4.7 Article Proceedings Paper

Phase III trial of long-term adjuvant androgen deprivation after neoadjuvant hormonal cytoreduction and radiotherapy in locally advanced carcinoma of the prostate: The Radiation Therapy Oncology Group Protocol 92-02

Journal

JOURNAL OF CLINICAL ONCOLOGY
Volume 21, Issue 21, Pages 3972-3978

Publisher

AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.2003.11.023

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Funding

  1. NATIONAL CANCER INSTITUTE [U10CA021661, U10CA032115] Funding Source: NIH RePORTER
  2. NCI NIH HHS [CA-21661, CA-32115] Funding Source: Medline

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(Purpose) under bar: Radiation Therapy Ontology Group (RTOG) Protocol 92-02 was a randomized trial testing long-term (LT) adjuvant androgen deprivation (AD) after initial AD with external-beam radiotherapy (RT) in patients with locally advanced prostate cancer (PC; T2c-4) and with prostate-specific antigen level less than 150 ng/mL. (Patients and Methods) under bar: Patients received a total of 4 months of goserelin and flutamide, 2 months before and 2 months during FIT. A radiation dose of 65 to 70 Gy was given to the prostate and a dose of 44 to 50 Gy to the pelvic lymph nodes. Patients were randomly assigned to receive no additional therapy (short-term [ST]AD-RT) or 24 months of goserelin (LTAD-RT),- 1,554 patients were entered onto the study. (Results) under bar: The LTAD-RT arm showed significant improvement in all efficacy end points except overall survival (OS, 80.0% v 78.5% at 5 years, P = .73), compared with the STAD-RT arm. In a subset of patients not part of the original study design, with tumors assigned Gleason scares of 8 to 10 by the contributing institutions, the LTAD-RT arm had significantly better OS (81.0% v 70.7%, P = .044). There was a small but significant increase in the frequency of late radiation grades 3, 4, and 5 gastrointestinal toxicity ascribed to the LTAD-RT arm (2.6% v 1.2% at 5 years, P = .037), the cause of which is not clear. (Conclusion) under bar: The RTOG 92-02 trial supports the addition of LT adjuvant AD to STAD with RT for T2c-4 PC. In the exploratory subset analysis of patients with Gleason scares 8 to 10, LT adjuvant AD resulted in a survival advantage. (C) 2003 by American Society of Clinical Oncology.

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