Li Yan-Rong, Liu Chi-Hung, Sun Wei-Chiao, Fan Pei-Yi, Liu Feng-Hsuan, Chen Tien-Hsing, Wu Victor Chien-Chia, Lin Chihung, Hsiao Ching-Chung
Division of Endocrinology and Metabolism, Department of Internal Medicine, Linkou Chang Gung Memorial Hospital, Taoyuan 333, Taiwan.
College of Medicine, Chang Gung University, Taoyuan 333, Taiwan.
J Pers Med. 2021 Aug 24;11(9):828. doi: 10.3390/jpm11090828.
Either sodium-glucose cotransporter-2 (SGLT-2) inhibitors or pioglitazone (Pio) has doubtful issues of bladder cancer, especially for the combination therapy with these two drugs. Our study aimed to investigate the risk of bladder cancer under combination therapy of SGLT-2 inhibitors and Pio. We included 97,024 patients with type 2 diabetes mellitus (T2DM) in the Chang Gung Research Database in Taiwan from 1 January 2016 to 31 December 2019. The primary outcome was newly diagnosed bladder cancer after combination therapy with SGLT-2 inhibitors and Pio. Group 1 received both study drugs, group 2 received SGLT-2 inhibitors, group 3 received Pio, and group 4 received non-study drugs (the reference group). The secondary outcome in each group was all-cause mortality. Results: In group 1, no newly diagnosed bladder cancer was detected after a mean 2.8-year follow-up and all-cause mortality decreased significantly (adjusted hazard ratio (AHR), 0.70; 95% confidence interval (CI), 0.54-0.92) in comparison to the reference group (group 4). In group 2 and group 3, no trend of increased bladder cancer was observed (group 2: AHR 0.49, 95% CI 0.05-4.94; group 3: AHR 0.48, 95% CI 0.15-1.58) and it still reduced all-cause mortality (group 2: AHR 0.83, 95% CI 0.70-0.99; group 3: AHR 0.90, 95% CI 0.83-0.99). In T2DM patients without previous or active bladder cancer, the combination therapy of SGLT-2 inhibitors and Pio was not associated with newly diagnosed bladder cancer and had lower all-cause mortality.
钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂或吡格列酮(Pio)都存在膀胱癌方面的可疑问题,尤其是这两种药物联合使用时。我们的研究旨在调查SGLT-2抑制剂与Pio联合治疗下膀胱癌的风险。我们纳入了台湾长庚研究数据库中2016年1月1日至2019年12月31日期间的97024例2型糖尿病(T2DM)患者。主要结局是SGLT-2抑制剂与Pio联合治疗后新诊断的膀胱癌。第1组接受两种研究药物,第2组接受SGLT-2抑制剂,第3组接受Pio,第4组接受非研究药物(参照组)。每组的次要结局是全因死亡率。结果:在第1组中,平均2.8年的随访后未检测到新诊断的膀胱癌,与参照组(第4组)相比,全因死亡率显著降低(调整后风险比(AHR),0.70;95%置信区间(CI),0.54 - 0.92)。在第2组和第3组中,未观察到膀胱癌增加的趋势(第2组:AHR 0.49,95% CI 0.05 - 4.94;第3组:AHR 0.48,95% CI 0.15 - 1.58),且全因死亡率仍有所降低(第2组:AHR 0.83,95% CI 0.70 - 0.99;第3组:AHR 0.90,95% CI 0.83 - 0.99)。在既往无膀胱癌或当前无活动性膀胱癌的T2DM患者中,SGLT-2抑制剂与Pio联合治疗与新诊断的膀胱癌无关,且全因死亡率较低。