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达卡他韦治疗丙型肝炎的疗效与安全性概述

Efficacy and Safety of Daclatasvir in Hepatitis C: An Overview.

作者信息

Gamal Nesrine, Gitto Stefano, Andreone Pietro

机构信息

Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.

出版信息

J Clin Transl Hepatol. 2016 Dec 28;4(4):336-344. doi: 10.14218/JCTH.2016.00038. Epub 2016 Nov 3.

DOI:10.14218/JCTH.2016.00038
PMID:28097103
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5225154/
Abstract

Hepatitis C virus (HCV) infection is a growing public health concern, with 184 million people infected worldwide. During the past decade, interferon has been the backbone of HCV treatment, even though it remains far from ideal. The latest development of the new direct antivirals has drastically changed the treatment approach for chronic hepatitis C (CHC). Inhibitors of the HCV NS5A region have garnered remarkable interest among treating physicians, due to their high potency and favourable safety profile. In particular, treatment with daclatasvir (DCV) has yielded high rates of vriologic response in patients infected with genotype (Gt) 1 and Gt 3, when used in combination with other antivirals of a different class, such as sofosbuvir. Although few data are available for DCV treatment of the other Gts, the results in patients with Gt 2 and Gt 4 infection appear promising, as do those for unique patient populations. NS5A-resistant viral variants can pre-exist or emerge after treatment failure for the HCV NS5A inhibitors. Nonetheless, DCV-resistant viral variants continue to be sensitive to interferon and other classes of antivirals such as NS3/4A and NS5B inhibitors. Herein, we aimed to provide an overview of the current knowledge about DCV in the treatment of CHC.

摘要

丙型肝炎病毒(HCV)感染是一个日益严重的公共卫生问题,全球有1.84亿人感染。在过去十年中,干扰素一直是HCV治疗的主要药物,尽管它仍远非理想。新型直接抗病毒药物的最新发展极大地改变了慢性丙型肝炎(CHC)的治疗方法。HCV NS5A区域的抑制剂因其高效力和良好的安全性,在治疗医生中引起了极大的兴趣。特别是,当与其他不同类别的抗病毒药物(如索磷布韦)联合使用时,使用达卡他韦(DCV)治疗基因型(Gt)1和Gt 3感染的患者产生了高病毒学应答率。虽然关于DCV治疗其他Gt的数据很少,但Gt 2和Gt 4感染患者的结果以及独特患者群体的结果似乎很有希望。NS5A耐药病毒变体可以在HCV NS5A抑制剂治疗失败之前就存在或出现。尽管如此,DCV耐药病毒变体仍然对干扰素和其他类别的抗病毒药物(如NS3/4A和NS5B抑制剂)敏感。在此,我们旨在概述目前关于DCV治疗CHC的知识。

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本文引用的文献

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Daclatasvir plus sofosbuvir, with or without ribavirin, achieved high sustained virological response rates in patients with HCV infection and advanced liver disease in a real-world cohort.在一个真实世界队列中,对于丙型肝炎病毒(HCV)感染且患有晚期肝病的患者,达卡他韦联合索磷布韦,无论是否联用利巴韦林,均实现了较高的持续病毒学应答率。
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Daclatasvir combined with sofosbuvir or simeprevir in liver transplant recipients with severe recurrent hepatitis C infection.在患有严重复发性丙型肝炎感染的肝移植受者中,将达卡他韦与索磷布韦或simeprevir联合使用。
Liver Transpl. 2016 Apr;22(4):446-58. doi: 10.1002/lt.24416.
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Safety and efficacy of dual direct-acting antiviral therapy (daclatasvir and asunaprevir) for chronic hepatitis C virus genotype 1 infection in patients on hemodialysis.直接抗病毒药物(达拉他韦和阿舒瑞韦)联合治疗方案治疗慢性丙型肝炎病毒 1 型感染合并血液透析患者的安全性和疗效。
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Efficacy and safety of daclatasvir and asunaprevir combination therapy in chronic hemodialysis patients with chronic hepatitis C.达卡他韦和asunaprevir 联合治疗方案治疗慢性丙型肝炎合并慢性血液透析患者的疗效和安全性。
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Interferon-free treatment with sofosbuvir/daclatasvir achieves sustained virologic response in 100% of HIV/hepatitis C virus-coinfected patients with advanced liver disease.索磷布韦/达卡他韦无干扰素治疗使100%的晚期肝病HIV/丙型肝炎病毒合并感染患者获得持续病毒学应答。
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