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Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks

机译:使用病毒反应在2周内预测对基于Telaprevir的三联疗法的持续病毒学反应

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摘要

The aim of the present study was to predict sustained virological response (SVR) to telaprevir with pegylated interferon (PEG-IFN) and ribavirin using viral response within 2 weeks after therapy initiation. Thirty-six patients with genotype 1 hepatitis C virus (HCV) and high viral load were treated by telaprevir-based triple therapy. SVR was achieved in 72% (26/36) of patients. Significant differences between the SVR group and non-SVR group were noted regarding response to prior PEG-IFN plus ribavirin, interleukin (IL)28B polymorphism, amino acid substitution at core 70, cirrhosis, hyaluronic acid level, and HCV-RNA reduction within 2 weeks. Setting 4.56 logIU/mL as the cut-off value for HCV-RNA reduction at 2 weeks, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy for predicting SVR were 77%, 86%, 95%, 50%, and 79%, respectively, and for neither the IL28B minor allele nor core 70 mutant were 80%, 71%, 91%, 50%, and 78%, respectively. In conclusion, evaluation of viral reduction at 2 weeks or the combination of IL28B polymorphism and amino acid substitution at core 70 are useful for predicting SVR to telaprevir with PEG-IFN and ribavirin therapy.
机译:本研究的目的是在治疗开始后的两周内,通过病毒反应来预测聚乙二醇干扰素(PEG-IFN)和利巴韦林对特拉匹韦的持续病毒学应答(SVR)。通过基于telaprevir的三联疗法治疗了36例基因1型丙型肝炎病毒(HCV)和高病毒载量患者。 72%(26/36)的患者达到了SVR。注意到SVR组和非SVR组在对先前的PEG-IFN加利巴韦林,白介素(IL)28B多态性,70位核心氨基酸取代,肝硬化,透明质酸水平和HCV-RNA降低2之内的反应方面存在显着差异周。设定2周时HCV-RNA降低的临界值为4.56 logIU / mL,其预测SVR的敏感性,特异性,阳性预测值,阴性预测值和准确性分别为77%,86%,95%,50% IL28B小等位基因和核心70突变体分别为80%,71%,91%,50%和78%。总之,评估2周时的病毒减少或IL28B多态性与核心70位氨基酸取代的组合可用于预测PEG-IFN和利巴韦林疗法对特拉匹韦的SVR。

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