Ho Chung-Han, Cheng Kuo-Chen, Chao Chien-Ming, Lai Chih-Cheng, Chiang Shyh-Ren, Chen Chin-Ming, Liao Kuang-Ming, Wang Jhi-Joung, Lee Po-Huang, Hung Chao-Ming, Tai Chi-Ming, Chiu Chong-Chi
Department of Medical Research, Chi Mei Medical Center, Tainan 71004, Taiwan.
Department of Hospital and Health Care Administration, Chia Nan University of Pharmacy and Science, Tainan 71710, Taiwan.
J Cancer. 2020 Aug 25;11(21):6204-6212. doi: 10.7150/jca.44726. eCollection 2020.
The survival of prostate cancer (PC) patients after radiotherapy (RT) has improved over time, but it raises the debate of increased risk of secondary colorectal cancer (SCRC). This study aimed to assess whether RT for PC treatment increases the risk of SCRC in comparison with radical prostatectomy (RP). A population-based cohort of PC patients treated only with RT or only with RP between January 2007 and December 2015 was identified from the Taiwan Cancer Registry. The incidence rate of SCRC development was estimated using Cox regression model. In this study, total 8,797 PC patients treated with either RT (n = 3,219) or RP (n =5,578). Patients subjected to RT were elder (higher percentage of 70≧years, < 0.0001) and more advanced clinically (stage III: 22.90% vs. 11.87%; stage IV: 22.15% vs. 13.80%, < 0.0001), compared to those subjected to RP. More patients subjected to RT had a much higher percentage of autoimmune disease (22.34% vs. 18.75%, < 0.0001) and osteoarthritis and allied disorders (16.31% vs. 12.98%, < 0.0001). Besides, RT patients had a higher percentage of underlying Crohn's disease (0.25% vs. 0.05%, = 0.0230). Although almost all selected factors were not statistically significant, they presented the positive risk of SCRC for those under RP compared with those among RT. Besides, for PC patients in clinical stage I and II, patients with RP may have borderline significantly protective effects of SCRC compared with those under RT (stage I, HR: 0.14; 95% C.I.:0.01-1.39; = 0.0929; stage II, HR: 1.92; 95% C.I.:0.93-3.95; = 0.0775). Kaplan-Meier curves for a 3-year-period, which demonstrated no statistical difference in the risk of SCRC free between PC patients undergoing RT and RP ( = 0.9766). Whether or not pelvic RT for PC is associated with an increased risk for SCRC on a population-based level remains a matter of considerable debate. From a clinical perspective, these PC survivors should be counseled accordingly and received continued cancer surveillance with regular colonoscopy follow-up.
随着时间的推移,前列腺癌(PC)患者放疗(RT)后的生存率有所提高,但这引发了关于继发性结直肠癌(SCRC)风险增加的争论。本研究旨在评估与根治性前列腺切除术(RP)相比,PC治疗的RT是否会增加SCRC的风险。从台湾癌症登记处识别出2007年1月至2015年12月期间仅接受RT或仅接受RP治疗的PC患者的基于人群的队列。使用Cox回归模型估计SCRC发生的发病率。在本研究中,共有8797例PC患者接受了RT(n = 3219)或RP(n = 5578)治疗。与接受RP的患者相比,接受RT的患者年龄更大(70岁及以上的百分比更高,<0.0001),临床分期更晚(III期:22.90%对11.87%;IV期:22.15%对13.80%,<0.0001)。接受RT的患者中自身免疫性疾病的百分比更高(22.34%对18.75%,<0.0001),骨关节炎及相关疾病的百分比更高(16.31%对12.98%,<0.0001)。此外,RT患者潜在克罗恩病的百分比更高(0.25%对0.05%,=0.0230)。尽管几乎所有选定因素在统计学上均无显著意义,但与RT患者相比,RP患者出现SCRC的风险呈正向。此外,对于临床I期和II期的PC患者,与接受RT的患者相比,接受RP的患者对SCRC可能有临界显著保护作用(I期,HR:0.14;95%CI:0.01-1.39;=0.0929;II期,HR:1.92;95%CI:0.93-3.95;=0.0775)。3年期间的Kaplan-Meier曲线显示,接受RT和RP的PC患者无SCRC风险无统计学差异(=0.9766)。基于人群水平上,PC的盆腔RT是否与SCRC风险增加相关仍存在相当大争议。从临床角度来看,应相应地为这些PC幸存者提供咨询,并通过定期结肠镜随访进行持续癌症监测。