Huynh Mai Anh, Chen Ming-Hui, Wu Jing, Braccioforte Michelle H, Moran Brian J, D'Amico Anthony V
Harvard Radiation Oncology Program, Brigham and Women's Hospital, Boston, Massachusetts.
Department of Statistics, University of Connecticut, Storrs, Connecticut.
Int J Radiat Oncol Biol Phys. 2016 Jul 15;95(4):1158-67. doi: 10.1016/j.ijrobp.2016.03.004. Epub 2016 Mar 11.
To explore whether a subgroup of men with unfavorable-risk prostate cancer (PC) exists in whom high-dose radiation therapy (RT) alone is sufficient to avoid excess PC death due to competing risk from cardiometabolic comorbidity.
This was a cohort study of 7399 men in whom comorbidity (including congestive heart failure, diabetes mellitus, or myocardial infarction) was assessed and recorded with T1-3NxM0 PC treated with brachytherapy with or without neoadjuvant RT, October 1997 to May 2013 at a single providing institution. Cox and competing risks regression analyses were used to assess whether men with unfavorable-intermediate/high-risk versus favorable-intermediate/low-risk PC were at increased risk of PC-specific, all-cause, or other-cause mortality (PCSM, ACM, OCM), adjusting for number of comorbidities, age at and year of brachytherapy, RT use, and an RT treatment propensity score.
After a median follow-up of 7.7 years, 935 men died: 80 of PC and 855 of other causes. Among men with no comorbidity, PCSM risk (adjusted hazard ratio [AHR] 2.74 [95% confidence interval (CI) 1.49-5.06], P=.001) and ACM risk (AHR 1.30 [95% CI 1.07-1.58], P=.007) were significantly increased in men with unfavorable-intermediate/high-risk PC versus favorable-intermediate/low-risk PC, with no difference in OCM (P=.07). Although PCSM risk was increased in men with 1 comorbidity (AHR 2.87 [95% CI 1.11-7.40], P=.029), ACM risk was not (AHR 1.03 [95% CI 0.78-1.36], P=.84). Neither PCSM risk (AHR 4.39 [95% CI 0.37-51.98], P=.24) or ACM risk (AHR 1.43 [95% CI 0.83-2.45], P=.20) was increased in men with 2 comorbidities.
To minimize death from PC, high-dose RT alone may be sufficient treatment in men with 2 or more cardiometabolic comorbidities and unfavorable-intermediate- and high-risk PC.
探讨是否存在一组具有不良风险的前列腺癌(PC)男性亚组,在该亚组中单纯高剂量放射治疗(RT)足以避免因心脏代谢合并症的竞争风险导致的PC死亡过多。
这是一项对7399名男性的队列研究,于1997年10月至2013年5月在单一医疗机构对合并症(包括充血性心力衰竭、糖尿病或心肌梗死)进行评估并记录,这些男性接受了近距离放射治疗,伴或不伴新辅助RT,T1-3NxM0期PC。使用Cox和竞争风险回归分析来评估具有不良-中/高风险与良好-中/低风险PC的男性在PC特异性、全因或其他原因死亡率(PCSM、ACM、OCM)方面是否增加,同时调整合并症数量、近距离放射治疗时的年龄和年份、RT使用情况以及RT治疗倾向评分。
中位随访7.7年后,935名男性死亡:80名死于PC,855名死于其他原因。在无合并症的男性中,与良好-中/低风险PC的男性相比,不良-中/高风险PC的男性PCSM风险(调整后风险比[AHR]2.74[95%置信区间(CI)1.49-5.06],P = 0.001)和ACM风险(AHR 1.30[95%CI 1.07-1.58],P = 0.007)显著增加,OCM无差异(P = 0.07)。虽然有1种合并症的男性PCSM风险增加(AHR 2.87[95%CI 1.11-7.40],P = 0.029),但ACM风险未增加(AHR 1.03[95%CI 0.78-1.36],P = 0.84)。有2种合并症的男性PCSM风险(AHR 4.39[95%CI 0.37-51.98],P = 0.24)或ACM风险(AHR 1.43[95%CI 0.83-2.45],P = 0.20)均未增加。
为使PC死亡风险最小化,对于患有2种或更多心脏代谢合并症以及不良-中、高风险PC的男性,单纯高剂量RT可能是足够的治疗方法。