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丙型肝炎病毒基因型 3 感染治疗的进展。

Developments in the treatment of HCV genotype 3 infection.

机构信息

Translational Medicine, Bristol-Myers Squibb Company , Cambridge , MA , USA.

出版信息

Expert Rev Anti Infect Ther. 2019 Oct;17(10):775-785. doi: 10.1080/14787210.2019.1676730. Epub 2019 Oct 21.

DOI:10.1080/14787210.2019.1676730
PMID:31584833
Abstract

: Unlike other hepatitis C virus (HCV) genotypes (GTs), patients infected with GT3 are associated with an increased risk of accelerated liver disease progression. Although early immuno-modulator therapies yielded moderate sustained virologic response (SVR) rates, treatment of GT3 patients has proven more challenging in the era of direct-acting antivirals (DAAs). : The review provides an overview of the evolution of therapies against GT3 since the approval of the first immunomodulatory agent nearly 30 years ago. : A greater choice of treatment options is now available for HCV GT3-infected patients. In treatment-naïve patients with or without compensated cirrhosis, SVR rates are comparably high approaching 100% irrespective of treatment option. For treatment-experienced patients, choosing the right therapy is important, especially for those with advanced liver disease. For the few patients who fail with multiple persistent highly resistant DAA substitutions, retreatment options are limited. Additional real-world treatment comparisons are required to confirm differences in SVR in these more difficult-to-treat patients. This also includes patients infected with GT3 subtypes such as GT3b where multiple DAA-resistant substitutions occur naturally. In the absence of new drugs with non-overlapping drug-resistant profiles, an interferon-based therapy may still be beneficial in select patient populations with high-level multiple DAA-resistant substitutions.

摘要

与其他丙型肝炎病毒(HCV)基因型(GT)不同,感染 GT3 的患者发生肝疾病加速进展的风险增加。虽然早期免疫调节剂治疗产生了中等程度的持续病毒学应答(SVR)率,但在直接作用抗病毒药物(DAA)时代,GT3 患者的治疗更具挑战性。

该综述概述了自近 30 年前批准首个免疫调节剂以来,针对 GT3 的治疗方法的演变。

现在,可供 HCV GT3 感染患者选择的治疗方案更多。在初治患者和伴有代偿性肝硬化的患者中,无论治疗方案如何,SVR 率均较高,接近 100%。对于治疗经验丰富的患者,选择正确的治疗方法很重要,特别是对于那些患有晚期肝病的患者。对于那些因多次持续高度耐药 DAA 替代而失败的少数患者,治疗选择有限。需要进行更多的真实世界治疗比较,以确认这些更难治疗的患者在 SVR 方面的差异。这还包括感染 GT3 亚型(如 GT3b)的患者,这些亚型天然存在多种 DAA 耐药替代。在没有具有非重叠耐药谱的新药的情况下,干扰素为基础的治疗在具有高水平多种 DAA 耐药替代的选定患者群体中仍可能有益。

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