Bhat Mamatha, Chaiteerakij Roongruedee, Harmsen William S, Schleck Cathy D, Yang Ju Dong, Giama Nasra H, Therneau Terry M, Gores Gregory J, Roberts Lewis R
Mamatha Bhat, Roongruedee Chaiteerakij, Ju Dong Yang, Nasra H Giama, Gregory J Gores, Lewis R Roberts, Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, MN 55902, United States.
World J Gastroenterol. 2014 Nov 14;20(42):15750-5. doi: 10.3748/wjg.v20.i42.15750.
To assess whether metformin, which has a chemopreventive effect in chronic liver disease, has any chemotherapeutic effect in hepatocellular carcinoma.
This was a retrospective study of 701 patients with newly diagnosed hepatocellular carcinoma (HCC) seen between January 2005 and June 2011 at Mayo Clinic, Rochester, Minnesota. This patient cohort was a part of the global HCC BRIDGE study, which is a large longitudinal study of HCC determining the real-world experience of HCC characteristics, management and patient outcomes. We defined significant metformin exposure as continuation of this agent at least 90 d beyond diagnosis of HCC, and compared survival of diabetic patients on metformin to diabetic patients not on metformin and non-diabetics.
Our cohort was 72.9% male, with a mean ± SD age of 62.6 ± 12.3 years. The most common etiologies of liver disease were hepatitis C (34%), alcoholic liver disease (29%), fatty liver disease (15%) and hepatitis B (9%). By univariate analysis, using diabetics not on metformin as the reference group, diabetic patients with HCC on metformin had no survival advantage, with a HR (95%CI) of 1.0 (0.8-1.3). Non-diabetic HCC patients also did not appear to have a survival advantage as compared to diabetic HCC patients not on metformin, as demonstrated by a HR (95%CI) of 1.1 (0.7-1.7). Diabetics on metformin beyond 90 d after HCC diagnosis had a longer median survival at 34.2 mo, as compared to 25.5 mo among diabetic patients who were not on metformin or had discontinued metformin within 90 d after HCC diagnosis. This finding was likely due to potential survival bias among those who lived long enough to receive metformin.
Although the literature suggests a chemotherapeutic effect in other malignancies, our study demonstrates no survival benefit to the use of metformin in diabetic patients with HCC.
评估在慢性肝病中具有化学预防作用的二甲双胍对肝细胞癌是否具有任何化疗效果。
这是一项对2005年1月至2011年6月间在明尼苏达州罗切斯特市梅奥诊所就诊的701例新诊断肝细胞癌(HCC)患者的回顾性研究。该患者队列是全球HCC BRIDGE研究的一部分,这是一项关于HCC的大型纵向研究,旨在确定HCC特征、管理及患者预后的实际情况。我们将显著二甲双胍暴露定义为在HCC诊断后至少持续使用该药物90天,并比较使用二甲双胍的糖尿病患者与未使用二甲双胍的糖尿病患者及非糖尿病患者的生存率。
我们的队列中男性占72.9%,平均年龄±标准差为62.6±12.3岁。肝病的最常见病因是丙型肝炎(34%)、酒精性肝病(29%)、脂肪性肝病(15%)和乙型肝炎(9%)。单因素分析中,以未使用二甲双胍的糖尿病患者作为参照组,使用二甲双胍的HCC糖尿病患者没有生存优势,风险比(95%置信区间)为1.0(0.8 - 1.3)。与未使用二甲双胍的HCC糖尿病患者相比,非糖尿病HCC患者似乎也没有生存优势,风险比(95%置信区间)为1.1(0.7 - 1.7)。HCC诊断后使用二甲双胍超过90天的糖尿病患者中位生存期更长,为34.2个月,而未使用二甲双胍或在HCC诊断后90天内停用二甲双胍的糖尿病患者中位生存期为25.5个月。这一发现可能是由于那些存活时间足够长以接受二甲双胍治疗的患者存在潜在的生存偏倚。
尽管文献表明二甲双胍在其他恶性肿瘤中具有化疗效果,但我们的研究表明,在HCC糖尿病患者中使用二甲双胍并无生存益处。