RATIONALE: Androgens can cause the growth of prostate cancer cells. Drugs, such as triptorelin and flutamide, may stop the adrenal glands from making androgens. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving triptorelin and flutamide together with radiation therapy may be an effective treatment for prostate cancer. It is not yet known whether giving triptorelin and flutamide together with external-beam radiation therapy is more effective than external-beam radiation therapy alone in treating prostate cancer. PURPOSE: This randomized phase III trial is studying triptorelin, flutamide, and external-beam radiation therapy to see how well they work compared to external-beam radiation therapy alone in treating patients with stage II or stage III prostate cancer.
OBJECTIVES: * Compare the impact of neoadjuvant androgen blockade therapy comprising triptorelin and flutamide followed by conformal external beam radiotherapy and continued androgen blockage therapy vs conformal external beam radiotherapy alone in patients with stage II or III prostate cancer. * Compare the survival rate, in terms of 5-year clinical or biological remission, in patients treated with these regimens. * Compare overall survival in patients treated with these regimens. * Compare acute and late toxicity of these regimens in these patients. * Compare quality of life of patients treated with these regimens. * Determine the value and time-delay to obtain prostate-specific antigen nadir in patients treated with external beam radiotherapy alone. OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients undergo conformal external beam radiotherapy. * Arm II: Patients receive androgen blockade therapy comprising triptorelin subcutaneously every 4 weeks and oral flutamide once daily. Androgen blockade therapy continues for a total of 4 months. Two months after initiation of androgen blockade therapy, patients undergo conformal external beam radiotherapy. Quality of life is assessed. PROJECTED ACCRUAL: A total of 450 patients will be accrued for this study.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
378
Clinique De Rochebelle
Alès, France
Institut Sainte Catherine
Avignon, France
Hopital Louis Pasteur
Colmar, France
Hopitaux Civils de Colmar
Colmar, France
Centre Hospitalier Universitaire Henri Mondor
Créteil, France
Hopital Intercommunal De Creteil
Créteil, France
Hopital Jean Monnet
Épinal, France
Centre Hospitalier Intercommunal des Alpes du Sud
Gap, France
Centre Oscar Lambret
Lille, France
Centre Hospital Regional Universitaire de Limoges
Limoges, France
...and 21 more locations
Impact of complete androgen blockade for 4 months
Survival, in terms of clinical or biological remission, at 5 years
Overall survival
Acute and late toxicity
Quality of life
Value and time-delay to obtain prostate-specific antigen nadir (for patients undergoing external beam radiotherapy alone)
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