Vaccine Therapy With PROSTVAC/TRICOM and Flutamide Versus Flutamide Alone to Treat Prostate Cancer
Prostate Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00450463 ↗Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Sargramostim (GM-CSF, Leukine) (Drug); Flutamide (Eulexin) (Drug); PROSTVAC-F/ TRICOM (Biological); PROSTVAC-V/TRICOM (Biological)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Male
- Sponsor
- National Cancer Institute (NCI)
- Primary completion
- Apr 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Time to Treatment Failure |
4.5; 6.9 | — |
| SECONDARY Count of Participants With Serious and Non-serious Adverse Events Assessed by the Common Terminology Criteria in Adverse Events (CTCAE v4.0) |
33; 31; 11 | — |
| SECONDARY Number of Participants With Prostatic Specific Antigen (PSA) Response |
7; 7 | — |
| SECONDARY Percentage of Participants With Antigen Specific Immune Responses Against Prostatic Specific Antigen (PSA) |
58; 56 | — |
Summary
Eligibility Criteria
- INCLUSION CRITERIA:
A. Histopathological documentation of prostate cancer confirmed in the Laboratory of Pathology at the: National Institutes of Health (NIH) Clinical Center prior to starting this study. If no pathologic specimen is available, patients may enroll with a pathologists report showing a histologic diagnosis of prostate cancer and a clinical course consistent with the disease.
B. Must have non-metastatic androgen insensitive prostate cancer with a rising PSA (prostatic specific antigen) with castrate levels of testosterone and no evidence of metastatic disease on CT (computed tomography) scan or bone scan. A rising PSA is defined as two consecutively rising PSA levels, separated by at least 1 month apart, with the last measurement that is greater than 1ng/ml. Patients on nilutamide therapy must undergo nilutamide withdrawal for at least 4 weeks and still show evidence of a rising PSA. Following treatment with bicalutamide, patients must undergo withdrawal for at least 6 weeks and still show evidence of a rising PSA.
C. Life expectancy greater than or equal to 6 months.
D. ECOG (Eastern Cooperative Oncology Group) 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 to 1,500/mm(3).
- Platelet count greater than or equal to 100,000/mm(3)
- Hgb (Hemoglobin) 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 patients with Gilbert's syndrome, a total bilirubin less than or equal to 3.0 mg/dL, AST (aspartate aminotransferase) and ALT (alanine aminotransferase) less than 2.5 times upper limit of normal
H. No other active malignancies within the past 3 years (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. Able to understand and sign informed consent.
L. Must agree to use effective birth control (such as a condom) or abstinence during and for a period of 4 months after the last vaccination therapy. Patients must be willing to remain on chemical castration therapy, unless they have had surgical castration.
M. Patients must have recovered from acute toxicities related to prior therapy or surgery.
N. Parameters for assessment of baseline renal function:
Serum creatinine less than or equal to 1.5 times the upper limit of normal OR creatinine clearance on a 24-h urine collection of greater than or equal to 60 mL/min.
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.
- Concurrent use of topical steroids (including steroid eye drops) or systemic steroids. Nasal or inhaled steroid use is permitted.
- Patients who have undergone allogenic peripheral stem cell transplantation or solid organ transplantation requiring immunosuppression.
B. Patients who test positive for active Hepatitis B or Hepatitis C infection.
C. 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, myasthenia gravis, Goodpasture syndrome, active Grave's disease.
D. History of allergy or untoward reaction to prior vaccination with vaccinia virus or to any component of the vaccinia vaccine regimen.
E. 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: person
Data sourced from ClinicalTrials.gov (NCT00450463). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.