Phase III Study Comparing Irradiation at a Dose of 80 Gy to Irradiation at 70 Gy in Unfavorable Prostate Cancers Associated With Prolonged Hormonal Therapy
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Prostate Cancer
- Sponsor
- UNICANCER
- Enrollment
- 500
- Locations
- 25
- Primary Endpoint
- Biochemical or clinical progression-free survival at 5 years
- Status
- Active, not recruiting
- Last Updated
- last year
Overview
Brief Summary
RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. It is not yet known which dose of radiation therapy is more effective in treating patients with prostate cancer.
PURPOSE: This randomized phase III trial is comparing two radiation therapy regimens in treating patients with prostate cancer receiving hormone therapy.
Detailed Description
OBJECTIVES: Primary * Assess the impact of increasing the radiation dose 10 Gy on biochemical or clinical progression-free survival at 5 years in patients with unfavorable-risk prostate cancer receiving prolonged hormone therapy. Secondary * Evaluate overall and specific survival. * Assess acute and late toxicities of different modalities (conformal or intensity-modulated radiotherapy). * Evaluate toxicities of the different doses with respect to hormonal therapy. * Assess the quality of life (QLQ-C30 and PR 25). OUTLINE: This is a multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients undergo 80 Gy of conformal or intensity-modulated radiotherapy 5 times a week for 7-8 weeks. * Arm II: Patients undergo 70 Gy of conformal or intensity-modulated radiotherapy 5 times a week for 7-8 weeks. In both arms, patients receive goserelin subcutaneously once every 3 months for up to 3 years. After completion of study treatment, patients are followed up periodically for 10 years.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
Biochemical or clinical progression-free survival at 5 years
Time Frame: 5 years
Secondary Outcomes
- Acute and late toxicity(10 years)
- Quality of life as measured by QLQ-C30 and PR 25 questionnaires(10 years)
- Overall and specific survival(10 years)