Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital, Yun-Lin Branch, Yunlin, Taiwan.
Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital, No. 7 Chung-Shan South Road, Taipei 10002, Taiwan.
Int J Endocrinol. 2014;2014:719578. doi: 10.1155/2014/719578. Epub 2014 Aug 31.
Risk of increasing breast and bladder cancer remains a safety issue of SGLT2 (sodium glucose cotransporter type 2) inhibitors, a novel class of antidiabetic agent. We reviewed related papers published before January 29, 2014, through Pubmed search. Dapagliflozin and canagliflozin are the first two approved SGLT2 inhibitors for diabetes therapy. Although preclinical animal toxicology did not suggest a cancer risk of dapagliflozin and overall tumor did not increase, excess numbers of female breast cancer and male bladder cancer were noted in preclinical trials (without statistical significance). This concern of cancer risk hindered its approval by the US FDA in January, 2012. New clinical data suggested that the imbalance of bladder and breast cancer might be due to early diagnosis rather than a real increase of cancer incidence. No increased risk of overall bladder or breast cancer was noted for canagliflozin. Therefore, the imbalance observed with dapagliflozin treatment should not be considered as a class effect of SGLT2 inhibitors and the relationship with cancer for each specific SGLT2 inhibitor should be examined individually. Relationship between SGLT2 inhibition and cancer formation is still inconclusive and studies with larger sample size, longer exposure duration, and different ethnicities are warranted.
SGLT2(钠-葡萄糖共转运蛋白 2)抑制剂作为新型降糖药物,增加乳腺癌和膀胱癌风险仍是安全性问题。我们通过 Pubmed 检索,对截至 2014 年 1 月 29 日以前发表的相关文献进行了复习。达格列净和卡格列净是获批用于糖尿病治疗的前两种 SGLT2 抑制剂。虽然临床前动物毒理学研究未提示达格列净有致癌风险,整体肿瘤也未见增加,但临床前试验中注意到女性乳腺癌和男性膀胱癌的例数增加(无统计学意义)。这一致癌风险的担忧导致美国 FDA 于 2012 年 1 月不予批准。新的临床数据提示,膀胱癌和乳腺癌的失衡可能是由于早期诊断,而非癌症发病率的真实增加。卡格列净并未增加膀胱癌或乳腺癌的总体风险。因此,达格列净治疗中观察到的这种失衡不应被认为是 SGLT2 抑制剂的类效应,而应单独检查每种特定 SGLT2 抑制剂的致癌风险。SGLT2 抑制与癌症形成之间的关系仍不确定,需要开展具有更大样本量、更长暴露时间和不同种族的研究。