Status:
COMPLETED
Vaccine and Antibody Treatment of Prostate Cancer
Lead Sponsor:
National Cancer Institute (NCI)
Conditions:
Prostatic Neoplasms
Eligibility:
MALE
18-85 years
Phase:
PHASE1
Brief Summary
This study will evaluate the side effects of a fixed dose of vaccine and GM-CSF with increasing doses of anti-CTLA-4 antibody in patients with advanced prostate cancer. The vaccine consists of a "prim...
Detailed Description
Background: * Adenocarcinoma of the prostate is the most common cancer diagnosis in American males, and the second leading cause of cancer death. * The proposed vaccine strategy represents a third-ge...
Eligibility Criteria
Inclusion
- INCLUSION CRITERIA:
- A. Histopathological documentation of prostate cancer confirmed in the Laboratory of Pathology at the: NIH Clinical Center, National Institutes of Health (NIH), the National Naval Medical Center, or Walter Reed Army Medical Center prior to starting this study. If no pathologic specimen is available, patients may enroll with a pathologist's report showing a histologic diagnosis of prostate cancer and a clinical course consistent with the disease.
- B. Must have metastatic androgen insensitive prostate cancer with no bone pain requiring narcotics and have had no prior chemotherapy.
- C. Life expectancy greater than or equal to 6 months.
- D. ECOG performance status of 0-1.
- E. No systemic steroid or steroid eye drop use within 2 weeks prior to initiation of experimental therapy.
- F. Hematological eligibility parameters
- Granulocyte count greater than or equal to1,500/mm(3)
- Platelet count greater than or equal to100,000/mm(3)
- Hgb greater than or equal to 9 Gm/dL
- Lymphocyte count greater than or equal to 500/mm(3).
- G. Biochemical eligibility parameters (within 16 days of starting therapy)
- Hepatic function: Bilirubin less than or equal to 1.5 mg/dl (OR in patients with Gilbert's syndrome, a total bilirubin less than or equal to 3.0 mg/dL), AST and ALT less than or equal to 2.5 times upper limit of normal
- H. No other active malignancies within the past 12 months (with the exception of non-melanoma skin cancers or carcinoma in situ of the bladder) or life threatening illnesses.
- I. Willing to travel to the NIH for follow-up visits.
- J. 18 years of age or greater.
- K. Vaccinia-naive or vaccinia immune.
- L. Able to understand and sign informed consent.
- M. Agree to use adequate contraception prior to study entry and for at least 4 months following the last vaccine injection.
- N. Patients must remain on medical castration therapy, unless they have had surgical castration
- O. Patients must have recovered from acute toxicities related to prior therapy or surgery. For chemotherapy typically this is 3-4 weeks.
- P. Parameters for assessment of baseline renal function:
- Serum creatinine not above the institution limits of normal, OR creatinine clearance on a 24 hour urine collection of greater than or equal to 60 mL/min.
- Patients must have less than grade 2 proteinuria (unless the cause is determined not to be renal.)
- EXCLUSION CRITERIA:
- A. Patients should have no evidence of being immunocompromised as listed below.
- Human immunodeficiency virus positivity due to the potential for decreased tolerance and may be at risk for severe side effects.
- Hepatitis B or C positivity
- Concurrent use of topical steroids (including steroid eye drops) or systemic steroids. Nasal or inhaled steroid use is permitted
- B.Patients should have no autoimmune diseases that have required treatment such as, Addison's disease, Hashimoto's thyroiditis, or systemic lupus erythematous, Sjogren syndrome, scleroderma, Goodpasture syndrome, and active Grave's disease. Also excluded are patients with autoimmune hemolytic anemia, ulcerative and hemorrhagic colitis, endocrine disorders (e.g., thyroiditis, hyperthyroidism, hypothyroidism, autoimmune hypophysitis/hypopituitarism, and adrenal insufficiency), sarcoid granuloma, myasthenia gravis, polymyositis, and Guillain-Barre syndrome. Patients with a history of autoimmunity that has not required systemic immunosuppressive therapy or does not threaten vital organ function including CNS, heart, lungs, kidneys, skin, and GI tract will be allowed.
- C. History of allergy or untoward reaction to prior vaccination with vaccinia virus or to any component of the vaccinia vaccine regimen.
- D. Do not administer the recombinant vaccinia vaccine if the recipient, or for at least three weeks after vaccination, their close household contacts (close household contacts are those who share housing or have close physical contact) are: persons with active or a history of eczema or other eczematoid skin disorders; those with other acute, chronic or exfoliative skin conditions (e.g., atopic dermatitis, burns, impetigo, varicella zoster, severe acne, or other open rashes or wounds) until condition resolves; pregnant or nursing women; children 3 years of age and under; and immunodeficient or immunosuppressed persons (by disease or therapy), including HIV infection.
- E. Serious intercurrent medical illness (e.g., one that requires treatment) which would interfere with the ability of the patient to carry out the treatment program, including, but not limited to, inflammatory bowel disease, Crohn's disease, ulcerative colitis, or active diverticulitis.
- F. Patients with cardiac disease that have fatigue, palpitation, dyspnea or angina with ordinary physical activity (New York Heart Association class 2 or greater) are not eligible.
- G. Patients with a history of congestive heart failure or who have objective evidence of congestive heart failure by physical exam or imaging are not eligible.
- H. Patients with pulmonary disease that have fatigue or dyspnea with ordinary physical activity are not eligible.
- I. Concurrent chemotherapy.
- J. No brain metastasis, or with a history of seizures, encephalitis, or multiple sclerosis.
- K. Serious hypersensitivity reaction to egg products.
- L. Prior splenectomy.
- M. Patients who have received prior MDX-01.
Exclusion
Key Trial Info
Start Date :
June 8 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2011
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT00113984
Start Date
June 8 2005
End Date
December 1 2011
Last Update
December 16 2019
Active Locations (1)
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1
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States, 20892