Androgen Suppression and Radiation With/Out Docetaxel in High-Risk Localized Prostate Cancer
- Conditions
- Prostate Cancer
- Interventions
- Procedure: neoadjuvant therapyProcedure: quality-of-life assessmentRadiation: radiation therapy
- Registration Number
- NCT00651326
- Lead Sponsor
- NCIC Clinical Trials Group
- Brief Summary
RATIONALE: Androgens can cause the growth of prostate cancer cells. Antihormone therapy, such as flutamide, bicalutamide, leuprolide, buserelin, and goserelin, may lessen the amount of androgens made by the body. Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. It is not yet known whether giving androgen suppression therapy together with radiation therapy is more effective with or without docetaxel in treating prostate cancer.
PURPOSE: This randomized phase III trial is studying androgen suppression therapy, radiation therapy, and docetaxel to see how well they work compared with androgen suppression therapy and radiation therapy in treating patients with high-risk localized prostate cancer.
CLOSURE: This trial closed to further accrual in November 2009. The study endpoints will not be reached.
- Detailed Description
OBJECTIVES:
Primary
* To compare disease-free survival rates in patients with high-risk localized adenocarcinoma of the prostate treated with androgen suppression therapy and radiotherapy with vs without docetaxel.
Secondary
* To compare overall survival.
* To compare time to biochemical disease progression.
* To compare time to local disease progression.
* To compare time to distant disease progression.
* To compare time to next anticancer therapy.
* To compare progression-free survival.
* To compare degree of prostate-specific antigen (PSA) suppression prior to radiotherapy.
* To compare quality of life (QOL) using EORTC QLQ C30 and EORTC QLQ PR25 questionnaires and a trial-specific checklist.
* To compare the nature, severity, and frequency of adverse events.
OUTLINE: This is a multicenter study. Patients are stratified according to Gleason score (≤ 7 vs ≥ 8), baseline prostate-specific antigen (PSA) (\> 20 ng/mL vs ≤ 20 ng/mL), and participating center. Patients are randomized to 1 of 2 treatment arms.
* Arm I: Patients receive androgen suppression therapy comprising oral flutamide three times daily or oral bicalutamide once daily for 4 weeks AND leuprolide subcutaneously (SC) or intramuscularly every 1-6 months, buserelin SC every 2 or 3 months, or goserelin SC every 1 or 3 months for 3 years. Patients also receive docetaxel IV over 60 minutes on day 1. Treatment with docetaxel repeats every 21 days for up to 4 courses. Beginning at least 4 weeks after completion of chemotherapy, patients undergo pelvic radiotherapy once daily 5 days a week for up to 8 weeks.
* Arm II: Patients receive androgen suppression therapy and undergo pelvic radiotherapy as in arm I.
Patients complete quality of life questionnaires at baseline, periodically during treatment, and then every 6 months for 5 years.
After completion of study treatment, patients are followed at 3 and 6 months, every 6 months for 5 years, and then annually thereafter.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Male
- Target Recruitment
- 48
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Antiandrogen; LHRH; Radiation Therapy leuprolide acetate Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Antiandrogen; LHRH; Radiation Therapy neoadjuvant therapy Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Antiandrogen; LHRH; Docetaxel, Radiation Therapy neoadjuvant therapy Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel Antiandrogen; LHRH; Docetaxel, Radiation Therapy radiation therapy Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel Antiandrogen; LHRH; Docetaxel, Radiation Therapy leuprolide acetate Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel Antiandrogen; LHRH; Docetaxel, Radiation Therapy quality-of-life assessment Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel Antiandrogen; LHRH; Radiation Therapy quality-of-life assessment Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Antiandrogen; LHRH; Radiation Therapy radiation therapy Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Antiandrogen; LHRH; Docetaxel, Radiation Therapy bicalutamide Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel Antiandrogen; LHRH; Docetaxel, Radiation Therapy goserelin Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel Antiandrogen; LHRH; Docetaxel, Radiation Therapy flutamide Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel Antiandrogen; LHRH; Docetaxel, Radiation Therapy Docetaxel Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel Antiandrogen; LHRH; Radiation Therapy bicalutamide Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Antiandrogen; LHRH; Radiation Therapy flutamide Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Antiandrogen; LHRH; Radiation Therapy buserelin Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Antiandrogen; LHRH; Radiation Therapy goserelin Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Antiandrogen; LHRH; Docetaxel, Radiation Therapy buserelin Antiandrogen (Flutamide or Bicalutamide) LHRH agonist (Eligard) Docetaxel
- Primary Outcome Measures
Name Time Method Disease-free survival
- Secondary Outcome Measures
Name Time Method Overall survival Time to distant disease progression Progression-free survival Quality of life Time to local disease progression Time to biochemical disease progression Time to next anti-cancer therapy Degree of prostate-specific antigen (PSA) suppression prior to radiotherapy Adverse events
Trial Locations
- Locations (13)
McGill University - Dept. Oncology
🇨🇦Montreal, Canada
Tom Baker Cancer Centre
🇨🇦Calgary, Canada
Juravinski Cancer Centre at Hamilton Health Sciences
🇨🇦Hamilton, Canada
BCCA - Cancer Centre for the Southern Interior
🇨🇦Kelowna, Canada
Cross Cancer Institute
🇨🇦Edmonton, Canada
London Regional Cancer Program
🇨🇦London, Canada
Credit Valley Hospital
🇨🇦Mississauga, Canada
Lakeridge Health Oshawa
🇨🇦Oshawa, Canada
Saskatoon Cancer Centre
🇨🇦Saskatoon, Canada
Ottawa Health Research Institute - General Division
🇨🇦Ottawa, Canada
Univ. Health Network-Princess Margaret Hospital
🇨🇦Toronto, Canada
BCCA - Vancouver Cancer Centre
🇨🇦Vancouver, Canada
CancerCare Manitoba
🇨🇦Winnipeg, Canada