Rutgers Cancer Institute of New Jersey, Rutgers, The State University of New Jersey, New Brunswick, NJ, USA.
Department of Epidemiology, School of Public Health, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
Cancer Med. 2020 Apr;9(7):2379-2389. doi: 10.1002/cam4.2862. Epub 2020 Feb 8.
Pre-clinical studies suggest that metformin and statins may delay prostate cancer (PCa) metastases; however, data in humans are limited. To the best of our knowledge, this is the first human study aimed to quantify the individual and joint effects of statin and metformin use among patients with high-risk PCa.
This population-based retrospective cohort study identified patients from the Surveillance, Epidemiology, and End Results (SEER)-Medicare linked database. Exposure to metformin and statins was ascertained from Medicare Prescription Drug Event files. The association with all-cause and PCa mortality were evaluated using Cox proportional hazard model with competing causes of death, where propensity scores were used to adjusted imbalances in covariates across groups.
Based on 12 700 patients with high-risk PCa, statin alone or in combination with metformin was significantly associated with reduced all-cause mortality (Hazard Ratio [HR]: 0.89; 95% Confidence Interval [CI]: 0.83, 0.96; and HR: 0.75; 95% CI, 0.67-0.83, respectively) and PCa mortality (HR, 0.80; 95% CI: 0.69, 0.92) and 0.64; 95% CI, d 0.51-0.81, respectively. The effects were more pronounced in post-diagnostic users: combination use of metformin/statins was associated with a 32% reduction in all-cause mortality (95% CI, 0.57-0.80), and 54% reduction in PCa mortality (95% CI, 0.30-0.69). No significant association of metformin alone was observed with either all-cause mortality or PCa mortality.
Statin use alone or in combination with metformin was associated with lower all-cause and PCa mortality among high-risk patients, particularly in post-diagnostic settings; further studies are warranted.
临床前研究表明,二甲双胍和他汀类药物可能延缓前列腺癌(PCa)转移;然而,人类数据有限。据我们所知,这是第一项旨在量化高危 PCa 患者使用他汀类药物和二甲双胍的个体和联合效应的人体研究。
这项基于人群的回顾性队列研究从监测、流行病学和最终结果(SEER)-医疗保险关联数据库中确定了患者。二甲双胍和他汀类药物的暴露情况从医疗保险处方药物事件文件中确定。使用具有竞争死亡原因的 Cox 比例风险模型评估全因死亡率和 PCa 死亡率的相关性,其中使用倾向评分调整组间协变量的不平衡。
基于 12700 名高危 PCa 患者,单独使用他汀类药物或与二甲双胍联合使用与全因死亡率降低显著相关(风险比 [HR]:0.89;95%置信区间 [CI]:0.83,0.96;和 HR:0.75;95%CI,0.67-0.83,分别)和 PCa 死亡率(HR,0.80;95%CI:0.69,0.92)和 0.64;95%CI,d 0.51-0.81,分别。在诊断后使用者中,这些效果更为明显:二甲双胍/他汀类药物联合使用与全因死亡率降低 32%相关(95%CI,0.57-0.80),PCa 死亡率降低 54%相关(95%CI,0.30-0.69)。单独使用二甲双胍与全因死亡率或 PCa 死亡率均无显著相关性。
单独使用他汀类药物或与二甲双胍联合使用与高危患者的全因死亡率和 PCa 死亡率降低相关,特别是在诊断后环境中;需要进一步研究。