Goserelin, Flutamine, and Radiation Therapy in Treating Patients With Locally Advanced Prostate Cancer
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ClinicalTrials.gov Identifier: NCT00767286 |
Recruitment Status :
Completed
First Posted : October 7, 2008
Last Update Posted : January 28, 2014
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RATIONALE: Patient abstract not available
PURPOSE: Patient abstract not available
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Prostate Cancer | Drug: flutamide Drug: goserelin acetate Radiation: low-LET cobalt-60 gamma ray therapy Radiation: low-LET photon therapy | Phase 3 |
OBJECTIVES: I. Compare locoregional control, disease-free survival, and overall survival in patients with carcinoma of the prostate who are considered at high risk of relapse and receive long-term adjuvant zoladex (ZDX) vs. no adjuvant treatment following neoadjuvant ZDX/flutamide and radiotherapy. II. Compare sexual function in patients treated with these two regimens.
OUTLINE: Randomized study. Arm I: Neoadjuvant Antiandrogen Therapy and Releasing Factor Agonist Therapy plus Radiotherapy. Flutamide, FLUT, NSC-147834; and Zoladex, ZDX, NSC-606864; plus external-beam irradiation using megavoltage equipment with energies of at least 4 MV (at least 6 MV preferred). Arm II: Neoadjuvant Antiandrogen Therapy and Releasing Factor Agonist Therapy plus Radiotherapy followed by Adjuvant Releasing Factor Agonist Therapy. FLUT; and ZDX; plus external-beam irradiation using equipment as in Arm I; followed by ZDX.
PROJECTED ACCRUAL: 1,508 patients will be accrued over 2 years.
Study Type : | Interventional (Clinical Trial) |
Primary Purpose: | Treatment |
Official Title: | A PHASE III TRIAL OF THE USE OF LONG TERM TOTAL ANDROGEN SUPPRESSION FOLLOWING NEOADJUVANT HORMONAL CYTOREDUCTION AND RADIOTHERAPY IN LOCALLY ADVANCED CARCINOMA OF THE PROSTATE |
Actual Study Completion Date : | November 2003 |


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Ages Eligible for Study: | 50 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | Male |
Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS: Histologically confirmed, locally advanced adenocarcinoma of the prostate, including: Bulky primary tumors confined to the prostate (clinical Stage T2c) Primary tumors extending beyond the capsule (clinical Stage T3-4) No common iliac or para-aortic nodal involvement Regional lymph node involvement below the common iliac level allowed Positive nodes on imaging studies must be biopsied by FNA or surgical sampling PSA no more than 150 (mandatory) No distant metastases
PATIENT CHARACTERISTICS: Age: At least 50 Performance status: Karnofsky 70-100% Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified Other: No prior or concurrent second cancer except basal cell skin cancer No major medical or psychiatric illness that would prevent completion of treatment or interfere with follow-up
PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior chemotherapy Endocrine therapy: No prior hormonal therapy Radiotherapy: No prior radiotherapy Surgery: No prior radical surgery for carcinoma of the prostate

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00767286
Study Chair: | Gerald E. Hanks, MD | Fox Chase Cancer Center |
Other Publications:
ClinicalTrials.gov Identifier: | NCT00767286 |
Other Study ID Numbers: |
CDR0000077690 RTOG-9202 |
First Posted: | October 7, 2008 Key Record Dates |
Last Update Posted: | January 28, 2014 |
Last Verified: | July 2011 |
stage IIB prostate cancer stage IIA prostate cancer stage III prostate cancer stage IV prostate cancer |
Prostatic Neoplasms Genital Neoplasms, Male Urogenital Neoplasms Neoplasms by Site Neoplasms Prostatic Diseases Cobalt Goserelin Flutamide |
Antineoplastic Agents, Hormonal Antineoplastic Agents Trace Elements Micronutrients Physiological Effects of Drugs Androgen Antagonists Hormone Antagonists Hormones, Hormone Substitutes, and Hormone Antagonists |