Departments of Surgery, Hepatology, and Nutrition, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.
Hepatology. 2012 Jun;55(6):1809-19. doi: 10.1002/hep.25536. Epub 2012 Apr 23.
Concomitant increasing incidences of hepatocellular carcinoma (HCC) and nonalcoholic steatohepatitis (NASH) suggest that a substantial proportion of HCC arises as a result of hepatocellular injury from NASH. The aim of this study was to determine differences in severity of liver dysfunction at HCC diagnosis and long-term survival outcomes between patients undergoing curative therapy for HCC in the background of NASH compared to hepatitis C virus (HCV) and/or alcoholic liver disease (ALD). Patient demographics and comorbidities, clinicopathologic data, and long-term outcomes among patients who underwent liver transplantation, hepatic resection, or radiofrequency ablation for HCC were reviewed. From 2000 to 2010, 303 patients underwent curative treatment of HCC; 52 (17.2%) and 162 (53.5%) patients had NASH and HCV and/or alcoholic liver disease. At HCC diagnosis, NASH patients were older (median age 65 versus 58 years), were more often female (48.1% versus 16.7%), more often had the metabolic syndrome (45.1% versus 14.8%), and had lower model for end-stage liver disease scores (median 9 versus 10) (all P < 0.05). NASH patients were less likely to have hepatic bridging fibrosis or cirrhosis (73.1% versus 93.8%; P < 0.001). After a median follow-up of 50 months after curative treatment, the most frequent cause of death was liver failure. Though there were no differences in recurrence-free survival after curative therapy (median, 60 versus 56 months; P = 0.303), NASH patients had longer overall survival (OS) (median not reached versus 52 months; P = 0.009) independent of other clinicopathologic factors and type of curative treatment.
Patients with HCC in the setting of NASH have less severe liver dysfunction at HCC diagnosis and better OS after curative treatment compared to counterparts with HCV and/or alcoholic liver disease.
肝细胞癌(HCC)和非酒精性脂肪性肝炎(NASH)的发病率同时升高,这表明相当一部分 HCC 是由 NASH 导致的肝细胞损伤引起的。本研究旨在确定与丙型肝炎病毒(HCV)和/或酒精性肝病(ALD)相比,NASH 背景下接受 HCC 根治性治疗的患者在 HCC 诊断时肝功能障碍的严重程度差异以及长期生存结局。我们回顾了接受肝移植、肝切除术或射频消融术治疗 HCC 的患者的人口统计学和合并症、临床病理数据以及长期结果。
2000 年至 2010 年,303 例患者接受 HCC 根治性治疗;52(17.2%)和 162(53.5%)例患者患有 NASH 和 HCV 和/或酒精性肝病。在 HCC 诊断时,NASH 患者年龄较大(中位年龄 65 岁 vs. 58 岁),女性更多(48.1% vs. 16.7%),更常患有代谢综合征(45.1% vs. 14.8%),并且模型用于评估终末期肝病的评分较低(中位数 9 分 vs. 10 分)(均 P <0.05)。NASH 患者发生肝桥纤维化或肝硬化的可能性较小(73.1% vs. 93.8%;P <0.001)。在根治性治疗后中位随访 50 个月后,最常见的死亡原因为肝功能衰竭。尽管根治性治疗后无复发生存率无差异(中位时间,60 个月 vs. 56 个月;P = 0.303),但 NASH 患者的总生存(OS)时间更长(中位数未达到 vs. 52 个月;P = 0.009),独立于其他临床病理因素和根治性治疗类型。
与 HCV 和/或酒精性肝病相比,NASH 背景下的 HCC 患者在 HCC 诊断时肝功能障碍较轻,根治性治疗后 OS 更好。