| Literature DB >> 26855950 |
Arya Amini1, Brian D Kavanagh1, Chad G Rusthoven1.
Abstract
The contemporary standard of care for locally advanced high-risk prostate cancer includes a combination of dose-escalated radiotherapy (RT) plus androgen-deprivation therapy (ADT). However, 20 years ago, at the inception of the National Cancer Institute of Canada (NCIC) led study (NCIC Clinical Trials Group PR.3/Medical Research Council PR07/Intergroup T94-0110), the survival impact of prostate RT for high-risk disease was uncertain. Recently, Mason, Warde and colleagues presented the final results of this NCIC/MRC study (PMID: 25691677) randomizing 1,205 high-risk prostate cancer patients to ADT + RT vs. ADT alone. These updated results confirm substantial improvements with the addition of RT to ADT for the endpoints of overall survival (OS), disease-free survival (DFS), and biochemical recurrence. Close examination of subtleties of this trial's design highlight some of the most salient controversies in the field of prostate RT, including the risk-stratified roles of ADT, optimal ADT duration, and RT field design in the dose-escalated and intensity-modulated radiotherapy (IMRT) era.Entities:
Keywords: Androgen-deprivation therapy (ADT); dose-escalated radiotherapy; radiotherapy (RT); whole-pelvic radiotherapy (WPRT)
Year: 2016 PMID: 26855950 PMCID: PMC4716946 DOI: 10.3978/j.issn.2305-5839.2015.10.13
Source DB: PubMed Journal: Ann Transl Med ISSN: 2305-5839