Tangjarusritaratorn Thanida, Tangjittipokin Watip, Kunavisarut Tada
Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Siriraj Center of Research Excellence in Diabetes and Obesity, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Diabetes Metab Syndr Obes. 2021 Apr 9;14:1563-1574. doi: 10.2147/DMSO.S295753. eCollection 2021.
To evaluate metformin's benefit on the incidence and survival of hepatocellular carcinoma (HCC) in cirrhosis with type 2 diabetes mellitus (T2DM) patients.
We conducted a retrospective study from 2006 to 2019. The patients were assigned to metformin exposure if they administered metformin at least 3 months after diagnosis of cirrhosis. The outcomes were incidence and survival of HCC in T2DM with cirrhosis treated with metformin compared with those who were not treated with metformin. For the incidence of HCC, the follow-up time was 5 years after cirrhosis was diagnosed. For the survival of HCC, we censored for vital status in June 2019.
Of 1061 patients, the patients were divided into 719 patients with metformin exposure and 342 in metformin non-exposure. In metformin exposure, 125 patients (17.4%) developed HCC. In metformin non-exposure, 128 patients (37.4%) developed HCC. Metformin exposure had a significantly lower risk of developing HCC in multivariate analysis HR 0.48 (0.36-0.61); P<0.001. For the survival of HCC, 327 patients were recruited. One-hundred and sixty-two patients were in metformin exposure and 165 patients were in metformin non-exposure. Sixty patients (37%) in metformin exposure died, while 84 patients (50.9%) in metformin non-exposure died. The median survival of metformin exposure and metformin non-exposure were 6.9 years and 3.88 years, respectively; P=0.003. In univariate analysis, the metformin exposure was significantly associated with better survival than in the non-exposure group, HR 0.63 (0.45-0.88); P=0.006. No significant difference was observed in multivariate analysis between two groups, HR 1.07 (0.74-1.54); P=0.72.
Metformin exposure was associated with a lower incidence of HCC in cirrhosis with T2DM patients and seemed to extend survival. Continuing metformin in patients with cirrhosis with T2DM should be considered if there was no contraindication.
评估二甲双胍对2型糖尿病(T2DM)合并肝硬化患者肝细胞癌(HCC)发病率及生存率的影响。
我们进行了一项2006年至2019年的回顾性研究。若患者在肝硬化诊断后至少服用3个月二甲双胍,则将其纳入二甲双胍暴露组。将二甲双胍治疗的T2DM合并肝硬化患者的HCC发病率及生存率与未服用二甲双胍的患者进行比较。对于HCC发病率,随访时间为肝硬化诊断后5年。对于HCC生存率,我们以2019年6月的生命状态为截尾数据。
1061例患者中,719例为二甲双胍暴露组,342例为非暴露组。二甲双胍暴露组中,125例患者(17.4%)发生HCC。非暴露组中,128例患者(37.4%)发生HCC。多因素分析显示,二甲双胍暴露组发生HCC的风险显著较低,风险比(HR)为0.48(0.36 - 0.61);P<0.001。对于HCC生存率,共纳入327例患者。二甲双胍暴露组162例,非暴露组165例。二甲双胍暴露组60例患者(37%)死亡,非暴露组84例患者(50.9%)死亡。二甲双胍暴露组和非暴露组的中位生存期分别为6.9年和3.88年;P = 0.003。单因素分析中,二甲双胍暴露组的生存率显著高于非暴露组,HR为0.63(0.45 - 0.88);P = 0.006。多因素分析两组间无显著差异,HR为1.07(0.74 - 1.54);P = 0.72。
二甲双胍暴露与T2DM合并肝硬化患者较低的HCC发病率相关,且似乎能延长生存期。若无禁忌证,T2DM合并肝硬化患者应考虑继续使用二甲双胍。