Department of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Ann Transl Med. 2016 Jan;4(1):14. doi: 10.3978/j.issn.2305-5839.2015.10.13.
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.
当代局部晚期高危前列腺癌的标准治疗包括剂量递增放疗 (RT) 加雄激素剥夺治疗 (ADT)。然而,20 年前,在加拿大国家癌症研究所 (NCIC) 牵头的研究 (NCIC 临床试验组 PR.3/医学研究委员会 PR07/联合 T94-0110) 开始时,前列腺 RT 治疗高危疾病的生存影响尚不确定。最近,Mason、Warde 和同事公布了这项 NCIC/MRC 研究的最终结果 (PMID: 25691677),该研究将 1205 例高危前列腺癌患者随机分为 ADT+RT 组与 ADT 组。这些更新的结果证实,ADT 联合 RT 治疗可显著改善总生存 (OS)、无病生存 (DFS) 和生化复发等终点。仔细研究该试验设计的细微差别,突出了前列腺 RT 领域的一些最突出的争议,包括 ADT 的风险分层作用、最佳 ADT 持续时间以及在调强放疗 (IMRT) 时代的 RT 野设计。