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如何优化丙型肝炎病毒基因型 1 患者的现有治疗方案。基于干扰素的治疗方案与第二代直接作用抗病毒药物应答的预测因子。

How to optimize current therapy in hepatitis C virus genotype 1 patients. Predictors of response to interferon-based therapy with second wave direct acting antivirals.

机构信息

Service d'Hépatologie, Hôpital Saint-Antoine, APHP, UPMC Paris 6, Paris, France.

出版信息

Liver Int. 2015 Jan;35 Suppl 1:18-20. doi: 10.1111/liv.12722.

Abstract

Second wave direct acting antivirals such as sofosbuvir, simeprevir and daclatasvir can be combined with pegylated interferon alpha and ribavirin (PEG-IFN/RBV) as triple therapy in patients with hepatitis C virus (HCV) infection. In patients with HCV genotype 1 (HCV-1), a PEG-IFN/RBV-based regimen with sofosbuvir is highly effective but the presence of cirrhosis and the non-CC IFNL3 genotype have been associated with a poorer response. A PEG-IFN/RBV-based regimen with simeprevir or daclatasvir is based on response-guided therapy and its efficacy depends on predictors of response to IFN. HCV-1 subtype is also a major predictor of response. In HCV-1a infected patients, the K80Q mutation in NS3 or the presence of NS5A variants at baseline are associated with poor response with simeprevir- or daclatasvir-containing regimens respectively. Thus, these regimens should be only used in HCV-1b patients with good predictors of response to IFN.

摘要

第二代直接作用抗病毒药物如索非布韦、西美瑞韦和达卡他韦可与聚乙二醇干扰素α和利巴韦林(PEG-IFN/RBV)联合用于丙型肝炎病毒(HCV)感染患者的三联治疗。在 HCV-1 型(HCV-1)患者中,基于 PEG-IFN/RBV 的索非布韦方案具有很高的疗效,但肝硬化的存在和非 CC IFNL3 基因型与较差的反应相关。基于西美瑞韦或达卡他韦的 PEG-IFN/RBV 方案基于应答指导治疗,其疗效取决于对 IFN 反应的预测因素。HCV-1 亚型也是反应的主要预测因素。在 HCV-1a 感染患者中,NS3 中的 K80Q 突变或基线时 NS5A 变异的存在分别与西美瑞韦或达卡他韦方案的不良反应相关。因此,这些方案仅应在对 IFN 反应有良好预测因素的 HCV-1b 患者中使用。

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