期刊
JOURNAL OF HEPATOLOGY
卷 52, 期 5, 页码 652-657出版社
ELSEVIER
DOI: 10.1016/j.jhep.2009.12.028
关键词
Hepatitis C; Hepatocellular carcinoma; Advanced fibrosis; Cirrhosis; Therapy
资金
- Schering Plough
- Gilead Sciences
- Roche
Background & Aims: Hepatocellular carcinoma (HCC) currently represents the major cause of liver-related death in patients with hepatitis C virus (HCV)-related cirrhosis. We assessed the influence of combination therapy on the risk of HCC, liver-related complications (ascites, variceal bleeding), and liver-related death (or liver transplantation). Methods: Three hundred seven chronic hepatitis C patients with bridging fibrosis (n = 127) or cirrhosis (n = 180) were evaluated by Cox regression analysis. Sustained virological response (SVR) was defined as undetectable serum HCV RNA at 24 weeks after treatment. Results: SVR developed in 33% of patients. The SVR rates were not different between patients with bridging fibrosis (37%) and those with cirrhosis (30%), p = 0.186. During a median follow-up of 3.5 years (range 1-18 years) after the last treatment, the incidence rates per 100 person-years of HCC, liver-related complications, and liver-related death, were 1.24, 0.62, and 0.61 among SVR patients, respectively, and 5.85, 4.16, and 3.76 among non-SVR patients, respectively (log-rank test, p <0.001). According to multivariate analysis, non-SVR was an independent predictor of HCC (HR 3.06; 95% CI = 1.12-8.39), liver-related complications (HR 4.73; 95% CI: 1.09-20.57), and liver-related death (HR 3.71; 95% CI = 1.05-13.05). Conclusions: SVR is achieved in one-third of patients with HCV-related cirrhosis treated with peginterferon and ribavirin. SVR has a strong independent positive influence on the incidence of HCC and on the prognosis of these patients. (C) 2010 Published by Elsevier B.V. on behalf of the European Association for the Study of the Liver.
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