Published November 15, 2011 | Version v1
Journal article

Continued Benefit to Androgen Deprivation Therapy for Prostate Cancer Patients Treated With Dose-Escalated Radiation Therapy Across Multiple Definitions of High-Risk Disease

  • 1. Department of Radiation Oncology, University of Michigan, Ann Arbor, MI (United States)
  • 2. Department of Radiation Oncology, Cedars Sinai Medical Center, Los Angeles, CA (United States)
  • 3. Department of Radiology, Ann Arbor VA Medical Center, Ann Arbor, MI (United States)

Description

Purpose: To analyze prognostic factors in patients with high-risk prostate cancer treated with dose-escalated external-beam radiation therapy (EBRT) and androgen deprivation (ADT). Methods and Materials: Between 1998 and 2008 at University of Michigan Medical Center, 718 men were consecutively treated with EBRT to at least 75 Gy. Seven definitions of high-risk prostate cancer, applying to 11–33% of patients, were evaluated. Biochemical failure (BF), salvage ADT use, metastatic progression, and prostate cancer–specific mortality (PCSM) were estimated by the Kaplan-Meier method and Cox proportional hazards regression. Results: Each high-risk definition was associated with increased BF (hazard ratio [HR] 2.8–3.9, p < 0.0001), salvage ADT use (HR 3.9–6.3, p < 0.0001), metastasis (HR 3.7–6.6, p < 0.0001), and PCSM (HR 3.7–16.2, p < 0.0001). Furthermore, an increasing number of high-risk features predicted worse outcome. Adjuvant ADT yielded significant reductions in both metastases (HR 0.19–0.38, p < 0.001) and PCSM (HR 0.38–0.50, p < 0.05) for all high-risk definitions (with the exception of clinical Stage T3–4 disease) but improved BF only for those with elevated Gleason scores (p < 0.03, HR 0.25–0.48). When treated with ADT and dose-escalated EBRT, patients with Gleason scores 8 to 10, without other high-risk features, had 8-year freedom from BF of 74%, freedom from distant metastases of 93%, and cause-specific survival of 92%, with salvage ADT used in 16% of patients. Conclusion: Adjuvant ADT results in a significant improvement in clinical progression and PCSM across multiple definitions of high-risk disease even with dose-escalated EBRT. There is a subset of patients, characterized by multiple high-risk features or the presence of Gleason Pattern 5, who remain at significant risk for metastasis and PCSM despite current treatment.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.ijrobp.2011.04.037

Additional details

Identifiers

DOI
10.1016/j.ijrobp.2011.04.037;
PII
S0360-3016(11)00558-X;

Publishing Information

Journal Title
International Journal of Radiation Oncology, Biology and Physics
Journal Volume
81
Journal Issue
4
Journal Page Range
p. e335-e344
ISSN
0360-3016
CODEN
IOBPD3

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
44014353
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
ANDROGENS; HAZARDS; MEN; METASTASES; MORTALITY; NEOPLASMS; PATIENTS; PROSTATE; RADIATION DOSES; RADIOTHERAPY
Descriptors DEC
ANDROSTANES; ANIMALS; BODY; DISEASES; DOSES; GLANDS; HORMONES; MALE GENITALS; MALES; MAMMALS; MAN; MEDICINE; NUCLEAR MEDICINE; ORGANIC COMPOUNDS; ORGANS; PRIMATES; RADIOLOGY; STEROID HORMONES; STEROIDS; THERAPY; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.