotype as a model for basic research and for new
therapeutic strategies. It is conceivable that in
the next years comparative oncology will play a
paramount role in translational medicine allowing a
rapid flow of data from laboratories to clinical
application in humans.J Exp Clin Cancer Res. 2006
Mar;25(1):97-105 |
Using the canine genome to cure cancer and
other diseases.
Olson PN.
Morris Animal Foundation, 45 Inverness Drive East,
Englewood, CO 80112, USA.
polson@morrisanimalfoundation.org
A high-quality draft genome sequence of the domestic
dog (Canis familiaris), together with a dense map of
single nucleotide polymorphisms, has been reported.
Such new tools offer scientists amazing
opportunities to define genetic, nutritional,
environmental, and other risk factors for various
canine diseases. Because many of the diseases that
affect man's best friend also affect us,
understanding a dog's disease may lead to new
preventions and therapies for diseases that affect
both dogs and people. Since a dog's life span is
shorter than that for a human, monitoring potential
risk factors in a well-controlled population of dogs
is possible. Such a population should be one where
dogs live in close relationship with their owners.
Although longitudinal studies have been previously
conducted on animals housed in laboratory
environments, the natural environment offers a
chance to study dogs in environments shared by their
owners. If dogs are carefully monitored, and select
exposures defined, considerable information could be
collected in a dog's lifetime--the next 10-20 years.
Such information could hold the clues for important
discoveries, including causes and cures for cancer.
Theriogenology. 2007 Aug;68(3):378-81. Epub 2007 May
10. |
Love/Avon Army of Women is a charitable services fund of the Dr. Susan Love Research Foundation, 1 501(c)(3) tax-exempt organization. Your support will enable them to recruit one million women to sign up on to the Love/Avon Army of Women and participate in simple but vital breast cancer research. The Army of Women will expand breast cancer prevention research in new directions ~ moving us beyond a cure, to understanding what causes breast cancer and how to stop it one and for all.
To My Friends & Family,
As we near the beginning of a new year, I would like to share my wish for our future, and ask that you join me in helping to make it happen. It is rare for me to send a mass emailing, but this is a message that I believe should reach as many people as possible, so please forgive my use of blind copies (and you have my permission and request to forward).
While many of you know of my impassioned fight against canine cancer, I never forget that cancer is also the second leading cause of death in humans. Although it has been over thirty years since President Nixon declared "war on cancer," 1 in 4 of us will still die from cancer. So as important as the advances since that time have been, there is still much more to do. And that's where you come in -- and no, I am not asking for money.
One of the factors that frequently limits scientists' ability to study cancer is difficulty in recruiting people to participate. To address this need, a wonderful collaboration between the Dr. Susan Love Research Foundation and the Avon Foundation has embarked on a project called the Army of Women, with the goal of recruiting one million women to participate in cancer research. The primary goal of this project is to move beyond searching for cures to focus on prevention. While this project is aimed specifically at breast cancer, the information learned will undoubtedly move the whole field of cancer prevention forward.
The Army of Women project asks women to sign up by providing some very basic information such as email, phone number, address, and age, but they do not ask for any specific participation commitments. Once a person is signed up, they will receive periodic emails informing them of studies that are recruiting participants. These studies may be as simple as questionnaires about dietary and exercise habits, or may include other kinds of medical history and lifestyle considerations. Some studies may go further and request blood samples or other personal participation. But there is NEVER any pressure to participate, so please don't be hesitant to sign up -- you will not be asked to do anything you don't want to do. You will decide what you want to do or don't want to do, and can respond or not as you wish.
The Army of Women needs volunteers with all backgrounds -- those who have never had any cancer and those who have; those who have a family history and those who do not; those with no risk factors and those with known risk factors; all ages and all ethnic groups. In a word, they need everyone. If we want them to help us, we have to help them. And although the men in our life cannot sign up, it is very likely that they will benefit from these research projects too because factors involved in cancer prevention can often be generalized. (And that means that maybe our dogs will benefit too.)
So...thank you for letting me share my wish with you, and for considering this request. If you would like to learn more, or to sign up, please go to http://www.armyofwomen.org/ I would also be happy to talk with anyone personally about this.
Best,
Rhonda Hovan
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= 
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|
Be part of this study without
even leaving the house!
|
|
Dear,
Have you been diagnosed
with breast cancer? Whether you were
recently diagnosed, are in active
treatment, or are a long-term survivor,
you can participate in this online study
from the comfort of your own home!
With increased breast cancer survival
rates, it is more important than ever to
look at quality of life and how women
are coping during diagnosis, treatment,
and remission. If you have had breast
cancer and want a way to help
researchers find the answers to these
very important questions, consider
taking this online survey! If this study
isn't a right fit for you, you know what
to do...PASS IT ON!
|
What’s the study
about?
The purpose of
this study is to assess how
having had breast cancer affects
different aspects of a woman’s
life.
What’s involved?
If you join the
study, you will be asked to
answer a series of questions in
an ONLINE survey. You will
access the survey online from
your own computer. If you choose
the "yes, sign me up" option,
you will be taken to a page that
asks a few short screening
questions. If after you answer
the questions you are found to
be a match,you will be provided
a link to the online survey. You
will also be sent an e-mail that
contains the link to the on-line
survey so that you may access it
at a later time. You will only
need to take the survey once. In
order to ensure receipt of the
email, please remember to add info@armyofwomen.org to
your contact or safe-sender
list.
The questions asked in the
survey are related to medical
history, physical well-being,
social well-being, and emotional
well-being. The site is secure
and your participation is
anonymous. The survey is in
English and will take
approximately 45 minutes to
complete.
Who can
participate?
You can join the
Online Study on Breast Cancer
and Well-Being if you match ALL
of these categories:
• You are a woman who has been
diagnosed with breast cancer at
some point in her life
• Your breast cancer has not
metastasized (i.e., has not
spread beyond your breasts and
lymph nodes to any other organ
in your body)
• Aside from treatment for
breast cancer, you have never
received chemotherapy, hormone
therapy, or radiation therapy to
treat A DIFFERENT CANCER
Who is conducting
the study?
Catherine
Bielajew, PhD and Isabelle Ares,
PhD Candidate, University of
Ottawa, Ontario, Canada
Where?
Anywhere in the
world where there is internet
access
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An Important Message From the GRCA Health & Genetics Committee
The next issue of the "Golden Retriever News" will
present an update provided by the University of
Minnesota on research supported in part by the
Golden Retriever Foundation through its partnership
with the AKC Canine Health Foundation. Many GRCA
members donated blood and tumor samples in support
of this project, and we hope that knowing their dog
contributed to knowledge that will improve the
future for both humans and dogs will help these
owners to find meaning in their loss.
The results of this project were so impressive that
it caught the attention of the National Institutes
of Health, which has now contributed over one
million dollars to a subsequent project that will
build upon these findings. Therefore, we renew our
call to owners to participate in this research by
considering sample donation. While we continue to
also recruit samples for other studies and other
kinds of cancer (including blood from any affected
dog, even after beginning chemotherapy), this
particular project requires blood and tumor samples
from Goldens with lymphoma. Tumor samples must be
collected prior to beginning chemotherapy, and must
be prepared for shipment in a special transport
media which is overnighted to your veterinarian.
Therefore, it is critical that owners contact us
without delay when they even suspect their dog may
have lymphoma – it is not necessary for the
diagnosis to have been confirmed.
If you feel enlarged lymph nodes (for example,
“lumps” on the throat under the back of the jaw that
seemed to appear very rapidly), please contact us
even prior to your vet appointment if there is time
to do so. Or if your veterinarian has diagnosed
lymphoma based on a fine needle aspirate in the
office, please contact us immediately without
waiting for a pathology report or oncology
consultation.
Please use any of the following contacts:
Tessa Breen (sample coordinator for Dr Matthew
Breen)
Tessa_Breen@ncsu.edu
919-513-1466
The Modiano Lab
lab@modianolab.org
612-626-6890
Rhonda Hovan (GRCA Research Facilitator)
rhondahovan@aol.com
330-668-0044 hm or 330-338-4236 cell
Thank you again for your past support, and in
advance for your future support. As you will read in
the GRNews, by working together, we are making a
difference!
Cross-posting is permitted and encouraged.
|
| Centre for Companion Animal Health
UC Davis School of Veterinary Medicine
Special Report: Understanding Canine Cancer
Written by Rhonda Hovan
Rhonda Hovan has been a breeder and owner-handler of Golden Retrievers
for more than thirty years. As a freelance writer, she has won both
the Veterinary Information Network Health Education Award and the
Eukanuba Canine Health Award. Rhonda is the Research Facilitator for
the Golden Retriever Club of America and founded the Starlight Fund at
the AKC Canine Health Foundation to support Golden Retriever health
research. She also serves on the Advisory Board of the National
Canine Cancer Foundation, and is an emeritus Director of the
Orthopedic Foundation for Animals. Rhonda can be reached at
RhondaHovan@aol.com
.
http://www.vetmed.ucdavis.edu/CCAH/documents/newsletter_2008_fall.pdf
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| Dog Disease Research at Broad Institute
Broad Institute Studies
http://www.broad.mit.edu/mammals/dog/donate.html
Mast Cell Tumors (MCT) Update
MCTs are cancerous proliferations of mast cells.
Although they can and will spread throughout the
body, the danger from MCTs comes from the secondary
damage caused by the release of chemicals the tumors
produce. These chemicals can cause systemic problems
that include gastric ulcers, internal bleeding, and
a range of allergic manifestations. We have compared
the genomes of 88 Golden retrievers with MCT and 103
healthy Golden retrievers and are very excited to
have identified several regions of the genome that
appear to be inherited risk factors for mast cell
tumors in Golden retrievers. We are now validating
these results in more dogs and looking to identify
the exact gene and mutation that will allow the
development of genetic tests and better treatments.
Hemangiosarcoma (HSA) Update
Hemangiosarcomas are rapidly growing and highly
invasive, blood-fed tumors. Blood vessels grow from
the tumor and often cause death through excessive
blood loss due to rupturing of the tumor. After
comparing the genomes of ~100 healthy dogs with ~100
dogs with HSA we were able to identify several areas
of the genome that were possible associated to
inherited HSA risk factors. Currently, five genes
found to be associated with the disease are being
searched for mutations. Once the mutations have been
identified and their presence in different breeds
assessed, this will allow for rapid development of
genetic tests for carriers of HSA.
We are also working with the European LUPA project,
a collaboration between 22 institutions in 11
countries, to map more than 20 traits including
cancers, inflammatory diseases, cardio-vascular
disease, neurological disease and other monogenic
traits. For more information please see
http://www.eurolupa.org/.
More information about some of our projects is
available at our website (www.dogdna.org).
If you have specific questions, please contact us at
dog-info@broad.mit.edu. Thank you again for all
of your help.
Best regards,
The Canine Genetics Group at the Broad Institute
|
|
SMILING BLUE SKIES ® IS FUNDING THE VERY FIRST
COMPANION ANIMAL CANCER REGISTRY IN NORTH AMERICA
Researchers at OVC are establishing
a population-based companion animal cancer registry.
The registry project will begin as a pilot project
focusing on all cancers within the dog and cat
population in the city of Guelph (but will be
expanded over time!). Cancer registries are an
integral part of human cancer research. However, for
companion animals, such registries do not exist in
North America. Population-based cancer registries
enable epidemiologists to study the occurrence of
cancer in the population and to make statements
when, where and why the occurrence of cancer is more
or less likely in the population. This is a huge
step forward and we could not do this without your
continued support. |
| ROUSE MEMORIAL FELLOWSHIP TO FUN COMPARATIVE CANCER RESEARCH
The Ontario Veterinary College, in conjunction with the Institute for
Comparative Cancer Investigation at the University of Guelph, is
pleased to announce the call for applications for the Arthur Rousse
Memorial Senior Fellowship in Veterinary and Comparative Cancer
Studies. This endowed fellowship provides $60,000 per year salary
support for up to 3 years, to a highly qualified individual interested
in pursuing aspects of veterinary and comparative cancer at the
postdoctoral level.
The 2008 competition is particularly directed towards individuals with
research training who wish to gain further experience in comparative
cancer research at a veterinary institution. In conjunction with the
Institute for Comparative Cancer Investigation, including the Animal
Cancer Centre in the Teaching Hospital of the Ontario Veterinary
College, the incumbent will partake in research to examine aspects of
companion animal cancer such as diagnostic procedures, therapeutic
approaches, and cancer pathobiology.
Qualified individuals who hold the DVM/DMV/VMD/ and have completed a
PhD/DVSc and/or an oncology or related residency (e.g., anatomic or
clinical pathology, pharmacology, surgery, internal medicine,
oncology, radiation oncology), with a strong interest in veterinary
research are encouraged to apply. Interested individuals should
provide a detailed statement of research interests and career goals,
Curriculum Vitae highlighting the details of clinical training and
research accomplishments, and the names and contact information of
three referees.
Applications should be sent to:
Office of the Dean, Ontario Veterinary College
Attention Dr. R. Jacobs
University of Guelph
Guelph ON Canada N1G 2W1
Application Deadline: March 28, 2008, with an expected start date of
September 2008
|
From the GRCA Health &
Genetics Committee
One of the research studies that GRCA and the Golden
Retriever Foundation support is in urgent need of
blood samples from any registered Golden Retriever
that has (at any time in its life) been definitely
diagnosed with a mast cell tumor. The diagnosis must
have been confirmed with a pathology report, and the
dog must not have had any other malignancy.
Confidentiality will be maintained. Owners can
contact Dr. Cheryl London at
London.20@osu.edu
(preferred) or via phone 614-292-9554.
Please feel free to contact the GRCA Research
Facilitator, Rhonda Hovan, with any questions at
London.20@osu.edu
or 330-668-0044. |
Notice from the GRCA Health & Genetics Committee
The Vector Borne Disease Diagnostic Laboratory at the NCSU
College of Veterinary
Medicine is recruiting cases for a funded research project,
which is investigating the potential role of selected flea-
and tick-borne bacteria as co-factors in the development of
lymphoma in Golden Retrievers. This two-year study is being
funded exclusively by the Golden Retriever Foundation and
the Canine Health Foundation.
The 1998 Golden Retriever Health Survey showed a
statistically significant decrease in lymphoma among Golden
Retrievers that had been treated with flea and tick
prevention products. This research project will examine one
mechanism by which these data might be explained - that
infection with Bartonella, Ehrlichia, and/or Anaplasma
species bacteria may predispose susceptible dogs to develop
lymphoma.
The purpose of this study is to search for evidence of
Bartonella, Ehrlichia, and/or Anaplasma infection in Golden
Retriever dogs with lymphoma, as compared to age- and
sex-matched Golden Retrievers from the same geographic
region. Obtaining identical samples from healthy control
dogs will be critical to the scientific evaluation of data
obtained from Golden Retrievers with lymphoma.
Click here to continue
reading this article, and download required documents
| To All Golden Owners:
Cancer Sample Donation Chart
Please download the PDF document
containing:
Contact
Information for Participation in Golden
Retriever Cancer Research
Click here to open or download |
URGENT
Blood samples
are needed from registered
Golden Retrievers diagnosed with a mast cell tumor.
| To All Golden Owners:
There has been some discussion and confusion in recent days regarding
recruitment of Goldens with hemangiosarcoma (and other cancers) to
donate blood and tissue samples for use in research, because owners
understandably want to be certain that these samples go to studies
that will benefit the breed. GRCA and the Golden Retriever
Foundation (GRF) have developed procedures to help ensure that the
scientific studies they support are held to the highest research
standards, and have the greatest likelihood of producing results that
will benefit dogs. These procedures begin with two levels of
scientific review at the Canine Health Foundation, followed by review
and recommendations from the GRCA Health & Genetics Committee (H&G),
and final review and funding decisions by the GRF. Once a project is
funded and underway, it is required to submit regular progress and
financial reports, which are reviewed by the Science Officer at CHF,
and by the H&G. These procedures have contributed to the excellent
track record of GRCA and GRF supported research producing results
that meet standards for publication in peer-reviewed scientific
journals; and indeed, some of this research is already benefiting
Goldens at the clinical level.
GRCA and GRF have recruitment notices for many of these studies
posted on their web sites, and every issue of the GRNews includes
contact information for the Research Facilitator for assistance and
referral to studies for which individual dogs may qualify. However,
perhaps by the very nature of worried owners of affected dogs who may
be looking for the latest and newest hope, it appears that these
notices may get overlooked in favor of "new bulletins" that can be
rapidly circulated on the Internet. This is understandable, but
sometimes can lead to confusion and perhaps inadvertent misdirection
of valuable blood, tissue, or DNA samples. In the most recent
example, it is our understanding that the research mentioned is
actually the same research for which GRCA and GRF notices have been
recruiting for some time, and already had collection procedures in
place. Adding an intermediary third party to the process has the
potential to separate owners from the scientists doing the research,
and to inadvertently introduce errors or omissions in the information
transfer.
We encourage owners to participate in research whenever possible, and
we suggest that the most efficient sample collection process is the
one supported by GRCA and GRF, in which the samples go directly to
the scientists involved in the research. At the present time, all
blood (and sometimes tumor samples) from Goldens with any form of
cancer can be sent to one researcher, Jaime Modiano, VMD, PhD, who by
agreement then distributes the DNA to several different studies as
needed. These studies include, but are not limited to, those headed
by Dr Kerstin Lindblad-Toh, Dr Matthew Breen, Dr Elaine Ostrander,
and Dr Stuart Helfand. Information regarding sample submission can
be obtained from Dr Modiano's website http://www.modianolab.org/
index.shtml or by contacting the Research Facilitator at
rhondahovan@aol.com.
In addition, blood samples only (not tissue) from both normal Goldens
and those with cancer, may be sent to Dr Lindblad-Toh, with further
information available at http://www.broad.mit.edu/mammals/dog/pdfs/
dog_project_info.pdf A complete listing of research recruitment
needs for studies funded through the Canine Health Foundation is
available online at
http://www.akcchf.org/research/participation.cfm
We hope that this will serve to clarify some of the questions we have
received in recent days, and we also intend to work on additional
procedures which will make it easier for owners to assist research
that benefits the breed. With the numerous research studies
currently ongoing, and many more in the planning stages, there are
excellent choices for owners who wish to donate samples - and best of
all, that means there is a whole lot of hope to go around!
Sincerely,
The Golden Retrieveer Club of America Board of Directors
The Golden Retriever Club of America Health & Genetics Committee
The Golden Retriever Foundation |
The 4th Genes Dogs and Cancer Conference, was held
on
September 14th to the 17th, 2006 at the
Crowne Plaza Chicago Metro, in
Chicago Illinois.
Conference Coordinators
Timothy Fan, Kevin Hahn, Chand Khanna, Jaime F.
Modiano, and Elaine Ostrander
Sponsored by Jeffrey Pepper, the French Bulldog Club
of America, Morris Animal Foundation,
the National Beagle Club, the Orthopedic Foundation
for Animals, the Soft Coated Wheaten
Terrier Club of America Endowment Fund and the
Starlight Fund
This conference brought together researchers,
veterinarians and breeders from around the
world to discuss advances in canine cancer research.
Join us to hear presentations on the
following four topics:
Host and Microenvironment: Genetics and Host
Interactions
Cancer Pathogenesis and Progression: Metastasis,
Angiogenesis and Cytogenetics
Discovery and Delivery: Cancer Care, Diagnostics,
Imaging, Therapy and Monitoring
Program Updates: Clinical Trials, Consortia,
Regulatory Agencies
Keynote speaker Dr. Janet Rowley and Distinguished
Speakers Drs. Elaine Ostrander, Tom
Rosol and Chand Khanna presented their research
on topics such as the molecular origins of
cancer, inherited cancers, metastasis and
comparative oncology translation and biology.
DOGS ARE KEY TO REVOLUTIONARY CANCER STUDY
CANINE CANCER PATIENTS HELP ADVANCE RESEARCH ON
PROMISING VACCINE
JOHN BERMAN
Dec. 3, 2007—
Kyra looks like any other energetic Rhodesian
Ridgeback dog, but she's also a cancer survivor --
and a reason for hope.
Two years ago, the 10-year-old canine's owner,
Eileen Eisenhower, noticed an eerily familiar lump
on Kyra's leg. Eileen is a nurse who treats human
cancer patients.
"I said, 'Oh, Kyra, you have lymphoma," Eisenhower
recalled lamenting. "I just knew it."
But Eisenhower converted her pain into promise,
enrolling Kyra in a revolutionary vaccine study at
the University of Pennsylvania, which had an
unlikely collaboration between canine veterinarians
and human oncologists.
Four million dogs are diagnosed with cancer every
year -- cancers very similar to the human versions.
"Down to the microscope, they look very similar and
they behave similarly," Dr. Robert Vonderheide at
the Abramson Cancer Center at the University of
Pennsylvania said.
And this translates into the most promising aspect
of this study: "They also respond to treatment very
similarly," Vonderheide points out.
One of the greatest advantages to studying dogs is
they age faster -- literally, in "dog years," so
scientists can get the results of their studies more
quickly.
"It's like a compressed biological life span that we
can study -- the cancer progression -- and also
potentially the response to therapy," said Dr. Karin
Sorenmo, associate professor of oncology at the
University of Pennsylvania School of Veterinary
Medicine.
In the study involving Kyra, doctors took genetic
material from a cancerous tumor, implanted it in
healthy infection-fighting b-cells outside the body
to train them to attack the lymphoma, and then
injected it back into Kyra.
Sorenmo was encouraged by the results. "I'm hoping
that this is just the beginning of more trials that
can benefit helping dogs, helping people."
Kyra is back to her hyperenergetic and healthy self.
She and a number of the dogs in the study are now
cancer-free. The researchers estimate they are
within two years of testing the vaccine on humans.
Without the dogs, they would be more than a decade
away.
"If we didn't have this information that we're
learning from vaccinating people's pets, we would
still be studying the vaccine in laboratory dishes
without a real hope of going forward in the near
future," Vondreheide said.
The researchers' optimism resonates on multiple
levels for Eisenhower, as a grateful dog owner and
dedicated cancer nurse.
"I hope that someday I can give this vaccine to
people and to kids -- and to, you know, let people
know how it started and where it came from,"
Eisenhower said.
She can tell them it came from man's best friend.
Copyright © 2008 ABC News Internet Ventures
* * * * * * * * * * * * * * * * * * * *
CONTACT INFORMATION
Dr. Robert Vonderheide, MD, D. Phil.
Assistant Professor of Medicine in the Cancer
Biology Programme and the Gene Therapy and Vaccines
Programme
University of Pensylvania School of Medicine
His office telephone number is 215-573-4265 and his
email addres is rhv@mail.med.upenn.edu
Dr. Vonderheide graduated from the University of
Notre Dame with a B.Sc. in Chemical Engineering in
1985 and from Oxford University, England , as a
Rhodes Scholar with a D.Phil. in immunology in 1989.
After graduating from Harvard Medical School in
1993, he completed a residency in Internal Medicine
at the Massachusetts General Hospital and
subsequently a clinical fellowship in hematology-oncology
at the Dana-Farber Cancer Institute. He joined the
University of Pennsylvania in 2001 as assistant
professor in medicine and an investigator at the
Abramson Family Cancer Research Institute. He is
funded by the NIH, the Beckman Foundation, the
Leukemia and Lymphoma Society, and the Alliance for
Cancer Gene Therapy.
Research Area: Infectious Disease
Breed: Golden Retriever
The Vector Borne Disease Diagnostic Laboratory at
the NCSU College of Veterinary Medicine is
recruiting cases for a funded research project,
which is investigating the potential role of
selected flea- and tick-borne bacteria as co-factors
in the development of lymphoma in Golden Retrievers.
The 1998 Golden Retriever Health Survey showed a
statistically significant decrease in lymphoma among
Golden Retrievers that had been treated with flea
and tick prevention products. This research project
will examine one mechanism by which these data might
be explained - that infection with Bartonella,
Ehrlichia, and/or Anaplasma species bacteria may
predispose susceptible dogs to develop lymphoma.
The purpose of this study is to search for evidence
of Bartonella, Ehrlichia, and/or Anaplasma infection
in Golden Retriever dogs with lymphoma, as compared
to age- and sex-matched Golden Retrievers from the
same geographic region. Obtaining identical samples
from healthy control dogs will be critical to the
scientific evaluation of data
obtained from Golden Retrievers with lymphoma. Dr.
Ed Breitschwerdt
is the principal investigator and Ashlee Duncan is
the graduate
student responsible for the project. The entry
criteria for a case
include: Golden Retrievers with a new diagnosis of
lymphoma that have not received any antibiotics
within 14 days prior to sample collection (or 30
days for azithromycin). Samples should be collected
prior to induction of chemotherapeutic agents.
The minimum entry criteria for a control include:
Golden Retrievers residing within 100 miles of the
case dog and lacking clinical evidence of
lymphadenopathy, making the possibility of
undetected lymphoma unlikely. Additionally, these
control dogs must not have received any antibiotics
within 14 days prior to sample collection (or 30
days for azithromycin). For each case, two to three
control dogs will be utilized. If possible, these
healthy dogs should be similar in age (± 18 months)
and sex as the case dog. Healthy dogs may be
identified by the owner of the case dog, selected by
the case's attending veterinarian, or recruited
through the Golden
Retriever Club of America. Cases and controls
recruited will
receive free serological and molecular testing for
Bartonella, Ehrlichia, and Anaplasma (a $360.00
value based on current serology/ PCR testing costs
in our laboratory). Samples to be collected for this
research include whole blood, serum, lymph node
aspirate(s), and buccal swab(s).
Please contact us at 919-513-8279 or
awduncan@ncsu.edu for further information.
Research Area: Canine Cancer
Breeds: Akita, American Cocker Spaniel, Boxer,
Bullmastiff, Chinese Shar-Pei, Chow Chow, English
Cocker Spaniel, English Springer Spaniel,
Flat-Coated Retriever, German Shepherd, Giant
Schnauzer, Golden Retriever, Greyhound, Labrador
Retriever, Leonberger, Mastiff, Miniature Poodle,
Miniature Schnauzer, Pointer, Pug, Rottweiler,
Scottish Terrier, Standard Poodle, Standard
Schnauzer, Toy Poodle
After completing the dog genome sequencing
project, the Broad Institute of Harvard and MIT and
collaborators are now working on identifying disease
genes predisposing to cancer. Identification of such
genes could lead to carrier testing, a better
understanding of the disease and long term better
treatments for the disease in both dogs and humans.
More information can be found at:
www.broad.mit.edu/mammals/dog
http://www.broad.mit.edu/mammals/dog.
For each of the below diseases researchers need
blood samples from affected dogs as well as blood
samples from healthy older (>6 yo) dogs.
Mammary tumors
PI: Kerstin Lindblad-Toh Broad and Elizabeth
McNiel, U. Minnesota
Focus: English Springer Spaniel
Additional breeds included: German Shepherds, Cocker
Spaniels and Boxers
Please contact:
Dog-info@broad.mit.edu
Melanoma
PI: Kerstin Lindblad-Toh Broad and Phil Bergman,
Animal Medical Center, NY Breeds included: ALL
including Scottish Terriers, Cocker Spaniels, Black
Labrador Retrievers, Rottweilers, Chow Chows, and
Pugs
Please contact:
Dog-info@broad.mit.edu
Lymphoma
PI: Kerstin Lindblad-Toh, Broad
Focus: Golden Retrievers, Boxers
Additional breeds included: Cocker Spaniel,
Rottweiler, Akita, Flat- Coated Retriever
Please contact:
Dog-info@broad.mit.edu
Mast cell tumors
Collaborators: Kerstin Lindblad-Toh, Broad and
Cheryl London, UC Davis
Focus: Pugs and Chinese Shar-Pei
Additional breeds included: Pit Bull Terrier,
Labrador Retriever, Golden Retriever, German
Shepherd, Cocker Spaniel, Boxer
Please contact:
Dog-info@broad.mit.edu
Researchers at the AMC Cancer Research Center and
University of Colorado Health Science Center are
looking for samples for the following projects:
Lymphoma
Researchers need samples from any dog that has an
AKC registration number.
Eligible dogs will undergo standard of care
treatment and provide blood samples as well.
Availability of 2 or more unaffected relatives that
are >6 years old is desirable. They also would
encourage people who have dogs that are related to
study subjects that are affected to participate.
Owners of all dogs will be asked to fill out a
follow-up questionnaire.
Hemangiosarcoma
Researchers need blood samples from affected dogs
for a study to map susceptibility genes. In some
cases, samples may be applied to the development of
a diagnostic test for hemangiosarcoma. Eligible dogs
must have an AKC registration number. Owners of all
dogs will be asked to fill out a follow-up
questionnaire.
Visit
www.modianolab.org
http://www.modianolab.org
for additional information on these programs.
Thank you for your attention.
|
INNOVATIVE SCREENING & TREATMENT PROGRAMME AVAILABLE FOR CANINE
LYMPHOMA CANCER
Recently, I received a note from Graeme Radcliffe, one of the key "movers and
shakers" behind PetScreen/Tri-Screen.
Graeme told me that they had been involved in research and development for the
past two years, and the end result was a special announcement made at the
Veterinary Cancer Society Annual Conference in November, 2011.
The Tri-Screen test is available in a diagnostic kit format and will tell a
veterinarian/owner immediately, if a canine patient has lymphoma, or another
medical issue that can be treated without invasive surgery. The Veterinary Caner
Society delegates were very supportive of the presentation.
Graeme is hoping that when the Morris Animal Foundation begins their giant
longitudinal study for Golden Retrievers, that they will be involved.
Graeme and I are keeping in close touch with each other, and has provided me
with a PDF about the use of CART algorithms to combine serum acute phase protein
levels as a diagnostic aid in canine lymphoma.
This information will be posted on the Smiling Blue Skies website, but if you
would like a copy of the PDF, simply send me an email, and I will send it along
to you.
You can also check out
http://www.tri-screen.net/
In the mean time, here is the Press Release:
Albuquerque, NM … November 2011 --- A new diagnostic kit which takes the
uncertainty out of lymphoma diagnosis, has been launched at the Veterinary
Cancer Society’s annual conference this month.
Developed by PetScreen (www.pet-screen.com)
in the UK, the announcement is a significant breakthrough in the diagnosis of
canine lymphoma with the major benefit being that it is able to differentiate
between patients with lymphadenopathy due to lymphoma and lymphadenopathy due to
other ailments such as lymphoid hyperplasia.
The announcement also signals a partnership and commercial venture between
PetScreen Ltd and Tridelta Development Ltd to jointly develop manufacture and
market a unique range of veterinary cancer diagnostic kits under the banner of
‘Tri-Screen’ (www.tri-screen.net).
PetScreen has established the first reference laboratory offering the Advanced
Lymphoma Blood Test (ALBT) utilising the Tri-Screen Canine Lymphoma assay kit.
The kit is available now to enable laboratories worldwide to offer veterinarians
this advanced testing system.
For the past two years, PetScreen’s research team have been busy characterising
and identifying the biomarkers used in their earlier lymphoma blood test. They
found that two of the markers are Acute Phase Proteins (APP’s). Although APP’s
have been investigated in veterinary medicine for some time PetScreen has
developed a unique multi-marker approach which led to the development of
patented and copyrighted analytical algorithms which combine the relative values
of both Haptoglobin and C-Reactive Protein (CRP) in serum.
By enlisting the support of vets in the UK and USA the assay has been rigorously
tested with 194 canine patients with lymphoma, benign lymphoid hyperplasia and
other diseases with similar presentation to lymphoma as well as healthy dogs.
By testing the acute phase proteins using immunoassay, PetScreen achieved
excellent levels of high performance, reproducibility and objectivity. The
combination of the three diagnostic elements enables differentiation with a very
high degree of sensitivity and specificity … ensuring an appropriate treatment
regimen can begin at a critical early stage of disease identification and
development.
In order to make this available to a global reference laboratory market, a
partner with a unique understanding of APP diagnostic kit manufacture and
marketing was required … it quickly became apparent that Tridelta’s reputation
and experience with the international pharmaceutical industry in this niche
sector qualified their preferred partner status. Each company briogs its own
strengths to the Tri-Screen brand of diagnostic kits. For Tridelta it is
an!important step into the companion animal marketplace; for PeuScreen, the
opportunity to globalise and advance their veterinary diagnostics expertise in
tiis important and rapidly emerging sector.
.
www.pet-screen.com:
PetScreen: Detecting and Treating Cancer BioCity Pennyfoot Street
Nottingham NG1 1GF United Kingdom

Professor Graeme Radcliffe
Chairman PetScreen Limited
BioCity Nottingham
Pennyfoot Street
Nottingham
NG1 1GF
UK
graeme.radcliffe@btconnect.com
www.pet-screen.com
tel: 08000 284 811 (Free - UK Only)
fax: 0115 912 4431
mobile: +44 (0)115 912 4430
+44 (0)115 912 4431
07785 238427
|
Auburn to Study Treatment for Lymphoma in Dogs
http://www.avma.org/onlnews/javma/dec06/061201i.asp
Auburn University has received $1.4 million from the
National Cancer Institute at the National Institutes
of Health to study a new therapy for lymphoma in
dogs.
Researchers plan to modify a nonreplicating virus,
administer the virus to dogs with lymphoma, and
administer a drug to the dogs. The virus will infect
lymphoma cells and then encode a protein to convert
the drug into a toxin to kill the cells.
Lymphoma is the third most common cancer in dogs.
Average life expectancy for dogs undergoing
chemotherapy is about one year.
Without any treatment, life expectancy is about two
months from the time of diagnosis.
The grant from the National Cancer Institute covers
two years of laboratory work and three years of
clinical trials.
Dr. Bruce Smith, with the College of Veterinary
Medicine's Scott- Ritchey Research Center, is
leading the study. Auburn co- investigators include
Drs. Curtis Bird, Mary Lynn Higginbotham, Annette
Smith, and Elizabeth Whitley.
The
Golden Retriever Club of America is pleased to
announce that Golden Retrievers will be one of the
pilot breeds currently eligible for participation in
a new DNA database. The mapping of the canine genome
is expected to have a significant impact on research
activities regarding canine genetic disease, and
thus there is growing interest among breed clubs and
breeders to establish a DNA bank to facilitate
research and future disease testing on individual
dogs. In response to this evolving need, CHIC
(Canine Health Information Center) and OFA have
established a DNA bank and database designed to
serve both breeders and researchers.
This DNA
database will serve the canine research community by
providing researchers with optimized family groups
needed for specific research studies, and will
facilitate more rapid progress in research by
expediting the sample collection process. It will
also allow breeders to take advantage of future
DNA-based disease tests as they become available,
with the ability to test both current breeding dogs,
and important dogs of the past whose DNA is stored
in the bank. Researchers funded by such
organizations as the Canine Health Foundation and
Morris Animal Foundation can apply to use this DNA
for specific studies; and owners will have access to
their dog's DNA for DNA-based disease testing.
DNA
databases are most useful when the DNA is linked to
both a health history (including but not limited to
phenotypic health "clearances"), and to a pedigree.
This provides researchers with the ability to select
the samples that are of interest to particular
studies, by searching the database for dogs that
meet specific eligibility criteria. However, all
individual dogs, pedigrees, and owners will be coded
for anonymity, which can be waived only by the
owner. Privacy will be carefully protected according
to the instructions of the owner. The owner will
also be provided with an individual access code
which will permit him or her to update the health
history over the lifetime of the dog, since many
health conditions of interest may not have developed
at the time the dog was entered into the database.
DNA can be
collected through either a blood sample, or by using
buccal (cheek) swabs. Blood samples provide an
almost unlimited supply of DNA, while buccal swabs
provide adequate DNA for a number of health studies
and testing, although significantly less than blood
samples.
Double the
Benefit!
In addition to
collecting blood samples at the National for future
research to be stored in the DNA bank, a current
study supported by the Golden Retriever Foundation
and GRCA will also be collecting blood samples at
the National Specialty. This important research is
being conducted at the Broad Institute of the
Massachusetts Institute of Technology, and is
attempting to identify genes involved in
osteosarcoma and other cancers in Goldens. In a
cooperative effort to double the usefulness of each
sample, dogs may contribute to both programs with
only one blood sample, which will be shared (with
the owner's permission) between the DNA bank and the
Broad Institute's canine genomic research team.
As part of
GRCA's participation as a pilot breed, CHIC/OFA will
send a representative to the 2005 National Specialty
to assist with enrolling as many Goldens as possible
into the database. There will be volunteers on site
to draw blood or assist with buccal swab
collections, and computer capability to process the
dog into the database. There will be no charge to
enroll a dog in the DNA database at the National
Specialty! In addition, for the first 12 months,
there will be no charge to enroll dogs using buccal
swabs providing the dog has a CHIC certificate (see
http://www.caninehealthinfo.org/ )
Your
participation in this important database will assist
health research for decades to come, and we urge
everyone to enroll as many dogs as possible in both
of these programs. Please come to the collection
center on the grounds of the National Specialty on
Wednesday or Thursday, September 28 or 29, and show
your support for a healthier future for Golden
Retrievers. Owners not attending the National are
also strongly encouraged to participate in the DNA
bank, with enrollment information available on the
GRCA website at
www.grca.org (link coming soon) or by writing to
edziuk@offa.org Costs are $10 using buccal swabs
(free for CHIC dogs until Sept, 2006), and $25 using
blood samples.
Please Spread
the Word!
Patient Disease: Canine
Patients with Soft Tissue Sarcoma
Study Name: Canine Soft Tissue Sarcoma Vaccine Study
Purpose of the Study: The purpose of this study is
to evaluate the effectiveness, and to establish the most
appropriate dose of a vaccine intended to inhibit the growth
of new blood vessels in tumours. The vaccine is prepared
using the DNA from human blood vessel growth factors. Using
this specially prepared vaccine, we hope to stimulate a
canine patient's immune system to make antibodies against
newly forming blood vessels in a tumour.
Patient Entry Criteria: In general, these studies
are available to qualifying patients living within 100 miles
of the Animal Cancer Centre at Colorado State University.
The patient must have the disease of soft tissue
sarcoma, which has been confirmed by biopsy. The soft
tissue sarcoma must be measurable and accessible to
biopsy. The disease may not have spread to any other area
of the body. In order to qualify for this study, treatment
prior to presentation to the Animal Cancer Centre must
have been very limited. The patient is not to have received
radiation therapy, any chemotherapy, or any holistic medical
treatment for soft tissue sarcoma prior to entry into the
study. The patient must not have received steroids or NSAIDs
for four weeks before presentation. No other medical
conditions may be present that might limit the patient's
life. No additional medication may be given once the
patient is enrolled in the study. For more information
regarding entry criteria, please contact the
Consult Coordinator at 970-297-4195.
Owner Responsibilities: After the initial diagnostic
visit, the client is required to bring the patient
to regularly scheduled visits for treatment and evaluation
for up to a year. The client must allow a total of three
biopsies to be taken (one pre-treatment and two during
treatment) to assess the patient's response to the vaccine.
These biopsy procedures require the patient to be profoundly
sedated or anesthetized. No additional medication may be
given once the patient is enrolled in the study.
Procedures or treatments unrelated to the study will be the
owner's financial responsibility.
Financial Incentives: The owner pays for the initial
diagnostic work up, usually $300 to $400. The study pays
for all treatment procedures and for all evaluation recheck
visits for a period of one year. For more information
regarding financial incentives, please contact the Consult
Coordinator at
970-297-4195.
Patient
Disease: Canine Hemangiosarcoma of the Spleen
Study Name: Hemangiosarcoma Metronomic Chemotherapy
Study
Purpose of the Study: The purpose of this study
is to evaluate the effectiveness of metronomic
chemotherapy for the treatment of canine splenic hemangiosarcoma.
Metronomic chemotherapy is a method of delivering
chemotherapeutic agents at lower doses, but
administering the doses more often. This study is
designed as a randomized clinical trial. There are two
treatment groups. One group receives doxorubicin (Adriamycin)
chemotherapy every two weeks for five treatments.
The other group receives metronomic chemotherapy using
etoposide, cyclophosphamide, and piroxicam.
Patient Entry Criteria: In general, these
studies are available to qualifying patients
living within 100 miles of the Animal Cancer Centre at
Colorado State University. The patient must have the
disease of hemangiosarcoma of the spleen, which has been
confirmed by biopsy and histopathology. The spleen must
be surgically removed and the disease may not
have spread to any other area of the body. In order to
qualify for this study, the patient is not to have
received radiation therapy, any chemotherapy, or any
holistic medical treatment for splenic hemangiosarcoma
prior to entry into the study. The patient must not
have received steroids, like prednisone, for three weeks
prior to presentation. No other medical conditions may
be present that might prevent the patient
from completing the study. No additional medication
related to the disease may be given once the patient is
enrolled in the study. For more information regarding
entry criteria, please contact the Consult Coordinator
at 970-297-4195.
Owner Responsibilities: This study requires
frequents visits to the Animal Cancer
Centre. The client must schedule and keep all
appointments related to the study. Should the owner
decide to withdraw from the study, the owner assumes
responsibility for all costs incurred.
Financial Incentives: The owner pays for the
initial diagnosis and surgical treatment of
the disease. Additionally, the owner is responsible for
the cost of the staging tests used to determine if the
patient meets the eligibility requirements of the study
(usually about $600). Once eligible, the study pays for
all study-related examinations, tests, and
chemotherapy treatments for up to one year. For more
information regarding financial incentives, please
contact the Consult Coordinator at 970-297-4195.
Patient Disease: Canine Osteosarcoma of a Limb
Study Name: Osteosarcoma and Meloxicam Study
Purpose of the Study: The purpose of this study
is to evaluate the benefits of the drug meloxicam in the
postoperative pain management of canine patients with
osteosarcoma.
Patient Entry Criteria: In general, these
studies are available to qualifying patients
living within 100 miles of the Animal Cancer Centre at
Colorado State University. Eligible patients are dogs
with histologically confirmed osteosarcoma of an
extremity. The patient's treatment plan must include
amputation of the effected limb followed by
doxorubicin (Adriamycin) chemotherapy. Diagnostic
evaluation must indicate no spread of cancer in the
patient. Additionally, the patient must have
no pre-existing heart condition that would make
doxorubicin an inappropriate choice for treatment.
Patients may not have concurrent disease that might
prevent them from completing the study.
Owner Responsibilities: This study pays only the
cost of meloxicam. The client is responsible for all
costs related to the diagnosis and treatment of the
patient's cancer, and for all costs related to
complications that might arise as a result of treatment
of the patient's cancer.
Financial Incentives: This study pays only the
cost of meloxicam. For more information regarding
financial incentives, please contact the Consult
Coordinator at 970-297-4195.
Patient
Disease: Canine Patients with Biopsy Confirmed Cancer
Study Name: Silibinin for Canine Tumours
Purpose of the Study: Silibinin is the active
ingredient in the herbal compound milk thistle. In
mouse and human tumour cells, silibinin has been shown
to inhibit the growth of many types of tumours. In this
study we will determine the maximum dose of silibinin
that can be safely given to tumour bearing dogs. We
will also investigate how effective this compound is in
the canine patient.
Patient Entry Criteria: In general, these
studies are available to qualifying patients
living within 100 miles of the Animal Cancer Centre at
Colorado Sate University. The patient will be screened
by a variety of diagnostic tests as well as undergo a
small biopsy procedure. The owner is
financially responsible for tests to meet entry
criteria. The patient entry criteria
are as follows:
1. Dogs with a histologically confirmed malignant
tumour that is in a location that is easily biopsied.
2. Conventional therapy must have been declined by the
owner, or must have failed.
3. Dogs must be free of other life threatening disease.
4. Dogs may not have received chemotherapy within two
weeks prior to study entry.
5. Dogs may not have received radiation therapy within
six weeks prior to study entry.
6. Other medications are generally acceptable as long
as they were begun before entry into the study.
7. Dogs must have relatively normal blood work
Owner Responsibilities: Owners are responsible
for delivering the study medication (a powder that can
be mixed in a small amount of food) three times
daily. Owners are required to make and keep all
appointments. Following the initial visit, the patient
will be required to return after one week and
then again two weeks later. The owner is financially
responsible for the initial tests to see if the patient
qualifies for the study, and any costs that follow the 3
week recheck.
Financial Incentives: The study will pay for the
blood tests and biopsy at the beginning of the study,
and the one week and three week recheck appointments.
The drug costs will be covered during the three week
study period. After this time, if a patients disease is
stable or improved, the drug will continue to be
available at no cost; however, a small distribution fee
will be assessed by the Pharmacy.
Patient Disease: Canine Mast Cell Tumour Disease
Study Name: Novel Drug Trial for Mast Cell Tumors
Purpose of the Study: The purpose of this study
is to demonstrate the effectiveness and safety of a
novel drug to control grade II and III mast cell tumours
in the canine patient.
Patient Entry Criteria: In general, these
studies are available to qualifying patients
living within 100 miles of the Animal Cancer Centre at
Colorado State University. The patient entry criteria
are as follows:
1. Canine patients with one or several mast cell
tumours (grade II or III) that have returned after
surgery or have been described as non-resectable.
2. Dogs must be older than six months of age and weigh
more than 7 pounds.
3. If patients have received chemotherapy, steroids, or
had surgery, the study will be delayed by 2 weeks.
4. Dogs that have received radiation therapy must wait
6 weeks before beginning the study.
5. The patient may not have spread of the disease to
the lymph nodes or other site.
6. Blood work must be relatively normal.
7. Dogs must be free of other life threatening disease.
Owner Responsibilities: The owner is responsible
for the initial examination fee. The owner must
schedule and keep all appointments as dictated by the
study. The owner must administer the study medication
on a daily basis, and must keep a treatment diary, for
up to six months.
Financial Incentives: The patient will be
screened by a variety of diagnostic tests and
may undergo a small biopsy procedure. A portion of the
cost of these tests will be paid for by the study. Upon
entry into the study, the study pays for subsequent
screening visits and diagnostic tests as well as all of
the treatment visits.
Patient Disease: Canine patients with a Biopsy
Confirmed Malignant Tumour
Study Name: Canine PEG -TNF Study
Purpose of the Study: PEG-TNF is a new
formulation of a naturally occurring human hormone. In
this study we will determine the maximum dose of PEG -TNF
that can be safely given to tumour bearing dogs. We
will also investigate how effective this compound is on
tumours, that is, their size, the blood flow within
tumours and on the tumour cells themselves.
Patient Entry Criteria: In general, these
studies are available to qualifying patients
living within 100 miles of the Animal Cancer Centre at
Colorado State University. The patient will be screened
by a variety of diagnostic tests and may undergo a small
biopsy procedure. The owner is financially
responsible for tests to meet entry criteria. The
patient entry criteria are as follows:
1. Dogs with a histologically confirmed malignant
tumour that is in a location that is easily biopsied.
2. Dogs must be free of other life threatening disease.
3. Dogs must have relatively normal blood work.
4. Patients may not have received steroids or NSAIDs
(aspirin-like drugs) for 72 hours prior to entry.
5. Dogs may not have received chemotherapy within two
weeks prior to study entry.
6. Dogs may not have received radiation therapy within
6 weeks prior to study entry.
7. Candidates must weigh at least 25 pounds.
8. Owners must agree to a postmortem examination
(autopsy) at the time of the pet's death or euthanasia.
Owner Responsibilities: Owners are financially
responsible for the diagnostic tests that determine if
the patient qualifies for the study. Owners are
required to make and keep all appointments.
Following the initial visit, the patient will be
required to return 4, 7, and 21 days after
treatment. Owners must comply with the study protocol.
It will be necessary for the patient to submit to having
blood samples drawn, the tumour biopsied, and
hospitalization. A Magnetic Resonance Image (MRI) may
be requested in certain cases. The patient must be
anesthetized for a MRI.
Financial Incentives: Once the patient has
satisfied the eligibility requirements for the
study, all costs associated with the study will be
paid. Additionally, a $250.00 VTH credit will be applied
toward any future treatments.
__________________________________________________________
 
Jaime F. Modiano, V.M.D., PH. D.
Scientist, Centre for Cancer Causation and
Prevention
AMC Cancer Research Centre
Associate Professor, Department of Immunology
University of Colorado Health Sciences Centre
303-239-3408
modianoj@amc.org
Dr. Modiano's lab, is interested in
understanding basic differences between
normal cells and tumour cells. Their
ultimate goal is to reduce the morbidity and
mortality associated with cancer in humans
and animals.? As they learn more about how
cancer cells differ from normal cells, they
can exploit these differences to improve
diagnosis and treatment and devise better
methods of prevention. The
purpose of their website, is to provide
information for individuals seeking to learn
more about cancer, to facilitate recruitment
into ongoing studies, and to foster
communication among scientists interested in
Cancer Biology, Immunology, and
Immunotherapy. Vistoris to their website,
will find links to publications, study
information and recruitment materials,
methods and reagents, collaborators, and
other useful sites that have cancer
information.
Suggestions and feedback are welcome at
info@modianolab.org__________________________________________________________

Oral Antimitotic Agent for Dogs with Lymphoma
|
Animal Cancer
Institute
Studies
Since its inception the Animal Cancer Institute
and its Network of veterinary oncologists have
offered cutting edge treatment options. The
Animal Cancer Institute Network is based in
Washington, DC and extends across the United
States with sites in California, Connecticut,
Florida, Maryland, Massachusetts, New Jersey,
New York, Ohio, Texas, Virginia and Washington .
It is the goal of the Animal Cancer Institute to
provide more effective and less toxic options
for the treatment of cancer. Collaboration with
the pharmaceutical industry allows these options
to be provided, in many cases, at substantially
reduced costs. For more information on the
therapeutic diet clinical study for cats with
lymphoma, and the Animal Cancer Institute, visit
our website at:www.animalcancerinstitute.com.
|
The Animal Cancer Institute, LLC
Cutting edge options for cancer
C. Khanna DVM, PhD, DACVIM
T. Rusk DVM
For more information, contact
Jennifer Turner:
Phone: 202-363-7300
Fax: 202-363-7126
Email:jturner@animalcancerinstitute.com
|
| |
|
You may register your clinic to receive
electronic updates on trials available to your
clients. Registration for eTrial Updates is
available at our website, www.animalcancerinstitute.com.
|
|
Oral Antimitotic Agent for Dogs with Lymphoma
|
|
Eligibility Criteria Include: |
-
measurable, cytologically diagnosed NH lymphoma
(histology collected at study entry)
-
any clinical stage but must have nodal
involvement- includes relapsed cases
-
favorable performance score
-
no concurrent chemotherapy (within 14 days of
trial entry)
-
no concurrent radiation therapy (within 21 days
of trial entry)
-
concurrent use of corticosteroids accepted
providing treatment duration is greater than 21
days and/or no clinical improvement is noted.
Measurable disease defined by examination,
radiographs, ultra-sound, CT or MRI scan
Trial Design:
Diagnostic and staging tests may be performed at any
veterinary hospital within 10 days of initiation of
study:
-
Serum biochemistry
-
CBC
-
Urinalysis
-
Thoracic and abdominal radiographs
Patients will be treated at a participating Animal
Cancer Institute Network clinic. Lymph node biopsies
will be required at entry, Day 7, first objective
response and at progression or relapse.
Trial Support/Funding Includes:
-
Laboratory, biopsy and professional fees (as
required for the study) from time of enrollment
through Day 56 (additional monthly exams beyond
Day 56 will be owner?s financial responsibility)
-
Oral Antimitotic agent through Day 56 (beyond
Day 56, additional monthly shipments of study
drug supply will be billed to the
clinic/investigator at a rate of $50 per
shipment)
Dogs will receive the oral medication over a 4-week
initial phase. Continued therapy will be available
pending response to therapy. Long-term follow-up
recheck examinations will be performed monthly. |
__________________________________________________________

Antiangiogenic Therapy for Dogs with Measurable
Soft Tissue Sarcomas
|
|
Animal Cancer Institute Studies
Since its inception the Animal Cancer Institute
and its Network of veterinary oncologists have
offered cutting edge treatment options. The
Animal Cancer Institute Network is based in
Washington, DC and extends across the United
States with sites in California, Connecticut,
Florida, Maryland, Massachusetts, New Jersey,
New York, Ohio, Texas, Virginia and Washington .
|
The Animal Cancer Institute, LLC
Cutting edge options for cancer
C. Khanna DVM, PhD, DACVIM
T. Rusk DVM
Study Monitor? Kate Cadorette
Phone: 202-363-7300 Fax: 202-363-7126
Email:kcadorette@animalcancerinstitute.com
|
|
Trial eligibility criteria include:
-
client owned pet dogs
-
measurable, histologically confirmed soft tissue
sarcomas, not including hemangiosarcomas
-
tumors must be accessible for histopath
collection and objective measurement using
direct caliper measurement, ultrasound,
radiographs or CT/MRI scan.
-
favorable clinical performance status at entry
(expected to remain clinically stable for 30
days).
-
no previous exposure to antiangiogenic therapies
-
no chemotherapy within 14 days of trial entry
-
no radiation therapy administered within 21 days
of trial entry
-
corticosteroids and non-steroidal
anti-inflammatory agents ok to continue if
patient has been receiving for >14 days at time
of study entry
|
Trial Support/Funding Includes:
-
Antiangiogenic peptide provided at no charge
-
Biopsy (as required at trial initiation,
date of first objective response and date of
relapse)
-
MRI at study entry, and every 3 months
through Day 180 for selected patients
All patients must be evaluated and treated
through a participating Animal Cancer Institute
Network site, monthly.
Diagnostic and staging tests may be performed at
any veterinary hospital within 10 days of
initiation (full serum chemistry, CBC, U/A and
thoracic radiographs).
Dogs will receive a supply of medication for
in-home, daily subcutaneous injection or will be
treated at a representative clinic every 14 days
with a depot injection. Continued therapy will
be available pending response to therapy.
All examination, tumor imaging and other
diagnostic costs are patient?s responsibility.
Cases which relapse or are refractory following
>30 days on antiangiogenic therapy will be
eligible to receive open label gemcitabine
therapy. Gemcitabine will be provided at no
charge - all other costs associated with drug
examination and drug administration will be
owner responsibility. Assessment of response
will be made following the first cycle of
therapy and consideration for a
2nd cycle will be made based on patient
response.
|
__________________________________________________________

Participants Needed for Genetics Study of Canine
Osteosarcoma
|
The Animal Cancer Institute in cooperation with
the AMC Cancer Research Center is looking for
assistance in a canine cancer research study.
The project involves collection of
histopathology samples on purebred dogs with
osteosarcoma. The purpose of the analysis is to
determine how genes impact the development of
osteosarcoma in dogs.
|
|
Study eligibility criteria include:
-
Golden Retrievers, Rottweilers, Scottish
Deerhounds and Mastiffs with known pedigrees
can participate in this study. Other breeds
may be eligible upon approval by the Animal
Cancer Institute.
-
Dogs must have a diagnosis of appendicular
osteosarcoma (Grades I-II), with no evidence
of metastatic disease.
-
There must be at least two unaffected
first-degree relatives of the affected dog
(parents, siblings, or offspring) that will
consent to participation through the
donation of 10-15 ml of EDTA-anticoagulated
blood (samples from unaffected relatives are
not required at the time of diagnosis or
sample submission from the affected
patient).
-
Informed owner consent form authorizing
pre-treatment excisional biopsy (to be
collected in a medium supplied by the AMC),
and commitment for treatment with an
acceptable protocol (e.g. amputation or
limb-sparing surgery and systemic
chemotherapy with Cisplatin, Carboplatin,
Adriamycin, or a combination thereof).
Trial Support/Funding Includes:
For more information please contact Jen Turner at
the Animal Cancer Institute (202) 363-7300 or see
our website at:
www.animalcancerinstitute.com |
__________________________________________________________

Patient Disease: Canine Oral Malignant Melanoma
Study Name: Melanoma Vaccine Study
Purpose of the Study: The purpose of this study is to determine if
stimulating a patient's immune system in a very specific way will
prolong survival times in dogs with oral melanoma. Also, to
determine
if this specific immune system stimulation will inhibit new blood
vessel formation in the tumour environment.
Patient Entry Criteria: In general, these studies are available to
qualifying patients living within 100 miles of the Animal Cancer
Centre
at Colorado State University. The patient must have the disease of
oral melanoma which has been confirmed by biopsy. The disease may
have
spread to area lymphnodes, but must not have spread to the lungs.
The
oral melanoma tumour masses must be accessible for therapeutic
injection and surgical removal. No other medical conditions may be
present that might limit the patient's life. The patient is not
allowed to have received radiation therapy or any chemotherapy prior
to
presentation. No additional medication may be given once the
patient
is enrolled into the study. For more information regarding entry
criteria, please contact the Consult Coordinator at 970-297-4195.
Owner Responsibilities: The client must allow a biopsy to be
performed
prior to admission into the study to confirm the diagnosis of oral
melanoma. After the initial diagnostic visit, the client is
required
to bring the patient to regularly scheduled visits for treatment and
rechecks (on two occasions, visits will be four days apart) for up
to a
year after treatment. At each visit of the treatment phase, the
patient may receive sedatives or general anesthesia to facilitate
therapy. No additional medication may be given once the patient is
enrolled into the study.
Financial Incentives: The owner pays for the initial diagnostic
work
up. The study pays for all treatment visits and for any adverse
events that may occur as a direct result of the treatment
injections.
Additionally, the study will pay $750 toward the cost of surgical
removal of the tumour. It is required that the tumour be surgically
removed during the course of therapy. For more information
regarding
financial incentives, please contact the Consult Coordinator at
970-297-4195.
Purpose of the Study: The purpose of this study is to determine if
stimulating a patient's immune system in a very specific way will
prolong survival times in dogs with oral melanoma. Also, to
determine if this specific immune system stimulation will inhibit
new blood vessel formation in the tumour environment.
_______________________________________________________________

Patient Disease: Canine Cancer Patients
Study Name: Chemotherapy and Its Effect on Adaptive Immunity
Purpose of the Study: The purpose of this study is to evaluate how
the immune system is affected by chemotherapeutic agents.
Patient Entry Criteria: In general, these studies are available to
qualifying patients living within 100 miles of the Animal Cancer
Centre at Colorado State University. Eligible patients are canine
cancer patients beginning specific chemotherapy protocols. The
patient must be prescribed to begin one of the following
chemotherapy protocols: Adriamycin alone; Madison-Wisconsin
multi-drug protocol; or specific protocols involving
carboplatin, or cisplatin. Patients may not have
received chemotherapy or steroids within two weeks of starting this
study. Additionally, patients may not have concurrent disease that
might prevent them from completing the study.
Owner Responsibilities: This study pays only the cost of blood
tests related to the study. The client is responsible for all costs
related to the treatment of the patient's cancer, and for all costs
related to complications that might arise as a result of treatment
of the patient's cancer. All blood samples related to the study
must be collected at the Animal Cancer Centre.
Financial Incentives: This study pays the cost of blood tests
related to the study. For more information regarding financial
incentives, please contact the Consult Coordinator at 970-297-4195.
__________________________________________________________

Patient Disease: Canine patients with soft tissue sarcoma.
Study Name: Canine Soft Tissue Sarcoma Vaccine Study
Purpose of the study: The purpose of this study is to evaluate the
effectiveness, and to establish the most appropriate dose of a
vaccine intended to inhibit the growth of new blood vessels in
tumours. The vaccine is prepared using the DNA from human blood
vessel growth factors. Using this specially prepared vaccine, we
hope to stimulate a canine patient's immune system to make
antibodies against newly forming blood vessels in a tumor.
Patient Entry Criteria: In general, these studies are available to
qualifying patients living within 100 miles of the Animal Cancer
Center at Colorado State University. The patient must have the
disease of soft tissue sarcoma, which has been confirmed by biopsy.
The soft tissue sarcoma must be measurable and accessible to biopsy.
The disease may not have spread to any other area of the body. In
order to qualify for this study, treatment prior to presentation to
the Animal Cancer Centre must have been very limited. The patient is
not to have received radiation therapy, any chemotherapy, or any
holistic medical treatment for soft tissue sarcoma prior to entry
into the study. The patient must not have received steroids (like
prednisone) or NSAIDs (like carprofen) for four weeks before
presentation. No other medical conditions may be present that might
limit the patient's life. And no additional medication may be given
once the patient is enrolled into the study. For more information
regarding entry criteria, please contact our Consult Coordinator at
970-297-4195.
Owner Responsibilities: After the initial diagnostic visit, the
client is required to bring the patient to regularly scheduled
visits for treatment and evaluation for up to a year. The client
must allow a total of three biopsies to be taken (one pre-treatment
and two during treatment) to assess the patientís response to the
vaccine. These biopsy procedures require the patient to be
profoundly sedated or anesthetized. No additional medication may be
given once the patient is enrolled into the study. Procedures or
treatments unrelated to the study will be the owner's financial
responsibility.
Financial Incentives: The owner pays for the initial diagnostic
work up, usually $300 to $400. The study pays for all treatment
procedures and for all evaluation recheck visits for a period of one
year. For more information regarding financial incentives, please
contact our Consult Coordinator at 970-297-4195.
________________________________________________________

Patient Disease: Canine patients with melanoma, hemangiosarcoma,
or
osteosarcoma
Study Name: Interferon Tau Study
Purpose of the study: The purpose of this study is to collect
tolerability (toxicity), immune response and preliminary
effectiveness information for the administration of Interferon Tau
in canine cancer patients. The information generated by this study
will then be used to design a larger study comparing
standard-of-care therapy to standard-of-care therapy plus Interferon
Tau.
Patient Entry Criteria: In general, these studies are available to
qualifying patients living within 100 miles of the Animal Cancer
Center at Colorado State University. Eligible patients are canine
cancer patients with melanoma, hemangiosarcoma, or osteosarcoma.
When the patient has exhausted all standard-of-care therapy options,
or the client declines standard-of-care therapy, the client will be
offered entry into this study. Dogs which stage positive for
metastasis are considered eligible. Once entered into the trial, an
owner may elect, at any time, to discontinue with the trial and seek
other treatment.
Owner Responsibilities: The client is responsible for all costs
related to the diagnosis and treatment of the patientís cancer, and
for all costs related to complications that might arise as a result
of treatment of the patientís cancer. All evaluations and blood
samples related to the study must be collected at the Animal Cancer
Center. All patients will be evaluated two weeks following the
initiation of therapy and then at monthly intervals.
Financial Incentives: This study pays only the cost of Interferon
Tau. For more information regarding financial incentives, please
contact our Consult Coordinator at 970-297-4195.
___________________________________________________________

Patient Disease: Canine Hemangiosarcoma of the Spleen
Study Name: Hemangiosarcoma Metronomic Chemotherapy Study
Purpose of the study: The purpose of this study is to evaluate the
effectiveness of metronomic chemotherapy for the treatment of canine
splenic hemangiosarcoma. Metronomic chemotherapy is a method of
delivering chemotherapeutic agents at lower doses, but administering
the doses more often. This study is designed as a randomized
clinical trial. There are two treatment groups. One group receives
doxorubicin (Adriamycin®) chemotherapy every two weeks for five
treatments. The other group receives metronomic chemotherapy using
etoposide, cyclophosphamide, and piroxicam.
Patient Entry Criteria: In general, these studies are available to
qualifying patients living within 100 miles of the Animal Cancer
Center at Colorado State University. The patient must have the
disease of hemangiosarcoma of the spleen, which has been confirmed
by biopsy and histopathology. The spleen must be surgically removed
and the disease may not have spread to any other area of the body.
In order to qualify for this study, the patient is not to have
received radiation therapy,
any chemotherapy, or any holistic medical treatment for splenic
hemangiosarcoma prior to entry into the study. The patient must not
have received steroids (like prednisone) for three weeks prior to
presentation. No other medical conditions may be present that might
prevent the patient from completing the study. And no additional
medication related to the disease may be given once the patient is
enrolled into the study. For more information regarding entry
criteria, please contact our Consult Coordinator at 970-297-4195.
Owner Responsibilities:
This study requires frequents visits to the Animal Cancer Center.
The client must schedule and keep all appointments related to the
study. Should the owner decide to withdraw from the study, the owner
assumes responsibility for all costs incurred.
Financial Incentives: The owner pays for the initial diagnosis and
surgical treatment of the disease. Additionally, the owner is
responsible for the cost of the staging tests used to determine if
the patient meets the eligibility requirements of the study (usually
about $600). Once eligible, the study pays for all study-related
examinations, tests, and chemotherapy treatments for up to one year.
For more information regarding financial incentives, please contact
our Consult Coordinator at 970-297-4195.
____________________________________________________________

Patient Disease: Canine Soft Tissue Sarcoma
Study Name: Soft Tissue Sarcoma Heat and Radiation Perfusion Study
Purpose of the study: Localized hyperthermia (heat) combined with
radiation has been shown to be an effective treatment to control
soft tissue sarcoma. The purpose of this study is to discover the
mechanism of how localized hyperthermia enhances the effects of
radiation therapy.
Patient Entry Criteria: In general, these studies are available to
qualifying patients living within 100 miles of the Animal Cancer
Center at Colorado State University. The patient must have the
disease of soft tissue sarcoma, which has been confirmed by biopsy
and histopathology. No other medical conditions may be present that
might prevent the patient from completing this six-week study. For
more information regarding entry criteria, please contact our
Consult Coordinator at 970-297-4195.
Owner Responsibilities: This study requires six weeks of frequents
visits to the Animal CancerCentre. The patient will receive daily
treatments (M-F) for five weeks of the six-week protocol. The client
must schedule and keep all appointments related to the study. Should
the owner decide to withdraw from the study, the owner
may be held responsible for all costs
incurred.
Financial Incentives: The owner pays an initial $250. The study
pays all remaining costs associated with initial diagnostics,
hyperthermia treatment, radiation therapy, and all costs associated
with complications resulting from treatment. Costs associated with
tumor recurrence, metastasis, routine health maintenance, or any
treatment beyond hyperthermia and radiation intended for tumor
control are the responsibility of the owner. For more information
regarding financial incentives, please contact our Consult
Coordinator at 970-297-4195.
_______________________________________________________________

Patient Disease: Canine Osteosarcoma of a Limb
Study Name: Osteosarcoma and Meloxicam Study
Purpose of the study: The purpose of this study is to evaluate the
benefits of the drug meloxicam inthe postoperative pain management
of canine patients with osteosarcoma.
Patient Entry Criteria: In general, these studies are available to
qualifying patients living within 100 miles of the Animal Cancer
Centere at Colorado Sate University. Eligible patients are dogs with
histologically confirmed osteosarcoma of an extremity. The patientís
treatment plan must include amputation of the effected limb followed
by doxorubicin (Adriamycin®) chemotherapy. Diagnostic evaluation
must indicate no spread of cancer in the patient. Additionally, the
patient must have no pre-existing heart condition that would make
doxorubicin an inappropriate choice for treatment. Patients may not
have concurrent disease that might prevent them from completing the
study.
Owner Responsibilities: This study pays only the cost of meloxicam.
The client is responsible for all costs related to the diagnosis and
treatment of the patientís cancer, and for all costs related to
complications that might arise as a result of treatment of the
patient's cancer.
Financial Incentives: This study pays only the cost of meloxicam.
_______________________________________________________________

Participants Needed for Genetics Study of Canine Osteosarcoma/x-tad-bigger>/bigger>/bigger>/bigger>/fontfamily>
Animal Cancer Institute Trials/bigger>/bigger>/color>/fontfamily>
Since its inception the
Animal Cancer Institute and its Network of veterinary oncologists
have offered cutting edge treatment options to the metropolitan D.C.
area. In the last six months the Animal Cancer Institute Network has
expanded across the United States, with newly active treatment sites
in New York, Florida, Texas, and California./x-tad-bigger>/fontfamily>
It is the goal of the
Animal Cancer Institute to provide more effective and less toxic
options for the treatment of cancer. Collaboration with the
pharmaceutical industry allows these options to be provided, in many
cases at no cost. For more information on the Animal Cancer
Institute, visit our website at:
/x-tad-bigger>
www.animalcancerinstitute.com/x-tad-bigger>/color>. /x-tad-bigger>/fontfamily>
/x-tad-bigger>
The Animal Cancer Institute, LLC/bigger>/bigger>/fontfamily>
Cutting edge options
for cancer/x-tad-bigger>/fontfamily>
C. Khanna DVM, PhD, DACVIM/fontfamily>
T. Rusk DVM/fontfamily>
For more information contact Jennifer
Turner/fontfamily>
Phone: 202-363-7300/fontfamily>
Fax: 202-363-7126/fontfamily>
Email:
jturner@animalcancerinstitute.com/color> /fontfamily>
You may register your
clinic to receive electronic updates on trials available to your
clients. Registration for eTrial Updates is available at our
website, /x-tad-bigger>
www.animalcancerinstitute.com/x-tad-bigger>/color>./x-tad-bigger>/fontfamily>
The Animal Cancer
Institute in cooperation with the AMC Cancer Research Center is
looking for assistance in a canine cancer research study. The
project involves collection of histopathology samples on purebred
dogs with osteosarcoma. The purpose of the analysis is to determine
how genes impact the development of osteosarcoma in dogs./x-tad-bigger>/fontfamily>
Study eligibility criteria
include:/x-tad-bigger>/fontfamily>
• Golden Retrievers,
Rottweilers, Scottish Deerhounds and Mastiffs with known pedigrees
can participate in this study. Other breeds may be eligible upon
approval by the Animal Cancer Institute./x-tad-bigger>/fontfamily>
• Dogs must have a
diagnosis of appendicular osteosarcoma (Grades I-II), with no
evidence of metastatic disease./x-tad-bigger>/fontfamily>
• There must be at least
two unaffected first-degree relatives of the affected dog (parents,
siblings, or offspring) that will consent to participation through
the donation of 10-15 ml of EDTA-anticoagulated blood (samples from
unaffected relatives are not required at the time of diagnosis or
sample submission from the affected patient)./x-tad-bigger>/fontfamily>
• Informed owner consent
form authorizing pre-treatment excisional biopsy (to be collected in
a medium supplied by the AMC), and commitment for treatment with an
acceptable protocol (e.g. amputation or limb-sparing surgery and
systemic chemotherapy with Cisplatin, Carboplatin, Adriamycin, or a
combination thereof)./x-tad-bigger>/fontfamily>
Trial Support/Funding
Includes:/x-tad-bigger>/fontfamily>
• $150 stipend toward cost
of biopsy • Histopathology and shipping of samples (an approximate
value of $130) will be performed at no charge by the AMC Cancer
Research Center ./x-tad-bigger>/fontfamily>
For more information
please contact Jen Turner at the Animal Cancer Institute (202)
363-7300 or see our website at:
/x-tad-bigger>
www.animalcancerinstitute.com/x-tad-bigger>/color>/fontfamily>
________________________________________________________

Antiangiogenic Therapy for Dogs with Measurable Soft
Tissue Sarcomas/x-tad-bigger>/bigger>/bigger>/bigger>/fontfamily>
Animal Cancer Institute Studies/bigger>/bigger>/color>/fontfamily>
Since its inception
the Animal Cancer Institute and its Network of veterinary
oncologists have offered cutting edge treatment options. The
Animal Cancer Institute Network is based in Washington, DC and
extends across the United States with sites in California,
Connecticut, Florida, Maryland, Massachusetts, New Jersey, New
York, Ohio, Texas, Virginia and Washington ./x-tad-bigger>/fontfamily>
It is the goal of the
Animal Cancer Institute to provide more effective and less toxic
options for the treatment of cancer. Collaboration with the
pharmaceutical industry allows these options to be provided, in
many cases, at substantially reduced costs. For more information
on the therapeutic diet clinical study for cats with lymphoma,
and the Animal Cancer Institute, visit our website at:
/x-tad-bigger>
www.animalcancerinstitute.com/x-tad-bigger>/color>. /x-tad-bigger>/fontfamily>
/x-tad-bigger>
The Animal Cancer Institute, LLC/bigger>/bigger>/fontfamily>
Cutting edge
options for cancer/x-tad-bigger>/fontfamily>
C. Khanna DVM, PhD, DACVIM/fontfamily>
T. Rusk DVM/fontfamily>
Study Monitor– Kate Cadorette/fontfamily>
Phone: 202-363-7300 Fax: 202-363-7126/fontfamily>
Email:
kcadorette@animalcancerinstitute.com/color>/fontfamily>

You may register your clinic to receive electronic updates on
trials available to your clients. Registration for eTrial Updates is
available at our website,
/x-tad-bigger>
www.animalcancerinstitute.com/x-tad-bigger>/color>./x-tad-bigger>/fontfamily>
/fontfamily>
Trial eligibility
criteria include:/x-tad-bigger>/fontfamily>
•
/x-tad-bigger>/x-tad-bigger>client
owned pet dogs/x-tad-bigger>/fontfamily>
• measurable,
histologically confirmed soft tissue sarcomas, not including
hemangiosarcomas/x-tad-bigger>/fontfamily>
• tumors must be
accessible for histopath collection and objective measurement using
direct caliper measurement, ultrasound, radiographs or CT/MRI scan./x-tad-bigger>/fontfamily>
• favorable clinical
performance status at entry (expected to remain clinically stable
for 30 days)./x-tad-bigger>/fontfamily>
• no previous exposure to
antiangiogenic therapies/x-tad-bigger>/fontfamily>
• no chemotherapy within
14 days of trial entry/x-tad-bigger>/fontfamily>
• no radiation therapy
administered within 21 days of trial entry/x-tad-bigger>/fontfamily>
• corticosteroids and
non-steroidal anti-inflammatory agents ok to continue if patient has
been receiving for >14 days at time of study entry/x-tad-bigger>/fontfamily>
/x-tad-bigger>
Trial Support/Funding Includes:/x-tad-bigger>/fontfamily>
•
/x-tad-bigger>/x-tad-bigger>
Antiangiogenic peptide provided at no charge/x-tad-bigger>/fontfamily>
• Biopsy (as required at
trial initiation, date of first objective response and date of
relapse)/x-tad-bigger>/fontfamily>
• MRI at study entry, and
every 3 months through Day 180 for selected patients/x-tad-bigger>/fontfamily>
All patients must be
evaluated and treated through a participating Animal Cancer
Institute Network site, monthly./x-tad-bigger>/fontfamily>
Diagnostic and staging
tests may be performed at any veterinary hospital within 10 days of
initiation (full serum chemistry, CBC, U/A and thoracic
radiographs)./x-tad-bigger>/fontfamily>
Dogs will receive a supply
of medication for in-home, daily subcutaneous injection or will be
treated at a representative clinic every 14 days with a depot
injection. Continued therapy will be available pending response to
therapy./x-tad-bigger>/fontfamily>
/x-tad-bigger>
All examination, tumor imaging and other diagnostic costs are
patient’s responsibility./x-tad-bigger>/fontfamily>
/x-tad-bigger>/fontfamily>
Cases which relapse
or are refractory following >30 days on antiangiogenic therapy will
be eligible to receive open label gemcitabine therapy. Gemcitabine
will be provided at no charge - all other costs associated with drug
examination and drug administration will be owner responsibility.
Assessment of response will be made following the first cycle of
therapy and consideration for a /x-tad-bigger>/fontfamily>
2nd cycle will be made
based on patient response./x-tad-bigger>/fontfamily>
/x-tad-bigger>/fontfamily>
For more information
please contact Kate Cadorette at the Animal Cancer Institute
(202-363-7300) or see our website at
/x-tad-bigger>
www.animalcancerinstitiute.com/x-tad-bigger>/color>./x-tad-bigger>/fontfamily>
________________________________________________________

Oral Antimitotic Agent for Dogs with Lymphoma/bigger>/bigger>/fontfamily>
/fontfamily>
Animal Cancer Institute Studies/bigger>/bigger>/color>/fontfamily>
Since its inception the
Animal Cancer Institute and its Network of veterinary oncologists
have offered cutting edge treatment options. The Animal Cancer
Institute Network is based in Washington, DC and extends across the
United States with sites in California, Connecticut, Florida,
Maryland, Massachusetts, New Jersey, New York, Ohio, Texas, Virginia
and Washington ./x-tad-bigger>/fontfamily>
It is the goal of the
Animal Cancer Institute to provide more effective and less toxic
options for the treatment of cancer. Collaboration with the
pharmaceutical industry allows these options to be provided, in many
cases, at substantially reduced costs. For more information on the
therapeutic diet clinical study for cats with lymphoma, and the
Animal Cancer Institute, visit our website at:
/x-tad-bigger>
www.animalcancerinstitute.com/x-tad-bigger>/color>./x-tad-bigger>/fontfamily>
/x-tad-bigger>
The Animal Cancer Institute, LLC/bigger>/bigger>/fontfamily>
Cutting edge options
for cancer/x-tad-bigger>/fontfamily>
C. Khanna DVM, PhD, DACVIM/fontfamily>
T. Rusk DVM/fontfamily>
For more information, contact /fontfamily>
Jennifer Turner:/fontfamily>
Phone: 202-363-7300 /fontfamily>
Fax: 202-363-7126/fontfamily>
Email:
jturner@animalcancerinstitute.com/color>/fontfamily>
/color>
You may register your clinic to receive electronic updates on trials
available to your clients. Registration for eTrial Updates is
available at our website,
/x-tad-bigger>
www.animalcancerinstitute.com/x-tad-bigger>/color>./x-tad-bigger>/fontfamily>
Oral Antimitotic Agent for Dogs with Lymphoma/x-tad-bigger>/bigger>/bigger>/bigger>/fontfamily>
Eligibility
Criteria Include:/x-tad-bigger>/fontfamily>
• measurable,
cytologically diagnosed NH lymphoma (histology collected at
study entry)/x-tad-bigger>/fontfamily>
• any clinical stage
but must have nodal involvement- includes relapsed cases/x-tad-bigger>/fontfamily>
• favorable
performance score/x-tad-bigger>/fontfamily>
• no concurrent
chemotherapy (within 14 days of trial entry)/x-tad-bigger>/fontfamily>
• no concurrent
radiation therapy (within 21 days of trial entry)/x-tad-bigger>/fontfamily>
• concurrent use of
corticosteroids accepted providing treatment duration is greater
than 21 days and/or no clinical improvement is noted. Measurable
disease defined by examination, radiographs, ultra-sound, CT or
MRI scan/x-tad-bigger>/fontfamily>
/x-tad-bigger>
Trial Design: /x-tad-bigger>/fontfamily>
Diagnostic and staging
tests may be performed at any veterinary hospital within 10 days
of initiation of study:/x-tad-bigger>/fontfamily>
• Serum biochemistry/x-tad-bigger>/fontfamily>
• CBC/x-tad-bigger>/fontfamily>
• Urinalysis/x-tad-bigger>/fontfamily>
• Thoracic and
abdominal radiographs/x-tad-bigger>/fontfamily>
Patients will be
treated at a participating Animal Cancer Institute Network
clinic. Lymph node biopsies will be required at entry, Day 7,
first objective response and at progression or relapse./x-tad-bigger>/fontfamily>
/x-tad-bigger>
Trial Support/Funding Includes:/x-tad-bigger> /fontfamily>
• /x-tad-bigger>
Laboratory, biopsy and professional fees (as required for the
study) from time of enrollment through Day 56 (additional
monthly exams beyond Day 56 will be owner’s financial
responsibility)/x-tad-bigger>/fontfamily>
• Oral Antimitotic
agent through Day 56 (beyond Day 56, additional monthly
shipments of study drug supply will be billed to the
clinic/investigator at a rate of $50 per shipment)/x-tad-bigger>/fontfamily>
Dogs will receive the
oral medication over a 4-week initial phase. Continued therapy
will be available pending response to therapy. Long-term
follow-up recheck examinations will be performed monthly./x-tad-bigger>/fontfamily>
For more information
please contact the Animal Cancer Institute (202-363-7300) or see
our website at /x-tad-bigger>
www.animalcancerinstitiute.com/x-tad-bigger>/color>./x-tad-bigger>/fontfamily>
|
Hello everyone.
I have been asked to pass on this very important information.
Dr. Edmund Sullivan, who you may recall, is the wonderful vet from
Bellingham Veterinary Critical Care, who did Comet's bone marrow
transplant, is now working with a company called Leuchemix, that is
developing a new drug to treat acute myeloid and acute lymphoblastic
leukemia, two conditions that are often rapidly fatal.
In order to test the in vitro effectiveness of the drug being developed by Leuchemix, Dr. Sullivan
and his team, need fresh whole blood or marrow samples from dogs with
either of these conditions.
If in vitro effectiveness can be established, then a clinical trial will
be set up for dogs with these conditions.
If anyone has questions about this in vitro study, they can contact Dr.
Sullivan at the email address or phone numbers listed below.
Edmund Sullivan, DVM
Bellingham Veterinary
720 Virginia St
Bellingham WA 98225
360-734-0720
360-220-6083
bvcc720@yahoo.com
Thank you very much for your help. Together, we can make a difference,
and take a bite out of canine cancer.
You are welcome to cross post this information, and updates will be
posted on Blues' web site, at www.smilingblueskies.com, in Dr.
Sullivan's special section.
You are also welcome to contact Dr. Sullivan directly. |
|
We all remember the
story of Comet.
Well, there have been nearly 100 dogs treated for lymphoma with a bone
marrow transplant (Actually, the process is stem cell therapy, since
there is no collection of actual bone marrow, but rather, the stem cells
that reside in the marrow are removed.) during the last 10 years. Most
of these patients were treated at North Carolina State University, and
the remainder were treated in Bellingham, and two private practices
located in Los Angeles and San Diego.
Of all these patients, approximately 40 percent have been long term
survivors, that is, free of lymphoma for at least 2 years.
Comet and Annabelle, two of the very first transplant patients, lived
out the remainder of their lives, free of lymphoma!
Some of the patients who relapsed following the bone marrow transplant,
responded well to rescue therapy, and have been surviving up to 2 years.
Dr. Sullivan told me that there have also been significant improvements
in the transplant process itself. Currently, they have an optimal
treatment protocol. This protocol involves early planning for a
transplant, best done during the first remission, which is usually 6 to
8 weeks following induction chemotherapy, as this allows for a better
outcome and reduces the overall cost of lymphoma therapy in general,
since the bone marrow transplant process is a definitive therapy that
does not require long term chemotherapy.
Further, they identify a tumor marker prior to treatment, to confirm
molecular remission, and the medications used to optimize the stem cell
collection have also been improved. The machine used for the stem cell
collection, called an apheresis machine, has been updated too.
Notably, the process is also significantly less expensive that it was 10
years ago. While it was about $40,000 ten years ago, today, the cost is
$12,000 to $15,000 US, depending on the size of the dog.
In addition, over the last 8 months, a special service has been put into
place, for the identification of related bone marrow donors for
allogenic transplants. |
Wednesday, April 6, 2005
What price a pet's life? $45,000 to treat Comet/bigger>
|
Here is an Update on
Comet's Progress, 21 Months Since His Original Diagnosis,
and 15 Months Since
his Bone Marrow Transplant
Comet has been doing
very well and is currently off all medications related to
his transplant. He has no signs of graft versus host disease, is
apparently free of lymphoma, and has sustained engraftment. He runs
five miles every day with his owner and other Golden Retriever
companion, Ajax. This month is 21 months since his original
diagnosis and 15 months since his transplant.
Dr. Westfall and Dr.
Sullivan, continue working towards providing transplants for
additional patients, and they have 8 patients with lymphoma being
staged for both allogenic and autologous transplants. Currently,
the cost for an autologous transplant is expected to be around $12K
US and an allogenic transplant between $18-20K depending upon the
size of the dog, the number of matching studies, and the length of
hospitalization. The doctors hope that these costs will continue to
decline as they learn more and streamline the process. With an
autologous transplant they expect to have long term disease free
periods in 30% of these patients. With allogenic transplants with
matching DLA donors (sibling donors), they expect up to 60% long
term disease free periods. These numbers are estimates based
upon the results of autologous transplants done 25 years ago
adjusted for improvements in chemo protocols and supportive care
post transplant.
It is important that
staging for the transplants be started as soon after the initial
diagnosis as possible since autologous transplants are best done in
the first remission. Also, the use of Neupogen and un-irradiated
blood products before the transplant can interfere with mobilization
and engraftment.
|
"Comet is like many Golden Retrievers: gentle, devoted,
enthusiastically greeting each day wih his wagging, plumed
tail. He loves to swim, run in the woods and pack around his
large toy hamburger.
But Comet is different. He's one of very few dogs worldwide
to receive a stem-cell transplant for cancer treatment,
rather than primarily for research. Cost of the therapy:
$45,000.
Visit the following link, to read more about the miraculous
story of Comet, the Golden Retriever, written by Warren
King, Seattle Times Medical Reporter. (Permission has been
granted by the Seattle Times, to post this link.
http://seattletimes.nwsource.com/html/localnews/2002232414_dogtransplant06m.html/color>/fontfamily>
Drs. Edmund Sullivan and Theresa Westfall,
Veterinarians at Bellingham Veterinary & Critical Care
Bellingham, Washington
Drs. Edmund Sullivan and Theresa Westfall, veterinarians at
Bellingham Veterinary & Critical Care, located in
Bellingham, Washington, have been extraordinary at "pushing
the envelope", trying to get treatment for desperately sick
animals. They have been working with the researchers at the
Fred
Hutchinson Cancer Research Center, located in Seattle,
Washington, a world renowned facility for cancer treatment.
People come from all over the world, to be treated at FHCRC.
You can visit the centre on line, at
http://www.fhcrc.org/
Many of you may be familiar with the FHCRC, because of the
work they have been doing to "develop the resources
necessary to map and clone canine genes, in an effort to
utilize dogs as a model system for genetics and cancer
research. The Dog Genome Project is moving from the FHCRC to
the National Human Genome Research Institute, which is part
of the National Institutes of Health, located in Bethesda,
Maryland. The project will change its name to the NHGRI Dog
Genome Project, and will be found on the web at
http://research.nhgri.nih.gov/dog_genome/.
About a year ago, Drs. Sullivan and Westfall and the team at
the FHCRC did a bone marrow transplant on a young Golden
Retriever from San Juan Island named Comet, who was
suffering from T-Cell lymphoma. This was not an experimental
treatment, in the sense that most of the bone marrow
transplant knowledge for humans, has been gained through
work with dogs. However, this was one of the few times, at
least in the United States, that a pet had been given a bone
marrow transplant for lymphoma. Comet is alive and well, and
accompanies his people on a 5 mile run every day. Comet's
"one year anniversary" is coming up in a couple of weeks!
The following, is an excerpt from an email, that was just
shared with a group of Golden Retriever fanciers and
breeders:
"We are currently treating cases of high grade lymphoma (any
subtype is fair game, T Cell, B Cell, lymphoblastic, etc.)
and leukemia. These two groups are known to respond well to
bone marrow transplants--there are literally thousands of
people who have been treated. Comet is evidence that current
knowledge is out there and potentially can be adapted to
treat some of these common forms of cancer in dogs." (Thanks
to Nancy Clifton)
If you have a dog with lymphoma, or know of one, they may be
eligible for this treatment . This is a fantastic
breakthrough. We have all done our homework, and we all know
that there is much more homework to be done, but this opens
the window of hope even further, for our beloved heart dogs.
Contact Information:
Edmund Sullivan, DVM
Theresa Westfall, DVM
Bellingham Veterinary & Critical Care
720 Virginia Street
Bellingham, WA 98225
360-734-0720
360-752-5555 fax
bvcc720@yahoo.com
http://www.skagitvalleyherald.com/articles/2004/04/12/news/news06.txt
You or your veterinarian can call Bellingham Veterinary and
Critical Care, at
360-734-0720. They are located at 720 Virginia Street,
Bellingham, WA, USA, 98225.
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Index of Grants:
Index of Articles:
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To All Friends of Dogs:
It's hard to believe that almost three years have gone by already since Thunder was diagnosed with lymphoma. I remember so many details of that moment: how my weight was shifted to my left leg, the color of my shoes, the feel of Thunder's broad head under my hand, his eyes. I remember his trusting eyes so well. Odd, though, I don't recall much of what was said, just the sound of a voice breaking the news that I'd already guessed. I got through that moment, but never away from it.
If you've had Goldens for very long, or dogs for very long, you know that moment, because you've been there. And if you haven't been there yet, you will be. Sixty to seventy percent of Goldens die of cancer; forty-five percent of all dogs die of cancer. In fact, some of you are hearing the news that your dog has cancer today, and some will hear the news tomorrow, or next week. Right now, that's almost a given if you own multiple dogs.
After Thunder was diagnosed, I searched for answers, the same as everyone else does. How do I help him? Why did this happen? How do I protect my other dogs? I have to admit that my first reaction was centered on MY dogs - I did not immediately see the bigger picture. But what I finally realized was that to help my own dogs, I needed to become part of the bigger picture. The only way to improve the future for my dogs, was to become part of the solution by participating in research to help all dogs.
And I discovered very quickly that helping other dogs, helping my breed, gave meaning to that moment. If I had to lose Thunder, what better legacy could he leave behind, than to be part of a more hopeful future?
I wrote a public letter then, hoping to help recruit others who wanted to do more than just grieve for their impending loss. And so many who read the plea responded. Their willingness to reach out in the midst of their sorrow, really made a difference in a lymphoma study that was in progress at that time. And I'm sure that every owner who participated would affirm that they are grateful they had that opportunity.
Thunder passed away about 2 years ago. The disease got him - but in one small way, he struck a blow against the disease too. That remains a source of comfort.
So here we are, nearly three years later, and I'm writing another letter. There is a new canine cancer study that needs our support and participation. This one is for Goldens, Rottweilers, and Mastiffs who have been diagnosed with lymphoma or osteosarcoma. Other breeds may be included with prior approval of the researchers. Owners and their vet will need to submit biopsy samples, a blood sample, a pedigree, signed consent forms, and agree to acceptable chemotherapy treatment. Blood samples will also be needed from 2 unaffected first degree relatives (parents, siblings, offspring).
Now here's the part that is sometimes a problem: the biopsy sample must be prepared in a very specific way, using a solution supplied by the researchers. Therefore, the researchers must be contacted at least a day or two PRIOR to the surgery. In addition, the dog must not have started treatment such as chemotherapy or prednisone before the biopsy.
We who love our dogs, the scientists trying to help us, and of course, the dogs themselves - need your help. We're all in this together, and together we can make a difference.
If you are faced with that numbing moment when you hear or suspect a diagnosis of lymphoma or osteosarcoma, and your dog fits the study requirements, please contact me. I know it takes courage to look beyond that moment, while you are in the midst of it. But I also know that these affected dogs who participate in research, leave behind a legacy that will
be one of your greatest comforts.
If your dog does not meet the requirements for this study, and you would like to find one that is suitable, I will try to help. Even if you just have questions, I will try to help. Like I said, we're all in this together.
Sincerely,
Rhonda Hovan
rhondahovan@aol.com
330-668-0044
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Current Canine Health Foundation Studies In Cancer

In a recent issue of the
"Golden Retriever News", Rhonda Hovan, breeder/exhibitor/judge
called upon every Golden Retriever Club of America member, to make a
personal financial commitment to support canine health research. Below,
you will find an abstract of each of the grants being carried out by the
Canine Health Foundation, that address an aspect of canine cancer. Each
of these studies holds great promise, not only for Golden Retrievers,
but for all pure breeds, but without sustained commitment from each of
us, studies like these, and studies being carried out right here, at the
University of Guelph's Ontario Veterinary College, will never achieve
their full potential, of being able to provide our dogs, whether pure
breed or mixed breed, with longer, healthier lives.
The Smiling Blue Skies Cancer Fund (Pet Trust: In Memory of Blues) is
one way that you can help make a difference. Every donation you
make to the fund, and every piece of one-of-a-kind art work that you
order, helps us move one step closer to the day, we can truly
laugh in the face of the cruel joke we call cancer.
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Golden Retriever Club of American Foundation
Golden Retriever Research
A Legacy of Hope
With your generous financial support, the Golden Retriever Foundation funds a diverse range of health studies investigating diseases such as several types of cancers, swallowing disorders, cataracts, SAS, and other issues of importance to the breed. In order to succeed, several of these studies require the cooperation of owners and participation of affected dogs -- yet when one's dog is diagnosed with a serious disease, owners may have difficulty recalling details of research studies. Please check back here often, and if you are a subscriber to the "Golden Retriever News", you will find information about research being conducted, in every issue.
For some studies, it is important that the dogs NOT be started on any medications prior to enrollment, or that biopsy or surgical samples be prepared in a specific manner, so please make contact as soon as possible when a diagnosis is suspected. Remember also that dogs owned by people who are not Golden Retriever Club of America members, are also eligible for these studies, and please consider referring other Golden owners when possible. Our Blues, a Canadian Kennel Club registered Golden Retriever, was a participant in one of these very important studies.
We recognize that it takes great courage to look beyond one's own sorrow when a special dog is diagnosed with a devastating disease, and we applaud the owners who participate in these research studies. Sometimes in the midst of sadness, helping to work toward a better future allows our beloved dogs to leave a legacy of hope to the next generation.
For more information, questions, or assistance, regarding the Golden Retriever Foundation's research studies, please contact the Golden Retriever Club of America's Research Faciliatator, Rhonda Hovan. Her email address is rhondahovan@aol.com, and her telephone number is 330-668-0044. Together, we can make a difference.
http://www.goldenretrieverfoundation.org/
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Vaccine studies
for canine malignant melanoma: Vaccine studies for canine malignant melanoma and canine lymphoma are under way at several institutions around the United States, including Tufts University School of Veterinary Medicine, the Animal Medical Centre, the University of Wisconsin, University of Pennsylvania and the National Jewish Medical and Research Centre, in collaboration with private veterinary oncologists in Denver, Colorado.
You can find additional information on canine cancer studies at: http://www.amcny.org
See the clinical trials on the links.
http://www.morrisanimalfoundation.org/currentstudies/canine.asp
http://vmthpub.vetmed.wisc.edu/sa_services/med/oncology/Vaccines.htm
http://vmthpub.vetmed.wisc.edu/sa_services/med/oncology/Oral.htm
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Toronto Star - Sep. 25, 2003. 06:24 AM
Royal treatment for a sick Rover $5M animal hospital to treat cancer Oakville facility to be state of the art
FRANK CALLEJA STAFF REPORTER
A $5 million veterinary emergency hospital being built in Oakville will offer cancer treatment, orthopedic surgery and eventually a CAT scan and MRI
in what is said to be the largest such medical treatment facility for pets in Canada. Construction on the 21,000-square-foot building began yesterday on a site on Bristol Circle, near Winston Churchill Blvd. and the Queen Elizabeth Way, on the Oakville-Mississauga border. "This will be the largest private facility of its kind in Canada and one of the few existing in the world," said Dr. Wolfgang Zenker, veterinarian for
the High Park zoo and one of 20 veterinarians involved in the project. He expects the hospital, due to open next spring, will treat up to 30,000 pets every year. Zenker, a well-known veterinarian in Oakville for 33 years, said the hospital has been eight years in the planning and was inspired by a growing need for a facility that is able to offer leading-edge medical services for pets, including dogs, cats, birds, and more exotic creatures such as rabbits
and reptiles. "With provision for an MRI, a linear accelerator for cancer treatment, and a CAT scan, the hospital will serve as a referral centre for specialists during the day and an emergency treatment centre after hours," Zenker said. Although there is no fee schedule available, rates for procedures will be competitive, he said. "More than 50 per cent of Canadians own pets. We expect owners from across the country and the U.S. will bring their animals here because the specialized services are simply not available anywhere else in the community," he said. "For example, one of the areas we will eventually develop will be for the treatment of cancer, and the hospital will eventually have a linear accelerator which is used in cancer diagnosis." There will be six specialist examination rooms, four treatment rooms, and a hydrotherapy room with a variable-height water tank complete with a treadmill walker for exercising dogs after special operations. Zenker said there will be on-site laboratory blood testing, three operating rooms, x-ray facilities, three wards and 15 kennel suites for post-surgery recovery. There will also be an emergency department with six examination
rooms that will be open all day. The hospital, known as the Mississauga-Oakville Emergency Veterinary Clinic, will be an around-the-clock operation, and have 12 specialists on duty during the day and three emergency veterinarians overnight. "In all, there will be a staff complement of 70 to 80 and we'll add staff, specialists and equipment as the facility grows," said Zenker, who has operated Burloak Animal Clinic, on Lakeshore Rd. W. in Oakville, since 1970. Zenker is a specialist in treating exotic animals, including large cats like tigers and lions. As a youngster, he was known as the boy with the alligator. He raised the alligator until it was about 2 metres long before selling it to a reptile museum in Parry Sound. "We've come a long way in the treatment and understanding of animal care and this new facility will not only help with that care, but also enhance our ability to improve quality of life for pets," he said.
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Cellular Genomics - A Cytogenetic Investigation of Canine Soft Tissue Sarcomas
Matthew Breen, PhD. North Carolina State University
Lay Abstract Excerpt: It has been established that non-random chromosome aberrations are characteristic of specific types of many different human cancers. In the dog the extent and identity of chromosome aberrations associated with specific cancers is still largely unknown. In certain breedsŠ soft tissue sarcomas account for up to 50% of all malignant tumors and thus represent a serious health and welfare issue for those breeds. This research proposes to make use of major recent advances in canine molecular cytogenetics to identify recurrent chromosome aberrations associated with canine soft tissue sarcomas, in particular those of histiocytic origin.
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Characterization of Receptor Tyrosine Kinase Dysfunction in Malignant Histiocytosis
Cheryl London, DVM, PhD: University of California, Davis
Lay Abstract Excerpt: Malignant histiocytosis (MH), while rare in people, occurs frequently in certain breeds of dogs including Golden Retrievers. There is no effective therapy for this disease and nearly all patients die with 2-4 months of diagnosis. The research proposes to evaluate MH tumor specimens for mutations in genes that may contribute to the development of this devastating cancer.
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Growth Signaling Pathways in the Pathogenesis and Treatment of Canine Cancer
Principal Investigator, Stuart Helfand, DVM, School of Veterinary Medicine, University of Wisconsin. Co-Investigator and Contact Person, Jaime Modiano, VMD, PhD, AMC Cancer Research Center
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Transferring Receptor Expression by Canine Brain Tumors
Principal Investigator: Natasha Olby, PhD, North Carolina State University
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The Molecular Cytogenics of Canine Lymphosarcoma: Correlating Chromosomal Changes with Clinical Disease
Principal Investigator, Matthew Breen, PhD, North Carolina State University
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Heritable and Sporadic Genetic Lesions in Canine Lymphoma and Osteosarcoma
Principal Investigator: Jaime Modiano, VMD, PhD, AMC Cancer Research Center
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Identification and Characterization of Genetic Mutations in Canine Mast Cell Tumors
Principal Investigator: Cheryl London, DVM, PhD, University of California, Davis
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K9 Cancer Awareness, Research, and Education
http://www.k9care.org/
The mission of K9 Cancer, Awareness, Research & Education (K9CARE) is a simple one. We have joined together to raise funds for canine cancer research. It is our way of battling a disease that has touched so many. We also plan to provide information about canine cancer and to hopefully make others aware of the importance of this issue. An account has been set up with the Morris Animal Foundation, and for every $2500 deposited, we will be sponsoring a canine cancer research project.
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Canine Cancer Research
Information http://www.goldstockfund.org/cancerresearch.html
Canine Cancer is the leading cause of death in Golden Retrievers. There are dedicated scientists conducting research across the country. Many of these studies need dogs to participate in the research. Many times that participation can be as simple as a blood sample. Others are looking for samples, detailed information and more, from dogs diagnosed with specific types of cancer. We at The Goldstock Fund, want to provide a central location of information on active Canine Cancer Research. Our first priority would be to focus on those studies that involve Golden Retrievers. We realize, however, that other studies being done could impact our breed further down the research line. We also would like to include those studies as time permits. Although some of these studies may have very specific criteria for participation, others will be looking for samples to be used for control groups (i.e. healthy Golden Retrievers). Many of the studies will not be restricted to Golden Retrievers, but will include various other breeds. If you hear of a research study, please mail to: info@goldstockfund.org as we want to include all studies seeking participants. We salute the researchers dedicated to finding cures and answers. We applaud the owners who refuse to let their dogs die in vain, and who have the courage to take the extra step to help these researchers be successful.
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DNA
Sought for Cancer Research Denver's AMC Cancer Research Centre is conducting the study "Heritable and Sporadic Genetic Lesions in Canine Lymphoma and Osteosarcoma." Owners of Golden Retrievers, Rottweilers, and Mastiffs diagnosed with lymphoma or osteosarcoma can assist in this vital research by submitting DNA samples (prerequisites must be met). For the full list of prerequisites and sample instructions, please contact Jaime Modiano, VMD, at 303-239-3408 or modianoj@amc.org. Information and updates will be posted on the AMC Cancer Research Centre web site at www.amc.org.
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Some
clinical trials offer free cancer treatment http://www.heska.com/clinicaltrials/cancertrials.asp
Financial constraints can be daunting, when seeking the best treatment for your dog. Even with pet insurance, the costs for chemotherapy can soar to four figures. Clinical research trials, often performed at veterinary colleges, including Tufts, investigate new methods of cancer diagnosis and treatment. Depending on funding, some programmes don't charge owners for services. Trials focus on different types of cancer, according to the investigator's interests, funding source, and support offered. For example, the Heska Corporation, www.heska.com, manufacturer of animal health products in Fort Collins, Colorado, is enrolling dogs with soft tissue sarcoma or oral malignant melanoma, in clinical trials, to test a gene-based therapy that stimulates the immune system response to the tumour. Tufts is studying new treatments for lymphoma and mast cell tumours, as well as a continuing programme of autologous (dog's own) bone marrow transplant for lymphoma. Contact -- Kelly Reed at Tufts -- 508-839-5395, Ext. 84682. The Veterinary Cancer Society, based in Schaumburg, Illinois, 619-460-2002, lists clinical trials and oncology specialists nationwide at www.vetcancersociety.org. Clinical trials offer the opportunity to receive promising new therapies often in conjunction with traditional care regimens. There is often a financial incentive for owners who might otherwise not be able to afford treatment. Pet owners are given all the options and are supported in their decisions.
Cancer continues to be a major health problem in the United States with dogs and people sharing almost identical death rates from it. Cancer causes approximately one in four human deaths, said Kenneth M. Rassnick, D.V.M., Dip. ACVIM, professor of oncology at the College of Veterinary Medicine at Cornell University in Ithaca, New York. Regardless of age, one in four dogs' deaths is due to cancer. Since cancer registries are not available in veterinary medicine, it is likely this number is even higher.
Resource: Tufts University School of Veterinary Medicine, "Your Dog", A Magazine for Caring Dog Owners, October 2002
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Free
Chemotherapy for Dogs with Lymphoma Free chemotherapy for dogs with lymphoma! Yes - FREE. Beginning
April 15th we begin a clinical trial for dogs with lymphoma. We're
only one of three clinics in the United States, participating in a trial
to help dogs with lymphoma. All costs for patient evaluation and
treatment are at NO CHARGE to the pet owner! Call or email us for
additional details.
For further information, please contact:
Kevin A. Hahn, DVM, PhD
Diplomate ACVIM (Oncology)
Gulf Coast Veterinary Specialists
1111 West Loop South, Suite 150
Houston, TX 77027
Phone Number: (713) 693-1166
Fax Number: (713)693-1167
http://www.gulfcoastvetspec.com
mailto:drhahn@gulfcoastvetspec.com Gulf Coast Veterinary Specialists Chemotherapy Tidbits
http://www.gcvs.com/oncology/pwc/chemoinformation.htm
This link provides a summary of information obtained from the current veterinary
literature and from the personal experiences of Dr. Kevin Hahn. It does NOT replace your regular veterinarian.
However, you are welcome to consult with Dr. Kevin Hahn. Please call
713-693-1166.
This link provides information about the following:
- Principles of Chemotherapy
- When Should Chemotherapy Be Considered?
- Tumour Growth and Response to Chemotherapy
- Pharmacologic Principles of Chemotherapy (Dose Response Curve,
Therapeutic Index, Drug Classes, Resistance to Chemotherapy, Chemotherapy
Protocols, Combinations and Scheduling, Multi-Modal Therapy, Dose
Determination,Administration)
- Chemotherapy Safety Guidelines
- Management of Chemotherapy Side Effects
- Chemotherapy Dosages, Indications, and Adverse Reactions, including,
Asparaginase/Elspar, Carboplatin/Paraplatin, CCNU/ Lomustine, Cisplatin/Platinol,
Cyclophosphamide/Cytoxan, Doxorubicin/ Adriamycin, and Vincristine/Oncovin
- Chemotherapy Dosage Conversion Chart
http://www.gcvs.com/oncology/pwc/chemoinformation.htm
Transferring Receptor Expression by Canine Brain
Tumors Principal Investigator: Natasha Olby, PhD, North Carolina State
University
Abstract: Dogs that are not treated following diagnosis of a brain
tumour survive an average of only two weeks. Treatment with either
surgery and/or radiation can extend their survival to about ten
months. Clearly there is a need for new approaches to treating brain
tumours in dogs if survival is to be improved. In humans, malignant
brain tumours are being treated successfully with toxins targeted
specifically to a marker expressed by tumour cells: the transferrin
receptor. In preliminary work, we have shown that untreated canine
brain tumours also express this marker. The primary aim of this
project is to establish whether brain tumours that have recurred
following treatment with radiation or surgery still express the
transferrin receptor. This information will allow us to determine
whether transferrin receptor targeted toxins should be used as the
primary form of treatment of brain tumours, or can be used to treat
recurrent tumours following more conventional therapy. We hypothesize
that brain tumours will express transferrin receptors at high levels
after treatment and therefore that transferrin-linked therapy can be
instituted in combination with more conventional therapy.
Final Report: Immunohistochemical staining for transferrin receptors
has been completed on brain tumours from 80 dogs. Analysis indicates
that transferrin receptors were expressed by all of the tumours. In
addition, collaboration with another group led to investigation of the
expression of insulin-like growth factor-1 receptor (IFG-1R), and it
was determined that IFG-1R is also expressed very strongly in certain
types of brain cancers. This study also determined that a third
receptor (EGFR), is also expressed on many of the brain tumours. Each
of the various receptors that are expressed in different types of
brain cancers may lead to therapies targeted specifically to those
cancers.
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Grants
CHF Grant # X65:
Identification and Characterization of Genetic Mutations in Canine Mast Cell Tumours Principal Investigator: Cheryl London, DVM, PhD; University of California, Davis
The most common malignant tumour in dogs is the mast cell tumour (MCT, a form of skin cancer), occurring with an incidence of close to 20% in the canine population. MCTs range from relatively benign to extremely aggressive, leading to tumour spread and eventual death. Particular breeds of dog are at risk for the development of this tumour, indicating a role for genetic factors. We have previously identified mutations in the gene c-kit in 30-50% of dog MCTs. c-Kit plays a critical role in regulating the growth and function of normal mast cells, and as the mutations we discovered cause uncontrolled function of c-kit, it is likely they influence MCT development in dogs. This proposal will establish a prospective tumour registry of dog MCTs to be used for investigation of the true incidence of c-kit mutations within specific dog breeds. Moreover, the studied outlined in this grant will identify additional genetic mutations present in dog MCTs that can be used for the development of new targeted therapeutics. In summary, this work will provide a much more detailed understanding of dog MCTs, thereby building a framework for the development of new therapies and strategies for disease prevention.
Start date and duration: January, 2003, for two years
Recruitment is beginning for this study. Golden Retrievers affected with mast cell tumour(s) are eligible, and several tissue samples prepared in a specific way are required.
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CHF
Grant # 1626 Significance of Tumour Suppressor Genes in Canine Cancer Principal Investigator: Jaime Modiano, VMD, PhD AMC Cancer Research Centre
Lymphomas and leukemias (cancer of white blood cells), and melanomas (tumours
of pigmented cells responsible for skin colouring) are among the most
common cancers of dogs. These tumours can occur in any breed. However, lymphoma and leukemia are especially common in Golden
Retrievers and Boxers, and melanoma is seen more often in Irish and
Gordon Setters, Standard and Miniature Schnauzers, Doberman Pinschers,
and Scottish Terriers, suggesting that these diseases may have a
hereditary component. Like other tumours, lymphoma, leukemia, and melanoma arise from cells
that grow in an uncontrolled fashion. Normally, tumour suppressor
genes would constrain or eliminate these renegade cells, but mutation
can disable these genes in cancer cells, contributing to the
development and progression of cancer. This laboratory has
characterized the mechanisms that control tumour suppressor gene
function in canine cells. For these studies, the frequency of
mutations of two important tumour suppressor genes in canine melanoma
and lymphoma, will be examined. This will enable them, to
determine the relationship of tumour suppressor gene mutations with
the prevalence of these cancers in high-risk breeds, as well as with
prognosis and outcome. The results from the studies will provide tools
that may predict the risk of a dog or its offspring to develop these
devastating tumours. This information could have an immediate,
visible, and long-lasting impact on canine health, when used
judiciously for breeding decisions. Additionally, it may be useful in
the future, by paving the way towards the development of advanced
molecular therapies for canine cancer.
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CHF Grant # 2025
Growth Signaling Pathways in the Pathogenesis and Treatment of Canine
Cancer Principal Investigator: Stuart Helfand, DVM School of Veterinary Medicine, University of Wisconsin Co-Investigator and Contact Person: Jaime Modiano, VMD, PhD AMC Cancer Research Centre
Hemangiosarcoma (HSA) is a common cancer in dogs that originates from
cells lining the blood vessels. HSA can affect any dog, but is seen
more often in German Shepherds, Skye Terriers, and Golden Retrievers.
This suggests that this disease has a heritable component. Tumours
arise when cells respond inappropriately to growth factors, allowing
them to divide continuously in an uncontrolled fashion. Tumour
suppressor genes contain or eliminate these rapidly dividing cells,
but mutations in these genes can disable their ability to function
correctly. This laboratory is examining the idea that the loss
of function of one of these tumour suppressor genes, PTEN, leads to
the increased production of tumour growth factors. In their studies,
they will examine the frequency of the mutations in the PTEN gene from
dogs with HSA, and the relationship of these mutations to increased
production of a specific tumour growth factor, VEGF. The results of
their research could lead to tests for screening dogs for mutations in
PTEN, and information could have an immediate and long-lasting impact
on canine health when used judiciously for breeding decisions. They
will also test the function within these cells, as a treatment for HSA.
Such work may lead the way for the further development of novel
therapies for the treatment of canine hemangiosarcoma.
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CHF Grant #2038:
The Molecular Cytogenics of Canine
Lymphosarcoma: Correlating Chromosomal Changes with Clinical Disease Principal Investigator: Robert Dunstan, DVM, MS Texas A & M University Co-investigator: Matthew Breen, PhD Animal Health Trust, Great Britain
Cancer kills. Twenty years ago, the diagnosis of lymphosarcoma
(a tumour of the lymph glands) in humans was almost invariably fatal.
However, with the development of improved means to sub-classify this
neoplasm and the tailoring of therapies that are subtype-specific,
more and more forms of lymphosarcoma are treatable. One of the
most important means of sub-classification of human tumours is based
on the identification of chromosome abnormalities. In the dog,
lymphosarcoma comprises one in five malignancies; however, the
extent and identity of chromosome aberrations is still unknown.
This is largely because the chromosomes of dogs were extremely
difficult to identify with confidence. Recently, we have
developed a set of canine chromosome-specific reagents that allow us
to identify conclusively every dog chromosome. We propose to use
these reagents to identify the chromosome aberrations associated with
dog lymphosarcoma and to investigate the correlation between these
aberrations and the clinical disease. Such an approach offers a
means to potentially sub-divide this diverse disease in dogs, thereby
offering new information of diagnosis, prognosis, and therapy.
Identification of specific chromosome aberrations will also help to
investigate the correlation between the genetic etiologies in dogs
with those in humans.
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CHF Grant # 2254
Heritable and Sporadic Genetic Lesions in Canine Lymphoma and
Osteosarcoma Principal Investigator: Jaime Modiano, VMD, PhD AMC Cancer Research Centre
Lymphoma (cancer of the lymph glands) and osteosarcoma (bone cancer)
are two common cancers of dogs with remarkable breed predisposition.
Lymphoma accounts for approximately 20% of all canine tumours, and
greater than 80% of cancer originating from blood cells. Osteosarcoma
is the most common bone tumour in dogs, accounting for 85% of skeletal
cancers. All cancers have a genetic basis, and in effect, these
conditions represent various diseases, each sharing one or a few
genetic abnormalities that contributes to overall risk and treatment
response. However, a means does not exist to identify individual
genes and larger regions within the genome that appear to be important
in canine cancer. For this project, we propose to confirm the
frequency and significance of these genetic anomalies in lymphoma and
osteosarcoma of Golden Retrievers, Rottweilers, Irish Setters, and
Bernese Mountain Dogs. This work will begin to determine which of
these anomalies may be heritable and which may be sporadic, and pave
the way to apply this knowledge for clinical benefits by providing
potential targets for treatment, and tools to determine individual
risk to develop these types of cancer or produce cancer-prone progeny.
This study has enrolled 24 dogs affected with
lymphoma (LSA) and 18 dogs affected with osteosarcoma (OSA), and their
first degree relatives. DNA from these tumours has been examined using
molecular cytogenetics (comparative genomic hybridization, or CGH.),
exploring the loss or amplification of selected oncogenes and tumour
suppressor genes (including p16, Rb, and PTEN). Preliminary data
indicate that the Rb tumour suppressor pathway is inactivated in all
cases of LSA, and is inactivated or compromised in all OSA cases.
Collaborations resulting from this study are ongoing with several
researchers, which permits maximum utilization resources. Intriguing
data is being generated that may help owners and treating
veterinarians make treatment decisions based on breed specific risks.
Recruitment for this study is ongoing. Owners of Goldens with lymphoma
or osteosarcoma are urged to participate. The owner will need to
submit biopsy samples, a blood sample, a pedigree, a signed consent
form, and agree to acceptable chemotherapy treatment. Blood samples
will also be needed from 2 unaffected first degree relatives (parents,
siblings, offspring). The biopsy sample must be prepared in a very
specific way, using a solution supplied by the researchers in advance.
Therefore, the researchers must be contacted at least a day or two
PRIOR to the surgery. This minor delay will not adversely affect the
outcome for the dog. In addition, the dog must not have started
treatment such as chemotherapy or prednisone before the biopsy. This
study has resulted in two manuscripts in preparation for peer reviewed
publications.
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CHF Grant # 1626
Significance of Tumour Suppressor Genes in Canine Cancer Principal Investigator: Jaime Modiano, VMD, PhD AMC Cancer Research Centre
Conclusions were that dogs with lymphoma and certain kinds of leukemia
express a receptor that is of interest in new approaches to treatment
of human hemolymphatic cancers. Therefore, research into developing
new targeted therapies for treatment of human cancers may possibly be
accomplished using dogs as a model of disease. This should benefit
dogs through the addition of human research money and effort toward
understanding canine lymphma and leukemia, and the potential
development of similar targeted treatments for canine cancers.
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CHF Grant # 2646
Characterization of Receptor Tyrosine Kinase Dysfunction in
Malignant Histiocytosis Principal Investigator: Cheryl London, DVM, PhD, University of
California, Davis
Malignant histiocytosis (MH), while rare in people, occurs frequently
in certain breeds of dogs including Rottweilers, Golden Retrievers,
Flat-Coated Retrievers and Bernese Mountain Dogs. There is no
effective therapy for this disease and nearly all patients die within
2 to 4 months of diagnosis. The purpose of this proposal is to
evaluate MH tumour specimens for mutations in genes that may
contribute to the development of this devastating cancer. The genes of
interest are those that code for proteins known as growth factor
receptors. These proteins are present on the surface of the cell and
when stimulated by growth factors, signal into the cell promoting cell
survival and growth. Dysregulation of growth factor receptors is a
common mechanism through which normal cells undergo transformation
into cancer cells. Significant research has been directed towards the
development of inhibitors capable of blocking the function of
dysregulated receptors. Recent success of this approach has been
realized with the inhibitor Gleevec in the treatment of chronic myelogenous leukemia in people.
The purpose of this proposal is to identify growth factor receptors
that are dysregulated in MH to provide the foundation for future
clinical application of growth factor receptor inhibitors in the
treatment of MH. The study commenced in October 2003, for a duration
of 2 years. Dogs are actively being recruited, who have been diagnosed
with malignant histiocytosis.
Rhonda Hovan, author of "Perspectives" articles for
The
Golden Retriever News Golden Retriever Club of America/Golden Retriever Foundation
Supported Canine Health Research Golden Retriever News; Vol. LV111, No. 6; November -
December 2001
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OVC prof takes
cancer research to new heights
OVC prof takes cancer research to new heights When Dr. Julius Liptak,
a recently-appointed assistant professor in small animal surgery
in OVC's Department of Clinical Studies, made the move from Colorado
to Guelph, the differences in elevation between the two areas
gave him some interesting food for thought. Now, with colleagues from
Colorado State University, he is embarking on the first study -
in veterinary or human medicine - to investigate the links between
rates of tumour growth and altitude. This study could lead to new
insights about how cancer progresses in people and animals. Liptak
explains that at higher altitudes, where there is less oxygen in the
air, the body responds by forming more blood vessels in order to
increase oxygen availability. Because of this, Liptak and his research
partners wonder if tumour growth may also be more aggressive at higher altitudes. This study,
funded by OVC's Pet Trust Fund, will investigate the effects of
altitude on tumour growth by comparing dogs afflicted with bone
tumours in Ontario with those in the Colorado Rockies. The study will
involve dogs that come to the OVC's Small Animal Clinic for treatment,
as well dogs who receive treatment at the Animal Cancer Center at
Colorado State University. Both groups of dogs will be treated with
the same chemotherapy drugs - the same medication used to treat cancer
in humans.
The outcomes of treatment and the rate of spread of the disease will
be compared. Liptak hopes that the study will benefit both dogs and
humans, and he says this is often the case with cancer research.
“Cancer's cancer,” he says. “The way it forms and spreads is the same
in dogs and people.” In a unique new study that will benefit both
humans an animals, Dr. Julius Liptak (at right with dog Eastwood) is
investigating the effects of altitude on tumour growth.
Typically, he says, studying cancer in dogs and cats can shed light on
human disease - in a fraction of the time it would take to study the
same thing in humans. “The biological behaviour of certain cancers is
the same in humans as it is in animals,” he says. “But, in dogs and
cats, cancer spreads more quickly because oftheir shorter life span.
This means that we can see a lot more quickly how successfu a
treatment will be.” As well, Liptak says that veterinary medicine can
gain from the expanse of knowledge and research about human cancer. In
a second project funded by Pet Trust, he is investigating the effects
of pre-operative chemotherapy - chemotherapy treatment before surgery
to remove cancerous growths - in dogs with bone tumours. “In humans,
there is a higher survival rate if chemotherapy is administered before
surgery,” he says. “We'll see if this is a case where something that
works for humans can also work for animals.” One might think that working with dogs
with cancer and their distressed owners would be emotionally draining, but Liptak says it's just the
opposite. “When owners come in, they know their dogs have cancer,” he
says. “So every day you can give them after treatment is another day
they might not otherwise have had.
It's very rewarding. The treatment of cancer is rarely a negative
experience. Many patients will eventually succumb to the disease, but
with the good quality of life provided by anticancer treatments, each
day is precious.”
- Karen Gallant
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ONGOING
RECRUITMENT OF CANINE TUMORS
For further
details on recruitment please contact
CVM_K9Genomics@ncsu.edu
Recruitment information Canine Soft Tissue Sarcomas
Recruitment information Canine lymphoma and osteosarcoma
Recruitment information Canine leukemia
Research
Focus:
Dr. Matthew Breen
graduated with honours in Genetics from the University
of Liverpool, U.K. in 1987. He completed his PhD,
working on cytogenetics of the Equidae in 1990. Dr.
Breen was employed as a Post Doctoral research scientist
in Molecular Genetics at the U.K. Medical Research
Council's Human Genetics Unit in Edinburgh, Scotland,
where he was responsible for developing improved
fluorescence in situ hybridization techniques as part of
the Human Genome Mapping Project. Dr. Breen then spent
four years working for the Australian Thoroughbred
industry, based at the University of Queensland,
Brisbane Australia. In 1996 Dr. Breen returned to the
U.K. where his laboratory developed molecular
cytogenetics reagents, resources and techniques for
application to canine and equine genome mapping,
comparative cytogenetics and cancer cancer studies. In
1998 Dr. Breen was awarded membership of the Institute
of Biology and the title of Chartered Biologist.In 2002
Dr. Breen relocated his laboratory to NCSU's College of
Veterinary Medicine as part of their Genomics
initiative. His research interests continue to focus on
genomics, genome mapping and the comparative aspects of
canine cancer.
CONTACT INFORMATION
FOR DR. MATTHEW BREEN
Matthew Breen PhD CBiol MIBiol
Associate Professor of Genomics
Dept. of Molecular Biomedical Sciences
College of Veterinary Medicine
North Carolina State University
CVM Research Building - Room 330 (lab), Room 348
(office)
4700 Hillsborough Street
Raleigh
North Carolina 27606
USA
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GOLDEN RETRIEVER CLUB OF AMERICA LYMPHOMA STUDY
The Vector Borne Disease Diagnostic Laboratory at the NCSU
College of Veterinary Medicine is recruiting cases for a
funded research project, which is investigating the
potential role of selected flea- and tick-borne bacteria as
co-factors in the development of lymphoma in Golden
Retrievers. This two-year study is being funded exclusively
by the Golden Retriever Foundation and the Canine Health
Foundation. The 1998 Golden Retriever Health Survey showed a
statistically significant decrease in lymphoma among Golden
Retrievers that had been treated with flea and tick
prevention products. This research project will examine one
mechanism by which these data might be explained - that
infection with Bartonella, Ehrlichia, and/or Anaplasma
species bacteria may predispose susceptible dogs to develop
lymphoma. The purpose of this study is to search for
evidence of Bartonella, Ehrlichia, and/or Anaplasma
infection in Golden Retriever dogs with lymphoma, as
compared to age- and sex-matched Golden Retrievers from the
same geographic region. Obtaining identical samples from
healthy control dogs will be critical to the scientific
evaluation of data obtained from Golden Retrievers with
lymphoma. Dr. Ed Breitschwerdt is the principal investigator
and Ashlee Duncan is the graduate student responsible for
the project.
The entry criteria for a case include: Golden Retrievers
with a new diagnosis of lymphoma that have not received any
antibiotics within 14 days prior to sample collection (or 30
days for azithromycin). Samples should be collected prior to
induction of chemotherapeutic agents.
The minimum entry criteria for a control include: Golden
Retrievers residing within 100 miles of the case dog and
lacking clinical evidence of lymphadenopathy, making the
possibility of undetected lymphoma unlikely. Additionally,
these control dogs must not have received any antibiotics
within 14 days prior to sample collection (or 30 days for
azithromycin). For each case, two to three control dogs will
be utilized. If possible, these healthy dogs should be
similar in age (± 18 months) and sex as the case dog.
Healthy dogs may be identified by the owner of the case dog,
selected by the case's attending veterinarian, or recruited
through the Golden Retriever Club of America. Cases and
controls recruited will receive free serological and
molecular testing for Bartonella, Ehrlichia, and Anaplasma
(a $360.00 value based on current serology/PCR testing costs
in our laboratory). Samples to be collected for this
research include whole blood, serum, lymph node aspirate(s),
and buccal swab(s).
Please contact us at 919-513-8279 or
awduncan@ncsu.edu for
further information.
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The Pet Fund
www.thepetfund.com
916-443-6007
The Pet Fund was founded in 2003 because there was at that time no
national nonprofit in the USA dedicated to funding veterinary care for
those who could not afford it. Animal shelter statistics across the
country demonstrated a constant increase in the number of animals
dropped off at shelters, many because of treatable medical conditions.
Thanks to the generousity of the law firm of O’Melveny & Myers, The Pet
Fund incorporated as a 501(c)3 and began raising funds to address this
growing problem. The staff and board members of The Pet Fund work
constantly to develop resources for pets and their families to fund
critically needed veterinary care, thus keeping animals out of shelters
and helping pet owners to become both financially independent and
skilled at preventative care practices. Since medical costs for animals
(as for people) are also on the rise, this is an ongoing funding
challenge. As a registered 501(c)3, all donations to The Pet Fund are
tax-deductible, and The Pet Fund strives to use the largest percentage
of donations possible for animal veterinary care above their operating
costs, which are minimal. Financial information is available upon
request from any interested donors, and they welcome questions about
their funding, application process, and development at
info@thepetfund.com.
(Please remember to put “The Pet Fund” in the subject
line of your e-mail.) |
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The National Childhood Cancer Foundation is leading the fight
against childhood cancer by supporting cooperative research at over
230 medical institutions in the United States. Members of this team,
the Children's Oncology Group, treat more than 90% of children with
cancer in North America. Together they develop new treatments much
more quickly and efficiently than if each worked alone. While almost
no child survived cancer in the 1950s, now over 70% can be cured.
However, more children still die of cancer than from any other
disease. The work of the National Childhood Cancer Foundation must
continue, until every child has a chance for a cure.
National Childhood Cancer Foundation
P.O. Box 60012
Arcadia CA 91066-6012
1-800-458-6223
www.nccf.org |
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http://www.petcard.ca/
With Petcard everyone can
afford the very best in pet
care. Petcard offers a
variety of ways you can
choose for your veterinary
services. You can choose to
finance the full amount, or
Petcard can finance a
portion. Your equal monthly
payments can also be
customized to suit your
budget; payment options
range from 6 months to 5
years.
Petcard is offered across
Canada for:
-
Veterinary
Treatments
-
Veterinary
Products
-
Pet
Purchases
-
Pet Food
-
Veterinary
Hospital
Stays
-
Veterinary
Dental Work
-
Pet
Vaccinations
-
Pet Grooming
-
Pet Boarding
Applying
for Petcard financing is
quite simple.
You complete a short
application form and fax it
to 1-888-689-9862.
You can also call Petcard
and they will take your
application information over
the phone.
Approval can be confirmed in
as little as 20 minutes.
Call 1-888-689-9876 if you
have any questions
-
No down
payment
-
No
collateral
-
High
Approval
-
Competitive
interest
rates
-
Monthly
payments
Remember . . .
-
Petcard
covers any
veterinary
or related
procedure or
product.
-
There is no
cost to you
for applying
for
financing or
to seek
approval.
-
Petcard
approval can
be given
almost
immediately,
even when
you are
right at
your
veterinary
clinic.
-
Petcard will
pay directly
to your
veterinary
service
provider.
You can
have a
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veterinary
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paid for,
and the full
amount. It
is up to
you.
-
It is up to
you, if you
would like
to pay a
deposit to
borrow.
-
If you go to
a
veterinarian
who is not
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with Petcard,
Petcard will
contact your
veterinarian,
inform them
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services
they
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then your
veterinarian
is given the
option to
register
with Petcard.
-
Petcard will
also
pre-approve
your
financing
BEFORE you
have chosen
a veterinary
service
provider.
-
Even if you
do not have
a credit
history, you
can have a
co-signer
whose credit
history
would
achieve an
approval,
and would be
willing to
assume
liability of
the loan.

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