Clinical Trials Directory

Trials / Terminated

TerminatedNCT00949962

Post-operative or Early Salvage XRT and ADT for High Risk PCa

Immediate or Early Salvage Post-operative External Radiotherapy Combined With Concomitant and Adjuvant Hormonal Treatment Versus Immediate or Early Salvage Postoperative External Radiotherapy Alone in pT3a-b R0-1 cN0M0 / pT2R1 cN0M0, Gleason Score 5-10 Prostatic Carcinoma. A Phase III Study

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
87 (actual)
Sponsor
European Organisation for Research and Treatment of Cancer - EORTC · Network
Sex
Male
Age
80 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Conformal radiation therapy uses a 3-dimensional (3-D) image of the tumor to help focus thin beams of radiation directly on the tumor. Giving conformal external-beam radiation therapy in higher doses over a shorter period of time may kill more tumor cells and have fewer side effects. Androgens can cause the growth of prostate cancer cells. Hormone therapy, such as leuprolide acetate, may lessen the amount of androgens made by the body. It is not yet known whether radiation therapy is more effective when given together with or without hormone therapy in treating patients with prostate cancer who have undergone surgery. PURPOSE: This randomized phase III trial is studying radiation therapy to see how well it works compared with radiation therapy given together with hormone therapy in treating patients who have undergone surgery for stage I, stage II, or stage III prostate cancer.

Detailed description

OBJECTIVES: * To investigate the potential benefit of post-operative radiotherapy with vs without a combined and adjuvant treatment consisting of short-term androgen suppression for improving the biochemical progression-free survival of patients who have undergone radical prostatectomy for stage I-III prostate cancer. OUTLINE: This is a multicenter study. Patients are stratified according to institution, pathological stage (pT2R1 vs pT3R0 vs pT3R1), Gleason sum (≤ 3+4 vs ≥ 4+3), and WHO performance status (0 vs 1). Within 3 months after radical surgery, patients are randomized to 1 of 2 treatment arms. * Arm I: Patients undergo post-operative conformal external beam irradiation for 6.5 weeks. * Arm II: Beginning between days -5 to -3, patients receive an antiandrogen for 2-4 weeks. Beginning on day 0, patients receive leuprolide acetate subcutaneously once (6-month depot) and undergo conformal external beam irradiation 5 times weekly for 6.5 weeks. Patients undergo quality of life assessments periodically. After completion of study treatment, patients are followed up every 6 months for 5 years and then yearly thereafter.

Conditions

Interventions

TypeNameDescription
DRUGantiandrogen therapyGiven systemically
DRUGleuprolide acetateGiven subcutaneously
RADIATION3-dimensional conformal radiation therapyUndergo radiotherapy

Timeline

Start date
2009-10-01
Primary completion
2015-12-01
Completion
2016-06-01
First posted
2009-07-31
Last updated
2014-07-04

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT00949962. Inclusion in this directory is not an endorsement.