Prospective Phase II Study Evaluating the Feasibility of a Conformational Pelvic and Prostatic Radiotherapy With Simultaneous Integrated Boost Modulated-intensity Arctherapy (SIB-IMAT) in Combination With Long Term Androgen Deprivation for High Risk Localized Prostate Cancer.

Date de début de l'étude : 1 octobre 2012

Inclusion Criteria: Histologically confirmed adenocarcinoma of the prostate High risk localized adenocarcinoma defined by at least one of the following criteria: Clinical stage T2c, T3 or T4 Gleason score ≥ 8 Prostate-specific antigen (PSA)≥ 20 ng/ml and ≤ 100 ng/ml Patient cN0, pN0 or Nx (negative lymphadenectomy or no lymphadenectomy) No pelvic adenopathy ≥ 15 mm on CT or MRI, Absence of bone and/or visceral metastasis Androgen deprivation beginning no later than the day of radiotherapy and up to six months before irradiation Absence of prior pelvic radiotherapy, Absence of surgical treatment of prostate cancer except transurethral resection performed within 4 months minimum before radiotherapy, Age ≥ 18 years and ≤ 85 years ECOG performance status ≤ 1, Estimated life expectancy > 5 years Membership of a social security system, Signed informed consent. Exclusion Criteria: Prostate cancer histology other than adenocarcinoma, pN1 patients (lymph node dissection after histologically proven) PSA > 100 ng/ml History of cancer within 5 years prior to trial entry (with the exception of basal cell carcinoma skin) Patient with severe hypertension uncontrolled by appropriate treatment (≥ 160 mm Hg systolic and / or ≥ 90 mm Hg diastolic) Contra-indication for pelvic irradiation (eg scleroderma, chronic inflammatory disease of the digestive tract, etc ...) Contra-indication to agonists or antagonists of LH-RH Bilateral hip prosthesis, Patients already included in another clinical trial with an experimental molecule, Persons deprived of liberty or under guardianship Unable to undergo medical test for geographical, social or psychological.