Sirolimus Before Surgery in Treating Patients With Advanced Localized Prostate Cancer
- Conditions
- Prostate Cancer
- Interventions
- Registration Number
- NCT00311623
- Brief Summary
RATIONALE: Drugs used in chemotherapy, such as sirolimus, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.
PURPOSE: This clinical trial is studying the best dose of sirolimus and to see how well it works before surgery in treating patients with advanced localized prostate cancer.
- Detailed Description
OBJECTIVES:
Primary
* Determine the pharmacodynamically optimal dose (POD) of continuous daily oral sirolimus (rapamycin) in patients with advanced localized prostate cancer when given prior to radical prostatectomy, as measured by tumor S6 kinase inhibition by immunohistochemistry (IHC).
* Determine the proportion of men with downstream target inhibition in prostate tumor tissue at the POD using paired tumor biopsies from before and after rapamycin administration.
* Correlate tumor pharmacodynamic (PD) efficacy with a surrogate marker of tumor PD efficacy, peripheral blood mononuclear cell (PBMC) S6 kinase activity inhibition.
Secondary
* Characterize the serum and prostate tissue pharmacokinetics of daily oral rapamycin at 2 dose levels.
* Determine the relationship of PD target inhibition of S6 kinase activity with pretreatment Akt activity and PTEN loss by IHC in prostate cancer.
* Describe the relationship between PD inhibition with the mTOR inhibitor rapamycin and pretreatment prostate biopsy Gleason sum, Ki-67 index of proliferation, Akt activity, p27 IHC, and PTEN.
* Correlate PD efficacy as measured by downstream S6 kinase activity inhibition with markers of increased apoptosis (activated caspase 3) and reduction in markers of proliferation (change in Ki-67) in prostate tumor specimens.
* Quantify and characterize the toxicity of daily continuous rapamycin at 2 dose levels in generally healthy men with prostate cancer prior to surgery.
* Evaluate the activity of rapamycin in prostate cancer as measured in prostate specific antigen response prior to surgery.
OUTLINE: This is a multicenter, dose-escalation study.
Patients receive oral sirolimus (rapamycin) once daily on days 1-14 in the absence of unacceptable toxicity.
Cohorts of 12-21 patients receive escalating doses of rapamycin until the pharmacodynamically optimal dose is determined.
Patients undergo radical prostatectomy on day 15.
Patients undergo blood collection and tumor biopsies periodically during study for pharmacologic and correlative biomarker studies.
After completion of study treatment, patients are followed at 30 and 90 days.
PROJECTED ACCRUAL: A total of 42 patients will be accrued for this study.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 32
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description Low-dose Rapamycin (3mg) Rapamycin 3mg Men \>18years old with prostate cancer clinical stages T1c to T3, no metastases, Gleason sum of 7-10, multiple positive diagnostic cores, Eastern Cooperative Oncology Group (ECOG) performance status of 0-1, candidates for radical prostatectomy. Must have adequate hepatic, renal and bone marrow function, no allergy to rapamycins, avoid medications interfering with rapamycin metabolism, no active infection, no prior therapies for prostate cancer. Will receive rapamycin 3mg (Wyeth Pharmaceuticals, 1mg tablets) oral (PO) once daily on Days 1-14 with the last dose given on the morning before surgery (Day 15). High-dose Rapamycin (6mg) Rapamycin 6mg Men \>18years old with prostate cancer clinical stages T1c to T3, no metastases, Gleason sum of 7-10, multiple positive diagnostic cores, Eastern Cooperative Oncology Group (ECOG) performance status of 0-1, candidates for radical prostatectomy. Must have adequate hepatic, renal and bone marrow function, no allergy to rapamycins, avoid medications interfering with rapamycin metabolism, no active infection, no prior therapies for prostate cancer. Will receive rapamycin 6mg (Wyeth Pharmaceuticals, 2mg tablets) oral (PO) once daily on Days 1-14 with the last dose given on the morning before surgery (Day 15). Control group Radical prostatectomy Men \>18years old with prostate cancer clinical stages T1c to T3, no metastases, Gleason sum of 7-10, multiple positive diagnostic cores, Eastern Cooperative Oncology Group (ECOG) performance status of 0-1, candidates for radical prostatectomy. Receive no intervention on Days 1-14. Surgery performed on Day 15. Low-dose Rapamycin (3mg) Radical prostatectomy Men \>18years old with prostate cancer clinical stages T1c to T3, no metastases, Gleason sum of 7-10, multiple positive diagnostic cores, Eastern Cooperative Oncology Group (ECOG) performance status of 0-1, candidates for radical prostatectomy. Must have adequate hepatic, renal and bone marrow function, no allergy to rapamycins, avoid medications interfering with rapamycin metabolism, no active infection, no prior therapies for prostate cancer. Will receive rapamycin 3mg (Wyeth Pharmaceuticals, 1mg tablets) oral (PO) once daily on Days 1-14 with the last dose given on the morning before surgery (Day 15). High-dose Rapamycin (6mg) Radical prostatectomy Men \>18years old with prostate cancer clinical stages T1c to T3, no metastases, Gleason sum of 7-10, multiple positive diagnostic cores, Eastern Cooperative Oncology Group (ECOG) performance status of 0-1, candidates for radical prostatectomy. Must have adequate hepatic, renal and bone marrow function, no allergy to rapamycins, avoid medications interfering with rapamycin metabolism, no active infection, no prior therapies for prostate cancer. Will receive rapamycin 6mg (Wyeth Pharmaceuticals, 2mg tablets) oral (PO) once daily on Days 1-14 with the last dose given on the morning before surgery (Day 15).
- Primary Outcome Measures
Name Time Method Median S6 Kinase Inhibition in Prostate Tumor Tissue at the POD Change from baseline to 15 days post-intervention Pharmocodynamically Optimal Dose (POD) of Rapamycin as Determined by Number of Participants With Greater Than or Equal to 60% Tumor S6 Kinase Inhibition by Immunohistochemistry (IHC). Day 15 post-intervention Pharmacodynamic Response as Assessed by Median Post-treatment S6 Activity H-score Change from baseline to 15 days post-intervention Pharmocodynamic response was taken as ≥60% decrease in the H-score for S6 phosphorylation in the radical prostatectomy tumor tissue compared with the pretreatment (baseline) biopsy tumor tissue. The H-score is a semiquantitative measure of the percentage of cells scoring positive (0-100) multiplied by the intensity of staining (0-3).
- Secondary Outcome Measures
Name Time Method p27 as Measured by Immunohistochemistry (IHC) Change from baseline to 15 days post-intervention p27 by IHC in prostate cancer.
Pharmacokinetic Response of Rapamycin 6mg as Assessed by Whole Blood Analysis Change from baseline to 15 days post-intervention Snap-frozen prostate tissue was evaluated for tissue rapamycin levels.
Number of Participants With Change in Akt Phosphorylation as Measured by Immunohistochemistry (IHC) Change from baseline to 15 days post-intervention Number of participants with change (increased, decreased or no change) in Akt phosphorylation as measured by immunohistochemistry (IHC)
Reduction in Proliferation as Measured by Decrease in Ki-67 Baseline, 14 days post-intervention, 90-days post-operative Correlate PD efficacy as measured by downstream S6 kinase activity inhibition with markers of reduction in markers of proliferation (change in Ki-67) in prostate tumor specimens.
Toxicity as Per National Cancer Institute Common Toxicity Criteria v3.0 Baseline, 14 days post-intervention, 90-days post-operative Dose-limiting toxicity was defined as grade 3/4 neutropenia with fever lasting \>7 days, platelets of \<100,000/mm3 or associated with bleeding, grade ≥3 non-hematologic toxicity, or irreversible grade 2 toxicity related to rapamycine.
Pharmacokinetic Response of Rapamycin 3mg as Assessed by Whole Blood Analysis Change from baseline to 15 days post-intervention Snap-frozen prostate tissue was evaluated for tissue rapamycin levels.
PTEN Loss as Measured by Immunohistochemistry (IHC) Change from baseline to 15 days post-intervention Determine the relationship of PD target inhibition of S6 kinase activity with pretreatment PTEN loss by IHC in prostate cancer.
Increased Apoptosis as Measured by Activated Caspase 3 Baseline, 14 days post-intervention, 90-days post-operative Correlate PD efficacy as measured by downstream S6 kinase activity inhibition with markers of increased apoptosis (activated caspase 3) in prostate tumor specimens.
Change in Gleason Sum Change from baseline to 15 days post-intervention pretreatment biopsy compared to post-treatment radical prostatectomy specimen
Activity of Rapamycin as Measured by Prostate Specific Antigen (PSA) Response Prior to Surgery Change from baseline to Day 14 PSA response to daily rapamycin
Trial Locations
- Locations (3)
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
🇺🇸Baltimore, Maryland, United States
University of Michigan Comprehensive Cancer Center
🇺🇸Ann Arbor, Michigan, United States
Duke Comprehensive Cancer Center
🇺🇸Durham, North Carolina, United States