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西班牙 GEHEP-004 队列研究中,耐药相关替代与基线耐药指导的慢性丙型肝炎治疗疗效的相关性。

Prevalence of resistance associated substitutions and efficacy of baseline resistance-guided chronic hepatitis C treatment in Spain from the GEHEP-004 cohort.

机构信息

Clinical Microbiology Unit, University Hospital Reina Sofía, Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Córdoba, Spain.

Clinical Microbiology Unit, University Hospital San Cecilio, Instituto de Investigacion Ibs. Granada, Granada, Spain.

出版信息

PLoS One. 2019 Aug 30;14(8):e0221231. doi: 10.1371/journal.pone.0221231. eCollection 2019.

Abstract

Treatment guidelines differ in their recommendation to determine baseline resistance associated substitutions (RAS) before starting a first-line treatment with direct-acting antivirals (DAAs). Here we analyze the efficacy of DAA treatment with baseline RAS information. We conducted a prospective study involving 23 centers collaborating in the GEHEP-004 DAA resistance cohort. Baseline NS5A and NS3 RASs were studied by Sanger sequencing. After issuing a comprehensive resistance report, the treating physician decided the therapy, duration and ribavirin use. Sustained virological response (SVR12) data are available in 275 patients. Baseline NS5A RAS prevalence was between 4.3% and 26.8% according to genotype, and NS3 RASs prevalence (GT1a) was 6.3%. Overall, SVR12 was 97.8%. Amongst HCV-GT1a patients, 75.0% had >800,000 IU/ml and most of those that started grazoprevir/elbasvir were treated for 12 weeks. In genotype 3, NS5A Y93H was detected in 9 patients. 42.8% of the HCV-GT3 patients that started sofosbuvir/velpatasvir included ribavirin, although only 14.7% carried Y93H. The efficacy of baseline resistance-guided treatment in our cohort has been high across the most prevalent HCV genotypes in Spain. The duration of the grazoprevir/elbasvir treatment adhered mostly to AASLD/IDSA recommendations. In cirrhotic patients infected with GT-3 there has been a high use of ribavirin.

摘要

治疗指南在推荐使用直接作用抗病毒药物(DAA)进行一线治疗之前,确定基线耐药相关替代(RAS)方面存在差异。在此,我们分析了具有基线 RAS 信息的 DAA 治疗效果。我们进行了一项前瞻性研究,涉及到 23 个合作参与 GEHEP-004 DAA 耐药队列的中心。通过 Sanger 测序研究了基线 NS5A 和 NS3 RAS。在发布全面耐药报告后,主治医生决定治疗方案、持续时间和利巴韦林的使用。在 275 名患者中获得了持续病毒学应答(SVR12)数据。根据基因型,基线 NS5A RAS 的流行率在 4.3%至 26.8%之间,而 NS3 RAS 流行率(GT1a)为 6.3%。总体而言,SVR12 为 97.8%。在 HCV-GT1a 患者中,75.0%的病毒载量超过 800,000 IU/ml,且大多数接受格拉替雷韦/艾尔巴韦尔治疗的患者治疗时间为 12 周。在基因型 3 中,检测到 9 例 NS5A Y93H。在开始使用索磷布韦/维帕他韦治疗的 HCV-GT3 患者中,有 42.8%包括利巴韦林,尽管只有 14.7%的患者携带 Y93H。在我们的队列中,根据基线耐药指导的治疗在西班牙最常见的 HCV 基因型中效果良好。格拉替雷韦/艾尔巴韦尔治疗的持续时间大多符合 AASLD/IDSA 建议。在感染 GT-3 的肝硬化患者中,利巴韦林的使用量很高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f4d/6716636/24c0e98a4926/pone.0221231.g001.jpg

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