首页> 外文期刊>Canadian journal of gastroenterology & hepatology. >Real World Experience of Chronic Hepatitis C Retreatment with Genotype Specific Regimens in Nonresponders to Previous Interferon-Free Therapy
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Real World Experience of Chronic Hepatitis C Retreatment with Genotype Specific Regimens in Nonresponders to Previous Interferon-Free Therapy

机译:慢性丙型肝炎的真实世界经验与非反应者基因型特异性方案对先前干扰素治疗

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Background and Aim. The development of interferon- (IFN-) free regimens substantially improved efficacy of treatment for HCV, but despite excellent effectiveness the failures still occur. The aim of our study was to evaluate the efficacy of retreatment with genotype specific direct acting antivirals- (DAA-) based regimens in nonresponders to previous IFN-free therapy. Materials and Methods. Analysed population consisted of 31 nonresponders to IFN-free regimen, which received second IFN-free rescue therapy, selected from 6228 patients included in a national database EpiTer-2. Results. Age and gender distribution were similar, whereas proportion of genotype lb was slightly higher and genotype 4 lower in the whole population compared to studied one. Patients included in the study demonstrated much more advanced fibrosis. Primary therapy was discontinued in 12 patients, which were recognized as failures due to nonvirologic reason, whereas virologic reason of therapeutic failure was recognized in 19 patients which completed therapy. Overall sustained virologic response (SVR) rate was 81% and 86% in intent-to-treat (ITT) and modified ITT analysis, respectively (74% and 78% in virologic failures, 92% and 100% in nonvirologic failures). Resistance-associated substitutions (RAS) testing was carried out in 8 patients from the group of completed primary therapy and three of them had potential risk for failure of rescue therapy due to NS5A association, while two of them achieved SVR. Conclusions. We demonstrated moderate effectiveness of genotype specific rescue therapy in failures due to virologic reason and high in those who discontinued primary therapy. Therefore rescue therapy with genotype specific regimens should be considered always if more potent regimens are not available.
机译:背景和目标。无干扰素(IFN)方案的开发极大地提高了丙型肝炎的治疗效果,但尽管效果很好,但失败仍然存在。我们研究的目的是评估基因型特异性直接作用抗病毒药物(DAA)为基础的治疗方案对既往无干扰素治疗无反应者的再治疗效果。材料和方法。分析人群包括31名对无干扰素方案无反应的患者,这些患者接受了第二次无干扰素抢救治疗,这些患者选自国家数据库EpiTer-2中的6228名患者。后果年龄和性别分布相似,而与研究人群相比,在整个人群中,基因型lb的比例略高,基因型4的比例更低。参与研究的患者表现出更为严重的纤维化。12名患者中断了初级治疗,这些患者被认为是由于非病毒学原因导致的治疗失败,而19名完成治疗的患者被认为是病毒学原因导致的治疗失败。意向治疗(ITT)和改良ITT分析的总体持续病毒学应答(SVR)率分别为81%和86%(病毒学失败为74%和78%,非病毒学失败为92%和100%)。在完成初级治疗组的8名患者中进行了耐药性相关替代(RAS)测试,其中3名患者由于NS5A关联而存在抢救治疗失败的潜在风险,而其中2名患者实现了SVR。结论。我们证明了基因型特异性抢救治疗在因病毒学原因而失败的患者中的中度有效性,而在停止原发性治疗的患者中的有效性较高。因此,如果没有更有效的方案,应始终考虑使用基因型特异性方案进行抢救治疗。

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