Peg-interferon alone or combined with ribavirin in HCV cirrhosis with portal hypertension:: A randomized controlled trial

被引:73
作者
Di Marco, Vito
Almasio, Piero Luigi
Ferraro, Donatella
Calvaruso, Vincenza
Alaimo, Giuseppe
Peralta, Sergio
Di Stefano, Rosa
Craxi, Antonio
机构
[1] Cattedra Gastroenterol, Unita Operativa Complessa Gastroenterol & Epatol, I-90127 Palermo, Italy
[2] Univ Palermo, Dipartimento Igiene Microbiol, I-90133 Palermo, Italy
关键词
hepatitis C virus; cirrhosis; antiviral therapy; Peg-interferon; ribavirin; portal hypertension; clinical course; disease complications;
D O I
10.1016/j.jhep.2007.04.020
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Risks and benefits of antiviral therapy in HCV cirrhosis with portal hypertension are poorly known. Methods: We performed a randomized controlled trial in 102 HCV patients with compensated cirrhosis and portal hypertension: 51 received 1 mu g/kg/week of Pegylated-interferon alpha-2b and 51 Pegylated-interferon plus 800 mg/day of ribavirin up to 52 weeks. Results:By intention to treat analysis, five patients on monotherapy and eleven on combination therapy achieved a sustained virological response (9.8% vs. 21.6%, p = 0.06). The response was more frequent for genotypes 2 or 3 than genotype 1 (66.6% vs. 11.3%, p = 0.001). Genotype 1 who had low viral load at start of therapy, were HCV-RNA negative at 4 weeks, and were adherent to the scheduled therapy had a higher probability of sustained virological response. Patients with sustained virological response had less disease events compared to nonresponders (6.2% vs. 38.3%, p = 0.03 by log rank test) during follow-up. Conclusions: In HCV cirrhosis with portal hypertension Peg-interferon plus ribavirin is a feasible treatment. Although the rate of viral eradication is modest, tailoring by genotype and early viral response allows to keep patients on treatment who are more likely to have viral eradication. Patients with viral eradication have fewer disease complications during follow-up. (C) 2007 Published by Elsevier B.V. on behalf of the European Association for the Study of the Liver.
引用
收藏
页码:484 / 491
页数:8
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