Farnik Harald, Mihm Ulrike, Zeuzem Stefan
Department of Medicine I, J.W. Goethe University Hospital, Frankfurt, Germany.
Liver Int. 2009 Jan;29 Suppl 1:23-30. doi: 10.1111/j.1478-3231.2008.01969.x.
Most infections with hepatitis C virus (HCV) fail to resolve spontaneously and progress to chronic hepatitis C. Genotype 1 HCV accounts for most hepatitis C infections in North America, Western Europe, and Japan. Patients infected with HCV genotype 1 are the most resistant to treatment, which results in poor treatment outcomes. Although sustained virologic response (SVR) rates have significantly improved with introduction of combination therapy with pegylated interferon alfa and ribavirin, the rates are still lower than those in genotype 2 or 3 infections. This review discusses how treatment outcomes in patients with HCV genotype 1 infection can be optimized by using the drugs currently licensed for treatment of hepatitis C: pegylated interferon alfa-2a/b and ribavirin. Dose modifications and variations of treatment duration are the two strategies that have been investigated best, so far. Treatment--naïve patients and non-responders and relapsers to prior antiviral therapy are discussed separately.
大多数丙型肝炎病毒(HCV)感染无法自发清除,会进展为慢性丙型肝炎。1型HCV在北美、西欧和日本的丙型肝炎感染中占大多数。感染1型HCV的患者对治疗最具抗性,导致治疗效果不佳。尽管聚乙二醇化干扰素α与利巴韦林联合治疗的持续病毒学应答(SVR)率已显著提高,但仍低于2型或3型感染的应答率。本综述讨论了如何通过使用目前已获许可用于治疗丙型肝炎的药物:聚乙二醇化干扰素α-2a/b和利巴韦林,来优化1型HCV感染患者的治疗效果。剂量调整和治疗疗程的变化是迄今为止研究得最为充分的两种策略。初治患者以及既往抗病毒治疗无应答者和复发者将分别进行讨论。