首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Successful achievement of sustained virological response to triple combination therapy containing simeprevir in two patients with chronic hepatitis C who had failed asunaprevir:Daclatasvir combination therapy
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Successful achievement of sustained virological response to triple combination therapy containing simeprevir in two patients with chronic hepatitis C who had failed asunaprevir:Daclatasvir combination therapy

机译:成功地在两名接受Asunaprevir:Daclatasvir联合治疗失败的慢性丙型肝炎患者中成功完成了包含simeprevir的三联联合治疗的持续病毒学应答

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摘要

Patients 1 and 2 were treatment-naive women who had genotype 1b chronic hepatitis C. Both had IL-28B genotype TT, and amino acid substitutions of core 70 and 91 were both wild type. Search for the presence of resistance-associated variants (RAV) in non-structural (NS)3 and NS5A regions confirmed wild-type D168 and L31, along with Y93H, in both patients. These patients participated in a Japanese phase III clinical study of asunaprevir and daclatasvir at the age of 52 and 67years, respectively, and were treated with the combination regimen for 24weeks. However, both experienced post-treatment relapse, and then treated with triple combination therapy with simeprevir, pegylated interferon (IFN) and ribavirin at the age of 53 and 68years, respectively, and achieved sustained virological response. A search for RAV prior to simeprevir treatment identified multiple resistance including D168E, Y93H and L31V in both patients. It has been demonstrated that, in many cases, a treatment failure with a combination of asunaprevir and daclatasvir results in acquisition of RAV in NS3 and NS5A regions and that drug-resistant mutants, particularly those in the NS5A region, survive for a long time. In these cases, direct-acting antivirals targeted towards the NS5A region may have a limited efficacy. The present case report is based on an idea that a regimen containing IFN with simeprevir could be a therapeutic option particularly for those who are likely to be highly sensitive and tolerable to IFN.
机译:患者1和2是未经治疗的女性,其基因型为1b慢性丙型肝炎。均具有IL-28B基因型TT,并且核心70和91的氨​​基酸替代均为野生型。寻找在非结构性(NS)3和NS5A区域中存在抗药性相关变异(RAV)的方法,在这两名患者中均确认了野生型D168和L31以及Y93H。这些患者分别在52岁和67岁时参加了Asunaprevir和daclatasvir的日本III期临床研究,并接受了联合治疗24周。然而,两者均经历了治疗后的复发,然后分别在53岁和68岁时分别接受simeprevir,聚乙二醇化干扰素(IFN)和利巴韦林的三联疗法治疗,并获得了持续的病毒学应答。在西美普韦治疗之前对RAV的搜索确定了两名患者的多重耐药性,包括D168E,Y93H和L31V。已经证明,在许多情况下,使用asunaprevir和daclatasvir的组合治疗失败会导致在NS3和NS5A区获得RAV,并且耐药突变株,尤其是NS5A区的耐药突变株可以长期存活。在这些情况下,靶向NS5A区的直接作用抗病毒药可能疗效有限。本病例报告基于这样的想法,即含有IFN与simeprevir的治疗方案可能是一种治疗选择,特别是对于那些可能对IFN高度敏感和耐受的患者。

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