Published June 1, 2017 | Version v1
Journal article

Duration of Androgen Deprivation in Locally Advanced Prostate Cancer: Long-Term Update of NRG Oncology RTOG 9202

  • 1. Medical College of Wisconsin, Milwaukee, Wisconsin (United States)
  • 2. University of Chicago, Chicago, Illinois (United States)
  • 3. Fox Chase Cancer Center, Philadelphia, Pennsylvania (United States)
  • 4. New York University, New York, New York (United States)
  • 5. Indiana University, Indianapolis, Indiana (United States)
  • 6. Northeast Radiation Oncology Center, Dunmore, Pennsylvania (United States)
  • 7. Sutter General Hospital, Sacramento, California (United States)
  • 8. Albert Einstein Medical Center, Philadelphia, Pennsylvania (United States)
  • 9. London Regional Cancer Program, London, Ontario (Canada)
  • 10. Mayo Clinic, Rochester, Minnesota (United States)
  • 11. Wayne State University-Karmanos Cancer Institute, Detroit, Michigan (United States)
  • 12. Cross Cancer Institute, Edmonton, Alberta (Canada)
  • 13. University of Colorado Denver, Denver, Colorado (United States)
  • 14. University of California, San Francisco, California (United States)
  • 15. University of Maryland Medical System, Baltimore, Maryland (United States)
  • 16. NRG Oncology Statistics and Data Management Center, Philadelphia, Pennsylvania (United States)
  • 17. Cedars-Sinai Medical Center, Los Angeles, California (United States)

Description

Purpose: Trial RTOG 9202 was a phase 3 randomized trial designed to determine the optimal duration of androgen deprivation therapy (ADT) when combined with definitive radiation therapy (RT) in the treatment of locally advanced nonmetastatic adenocarcinoma of the prostate. Long-term follow-up results of this study now available are relevant to the management of this disease. Methods and Materials: Men (N=1554) with adenocarcinoma of the prostate (cT2c-T4, N0-Nx) with a prostate-specific antigen (PSA) <150 ng/mL and no evidence of distant metastasis were randomized (June 1992 to April 1995) to short-term ADT (STAD: 4 months of flutamide 250 mg 3 times per day and goserelin 3.6 mg per month) and definitive RT versus long-term ADT (LTAD: STAD with definitive RT plus an additional 24 months of monthly goserelin). Results: Among 1520 protocol-eligible and evaluable patients, the median follow-up time for this analysis was 19.6 years. In analysis adjusted for prognostic covariates, LTAD improved disease-free survival (29% relative reduction in failure rate, P<.0001), local progression (46% relative reduction, P=.02), distant metastases (36% relative reduction, P<.0001), disease-specific survival (30% relative reduction, P=.003), and overall survival (12% relative reduction, P=.03). Other-cause mortality (non–prostate cancer) did not differ (5% relative reduction, P=.48). Conclusions: LTAD and RT is superior to STAD and RT for the treatment of locally advanced nonmetastatic adenocarcinoma of the prostate and should be considered the standard of care.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2017.02.004

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2017.02.004;
PII
S0360-3016(17)30331-0;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
98
Journal Issue
2
Journal Page Range
p. 296-303
ISSN
0360-3016
CODEN
IOBPD3

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
48098585
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
ANDROGENS; NEOPLASMS; PROSTATE; RADIOTHERAPY
Descriptors DEC
ANDROSTANES; BODY; DISEASES; GLANDS; HORMONES; MALE GENITALS; MEDICINE; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; ORGANS; RADIOLOGY; STEROID HORMONES; STEROIDS; THERAPY

Optional Information

Copyright
Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.