A Phase II Study of JNJ-212082 (Abiraterone Acetate) in Metastatic Castration-Resistant Prostate Cancer Patients Who Have Received Docetaxel-based Chemotherapy
Overview
- Phase
- Phase 2
- Intervention
- Abiraterone
- Conditions
- Prostate Cancer
- Sponsor
- Janssen Research & Development, LLC
- Enrollment
- 47
- Primary Endpoint
- Percentage of Participants Achieving Prostate Specific Antigen (PSA) Response at Week 12
- Status
- Completed
- Last Updated
- 10 years ago
Overview
Brief Summary
The purpose of this study is to investigate the safety and efficacy of abiraterone in participants with metastatic castration-resistant prostate cancer (mCRPC) who have received docetaxel-based chemotherapy (treatment of disease, usually cancer, by chemical agents).
Detailed Description
This is a multi-center (conducted in more than one center), open-label (all people know the identity of the intervention), single-arm study to investigate safety and efficacy of abiraterone. The study consists of 3 phases: Screening phase (consists of 14 days before study commences on Day -1); Treatment phase (consists of 28-daily dosing cycles wherein abiraterone 1000 milligram \[mg\] once daily and 5 mg prednisolone twice daily will be given until disease progression or unacceptable toxicity is observed); and Follow-up phase (up to 5 years or until survival after the first dose of study drug). Abiraterone will be administered orally daily as at least 1 hour before the meal or 2 hours after the meal. Dose reduction will be allowed at the Investigator's discretion but not lower than 500 mg per day. Participants will discontinue study treatment at disease progression unless, in the Investigator's opinion, it is deemed that the participants will continue to derive benefit from abiraterone. Efficacy will be evaluated primarily through decline in prostate-specific antigen (substance in blood that is measured to check for prostate cancer) after 12 weeks of therapy. Participants' safety will be monitored throughout the study.
Investigators
Eligibility Criteria
Inclusion Criteria
- •In-patients or out-patients with histologically or cytologically confirmed adenocarcinoma of the prostate without neuroendocrine differentiation or small cell histology
- •Have surgically or medically castrated, with testosterone levels of less than 50 nanogram per deciliter
- •Have Prostate Specific Antigen (PSA) level of at least 5 nanogram per milliliter
- •Be under PSA progression according to Prostate-Specific Antigen Working Group (PSAWG) eligibility criteria or objective progression by Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.0 criteria for participants with measurable disease after androgen deprivation
- •Have been used at least 1 but not more than 2 cytotoxic chemotherapy regimens for Metastatic Castration-Resistant Prostate Cancer (mCRPC). At least 1 regimen must have contained docetaxel. If docetaxel-containing chemotherapy was used more than once, those of regimens containing docetaxel would be considered as 1 regimen in total
Exclusion Criteria
- •Has received other hormonal therapy, including any dose of finasteride, dutasteride, any herbal product known to decrease PSA levels or any systemic corticosteroid within 4 weeks prior to Cycle 1 Day 1 or has received ketoconazole for prostate cancer
- •Has received radiotherapy, chemotherapy (including estramustine) or immunotherapy (including provenge) within 4 weeks, or single fraction of palliative radiotherapy within 2 weeks prior to Cycle 1 Day 1
- •Has had surgery or local prostatic intervention within 4 weeks prior to Cycle 1 Day
- •In addition, any clinically relevant sequel from the surgery must have resolved prior to Cycle 1 Day 1
- •Has clinically significant heart disease as evidenced by myocardial infarction, or arterial thrombotic events, severe or unstable angina, or New York Heart Association (NYHA) Class 3 to 4 heart disease or cardiac ejection fraction measurement of less than 50 percent within 6 months prior to Cycle 1 Day 1
- •Has uncontrolled hypertension (systolic blood pressure greater than or equal to 160 millimeter of mercury or diastolic blood pressure greater than or equal to 95 millimeter of mercury)
Arms & Interventions
Abiraterone
Abiraterone 1000 milligram (mg) oral tablets will be administered once daily along with 5 mg oral prednisolone tablet administered twice daily for 28-daily dosing cycles and will be continued until disease progression or unacceptable toxicity.
Intervention: Abiraterone
Abiraterone
Abiraterone 1000 milligram (mg) oral tablets will be administered once daily along with 5 mg oral prednisolone tablet administered twice daily for 28-daily dosing cycles and will be continued until disease progression or unacceptable toxicity.
Intervention: Prednisolone
Outcomes
Primary Outcomes
Percentage of Participants Achieving Prostate Specific Antigen (PSA) Response at Week 12
Time Frame: Week 12
The PSA response will be evaluated according to Prostate-Specific Antigen Working Group (PSAWG) criterion, which is, greater than or equal to 50 percent decrease in PSA from Baseline up to 12 weeks after the first dose of study drug, which would be subsequently confirmed by a measurement that is at least 4 or more weeks after initial documentation of PSA.
Secondary Outcomes
- Duration of Prostate Specific Antigen (PSA) Response(Baseline and Day 1 of each cycle up to 5 years)
- Clinical Benefit(Baseline, Day 1 of Cycle 4, 7 and 10, and thereafter every third cycle up to 5 years)
- Decline in Serum Prostate Specific Antigen (PSA)(Baseline and Day 1 of each cycle up to 5 years)
- Overall Survival(Every 3 months until death or up to 5 years)
- Percentage of Participants With Radiographic Objective Response(Baseline, Day 1 of Cycle 4, 7 and 10, and thereafter every third cycle until first documented disease progression or up to 5 years)
- Percentage of Participants Achieving Prostate Specific Antigen (PSA) Response(Baseline and Day 1 of each cycle up to 5 years)
- Eastern Cooperative Oncology Group Performance Status (ECOG PS) Score(Baseline, Day 1, 8, 15 and 22 of Cycle 1 and 2, and thereafter Day 1 and 15 of all cycles up to 5 years)
- Radiographic Progression-Free Survival (RAD-PFS)(Baseline, Day 1 of Cycle 4, 7 and 10, and thereafter every third cycle until first documented disease progression, or up to 5 years)
- Prostate Specific Antigen Based Progression-Free Survival (PSA-PFS)(Baseline and Day 1 of each cycle until first documented disease progression or up to 5 years)
- Percentage of Participants With Circulating Tumor Cell (CTC) Conversion(Day 1 of Cycle 2, 3, and 4)