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Prostate Cancer Vaccine Trial
Untitled Document
Name of the Trial
Phase I Pilot Study of Vaccine Therapy Comprising Priming Vaccinations of Vaccinia-PSA-TRICOM
and Recombinant Fowlpox GM-CSF (rF-GM-CSF) Followed By Boosting Vaccinations
of Fowlpox-PSA-TRICOM With or Without rF-GM-CSF in Patients With Progressive
or Locally Recurrent Prostate Cancer (NCI-05-C-0017). See the protocol
summary.
Principal Investigator
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Dr. James Gulley
Principal Investigator |
Dr. James Gulley, NCI Center for Cancer Research.
Why This Trial Is Important
Excluding non-melanoma skin cancers, prostate cancer is the most common cancer
- and the third most deadly - among North American men. Despite advances in
early detection and treatment, the disease recurs in 30 to 40 percent of patients.
Although several treatment options exist for recurrent disease, there is no
consensus on which is best and additional treatment options are needed.
Prostate-specific antigen (PSA), a protein made by the prostate gland, is often
overproduced in prostate cancer. Several studies have shown that PSA-containing
vaccines can stimulate the immune system to produce T lymphocytes capable of
killing prostate cancer cells. Moreover, some studies in mice suggest that injecting
vaccines directly into tumors dramatically boosts the immune response, killing
more tumor cells.
In this study, researchers are testing this approach in patients with prostate
cancer that has recurred locally or progressed following previous treatment.
Besides PSA, the vaccines they are using contain T-cell costimulatory molecules
to further boost the body's immune response.
"We believe that by placing the vaccine directly into the tumor, the resulting
increase in local immune activation will be like shining a laser on the tumor,
making it a better target for the T cells," says Dr. Gulley.
Who Can Join This Trial
Researchers seek to enroll up to 30 men aged 18 or over with prostate cancer
that has recurred locally after previous radiotherapy or cryotherapy or has
progressed despite androgen deprivation therapy. See the list
of eligibility criteria.
Study Site and Contact Information
This study is taking place at the NIH Clinical Center in Bethesda, Md. For
more information, call the NCI Clinical Studies Support Center (CSSC) toll free
at 1-888-NCI-1937. The call is confidential.
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