Department of Pharmacy, Peking University Third Hospital, Beijing, People's Republic of China.
Department of Epidemiology, Richard M. Fairbanks School of Public Health, Indiana University, 1050 Wishard Blvd, Indianapolis, IN, 46202, USA.
Diabetologia. 2017 Oct;60(10):1862-1872. doi: 10.1007/s00125-017-4370-8. Epub 2017 Jul 19.
AIMS/HYPOTHESIS: The association between sodium-glucose cotransporter 2 (SGLT2) inhibitors and the risk of cancer in individuals with type 2 diabetes remains uncertain. This study aimed to evaluate the risk of cancer associated with SGLT2 inhibitor treatment of type 2 diabetes.
We systematically searched PubMed, EMBASE, Cochrane Central Register of Controlled Trials and ClinicalTrials.gov from inception to 15 February 2017 to identify eligible randomised controlled trials (RCTs) that report cancer events in individuals with type 2 diabetes treated with SGLT2 inhibitors for at least 24 weeks. We performed pairwise and network meta-analyses as well as a cumulative meta-analysis to calculate ORs and 95% CIs.
In total, 580 incidences of cancer among 34,569 individuals were identified from 46 independent RCTs with a mean trial duration of 61 weeks. When compared with comparators (placebo or other active glucose-lowering treatments), SGLT2 inhibitors were not significantly associated with an increased risk of overall cancer (OR 1.14 [95% CI 0.96, 1.36]). For pre-specified cancer types, the risk of bladder cancer might be increased with SGLT2 inhibitors (OR 3.87 [95% CI 1.48, 10.08]), especially empagliflozin (OR 4.49 [95% CI 1.21, 16.73]). Interestingly, canagliflozin might be protective against gastrointestinal cancers (OR 0.15 [95% CI 0.04, 0.60]).
CONCLUSIONS/INTERPRETATION: Current evidence from short-term RCTs did not indicate a significantly increased risk of overall cancer among individuals with type 2 diabetes using SGLT2 inhibitors. Given the short-term trial durations and uncertainty of evidence, future long-term prospective studies and post-marketing surveillance studies are warranted.
目的/假设:钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂与 2 型糖尿病患者癌症风险之间的关联仍不确定。本研究旨在评估 SGLT2 抑制剂治疗 2 型糖尿病与癌症风险的相关性。
我们系统地检索了 PubMed、EMBASE、Cochrane 中央对照试验注册库和 ClinicalTrials.gov,从建库到 2017 年 2 月 15 日,以确定至少 24 周接受 SGLT2 抑制剂治疗的 2 型糖尿病患者中报告癌症事件的合格随机对照试验(RCT)。我们进行了成对和网络荟萃分析以及累积荟萃分析,以计算 OR 和 95%CI。
从 46 项独立的 RCT 中,共确定了 34569 例患者中的 580 例癌症病例,平均试验持续时间为 61 周。与对照组(安慰剂或其他活性降糖治疗)相比,SGLT2 抑制剂与总体癌症风险增加无关(OR 1.14 [95%CI 0.96, 1.36])。对于预先指定的癌症类型,SGLT2 抑制剂可能会增加膀胱癌的风险(OR 3.87 [95%CI 1.48, 10.08]),特别是恩格列净(OR 4.49 [95%CI 1.21, 16.73])。有趣的是,卡格列净可能对胃肠道癌症有保护作用(OR 0.15 [95%CI 0.04, 0.60])。
结论/解释:目前来自短期 RCT 的证据表明,使用 SGLT2 抑制剂的 2 型糖尿病患者总体癌症风险没有显著增加。鉴于短期试验持续时间和证据的不确定性,需要进行未来的长期前瞻性研究和上市后监测研究。