Centre for Public Health, Queen's University Belfast, Belfast, UK.
School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
Int J Cancer. 2024 Aug 15;155(4):666-674. doi: 10.1002/ijc.34937. Epub 2024 Mar 30.
Pre-clinical evidence suggests that 5-alpha reductase inhibitors (5ARi's), prescribed in the treatment of benign prostatic hyperplasia, reduce colorectal and gastro-oesophageal cancer incidence via action on the male hormonal pathway. However, few studies to date have investigated this association at the population level. Our study aimed to investigate the risk of colorectal and gastro-oesophageal cancers with the use of 5ARi's. We conducted a retrospective cohort study of new users of 5ARi's and alpha-blockers among patients with benign prostatic hyperplasia in the UK Clinical Practice Research Datalink. Patients were followed until a first ever diagnosis of colorectal or gastro-oesophageal cancer, death from any cause or end of registration with the general practice or 31st of December 2017. Cox proportional hazards models with inverse probability of treatment weights were used to calculate weighted hazard ratios (HR) and 95% confidence intervals (CIs) of incident colorectal cancer or gastro-oesophageal cancer associated with the use of 5ARi's compared to alpha-blockers. During a mean follow-up of 6.6 years, we found no association between the use of 5ARi's and colorectal (HR: 1.13, 95% CI 0.91-1.41) or gastro-oesophageal (HR 1.14, 95% CI 0.76-1.63) cancer risk compared to alpha-blockers. Sensitivity analysis showed largely consistent results when varying lag periods, using multiple imputations, and accounting for competing risk of death. Our study found no association between the use of 5ARi's and risk of colorectal or gastro-oesophageal cancer in men with benign prostatic hyperplasia.
临床前证据表明,5α-还原酶抑制剂(5ARI)用于治疗良性前列腺增生症,通过作用于男性激素途径降低结直肠癌和胃食管交界处癌的发病率。然而,迄今为止,很少有研究在人群水平上对此相关性进行研究。我们的研究旨在调查使用 5ARI 治疗良性前列腺增生症患者的结直肠癌和胃食管交界处癌的风险。我们在英国临床实践研究数据链中进行了一项新的使用 5ARI 和α-受体阻滞剂的良性前列腺增生症患者的回顾性队列研究。患者随访至首次诊断为结直肠癌或胃食管交界处癌、任何原因死亡或普通科医生登记结束或 2017 年 12 月 31 日。使用逆概率治疗权重的 Cox 比例风险模型计算了与使用 5ARI 相比,使用α-受体阻滞剂与结直肠癌或胃食管交界处癌相关的加权风险比(HR)和 95%置信区间(CI)。在平均 6.6 年的随访中,我们发现使用 5ARI 与结直肠癌(HR:1.13,95%CI 0.91-1.41)或胃食管交界处癌(HR 1.14,95%CI 0.76-1.63)风险之间没有关联与α-受体阻滞剂相比。敏感性分析表明,在改变滞后期、使用多次插补和考虑死亡竞争风险时,结果基本一致。我们的研究发现,在患有良性前列腺增生症的男性中,使用 5ARI 与结直肠癌或胃食管交界处癌的风险之间没有关联。