Wang Yiran, Li Zonglin, Lin Chu, Zhou Jinyu, Cai Xiaoling, Lv Fang, Yang Wenjia, Ji Linong
Department of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.
Expert Rev Clin Pharmacol. 2025 Mar;18(3):165-173. doi: 10.1080/17512433.2024.2439970. Epub 2025 Feb 4.
To evaluate the association between sodium-glucose cotransporter-2 inhibitors (SGLT-2i) and the risk of neoplasm in patients with Type 2 diabetes (T2D).
Literature retrieval was conducted using databases from inception to June 2024. Randomized controlled trials (RCTs) comparing SGLT-2i with placebo or other treatments in patients with T2D, and with reports of neoplasm events were included. Results were computed as the risk ratio (RR) with 95% confidence intervals (CI).
A total of 53 RCTs with 126,232 participants were included. No significant differences were found for the risk of overall neoplasm (RR = 1.08, 95% CI: 0.99 to 1.19, I = 23%) in patients with SGLT-2i treatment compared with non-users. However, decreased risk of pulmonary neoplasm (RR = 0.83, 95% CI: 0.69 to 0.99, I = 0.0%) was observed in SGLT-2i users compared to non-users, while increased risk of prostate neoplasm in SGLT-2i users was found (RR = 1.21, 95% CI: 1.00 to 1.47, I = 0.0%).
Compared with non-users, the use of SGLT-2i was not associated with the risk of overall neoplasm. However, pulmonary neoplasms were less frequent in SGLT-2i users, while an increased risk of prostate neoplasm was observed in SGLT-2i users compared to non-users.
www.crd.york.ac.uk/prospero identifier is CRD42021273681.
评估钠-葡萄糖协同转运蛋白2抑制剂(SGLT-2i)与2型糖尿病(T2D)患者发生肿瘤的风险之间的关联。
使用自建库至2024年6月的数据库进行文献检索。纳入比较SGLT-2i与安慰剂或其他治疗方法治疗T2D患者的随机对照试验(RCT),以及有肿瘤事件报告的研究。结果计算为风险比(RR)及95%置信区间(CI)。
共纳入53项RCT,涉及126,232名参与者。与未使用SGLT-2i的患者相比,使用SGLT-2i治疗的患者总体肿瘤风险无显著差异(RR = 1.08,95% CI:0.99至1.19,I² = 23%)。然而,与未使用者相比,SGLT-2i使用者的肺部肿瘤风险降低(RR = 0.83,95% CI:0.69至0.99,I² = 0.0%),而SGLT-2i使用者的前列腺肿瘤风险增加(RR = 1.21,95% CI:1.00至1.47,I² = 0.0%)。
与未使用者相比,使用SGLT-2i与总体肿瘤风险无关。然而,SGLT-2i使用者的肺部肿瘤发生率较低,而与未使用者相比,SGLT-2i使用者的前列腺肿瘤风险增加。