Malespin Miguel, Benyashvili Tamara, Uprichard Susan L, Perelson Alan S, Dahari Harel, Cotler Scott J
Division of Gastroenterology and Hepatology, Department of Medicine, University of Florida Health, 4555 Emerson St. Ste. 300, Jacksonville, FL 32207, USA.
Program for Experimental and Theoretical Modeling, Division of Hepatology, Department of Medicine, Loyola University Medical Center, Maywood, IL, USA.
Therap Adv Gastroenterol. 2017 Jan;10(1):68-73. doi: 10.1177/1756283X16672392. Epub 2016 Oct 17.
Some chronic hepatitis C virus (HCV), genotype 1 infected patients treated with direct antiviral agents (DAAs) remain viremic at end of treatment (EOT+), yet go on to achieve sustained virological response 12 weeks after completion of therapy (SVR). The incidence of EOT+/SVR in patients with genotype 1 and other genotypes, as well as whether such patients achieve SVR remain in question. The aims of this study were to evaluate the frequency and durability of EOT+/SVR and other response categories in HCV genotype 1, 2, or 3 infected patients treated with DAA in clinical practice.
Data from patients treated with all oral sofosbuvir-based regimens at a university hepatology practice by 1 July 2015 were reviewed retrospectively. Responses were categorized based on virus levels during and post DAA treatment. HCV RNA levels were measured by Abbott RealTime HCV (ART) or by Roche CobasTaqMan v2.0 (RCTM) assays.
The study population included 89 patients. Participants were 62% genotype 1, 19% genotype 2 and 19% genotype 3, 54% cirrhotic and 46% treatment-experienced. A total of 45 received sofosbuvir-simeprevir, 38 sofosbuvir-ribavirin and 6 sofosbuvir-ledipasvir. The SVR rate was 82%. A total of 5 patients (6%), all with genotype 1, had EOT+ by ART assay and each achieved SVR.
A total of 9% of genotype 1 patients (6% overall) treated with DAAs were EOT+ by ART and all EOT+ cases achieved SVR. EOT+/SVR was not observed with genotype 2 or 3 or by the RCTM assay. In patients treated with DAAs, EOT+ by the ART assay does not indicate treatment failure.
一些接受直接抗病毒药物(DAA)治疗的慢性丙型肝炎病毒(HCV)1型感染患者在治疗结束时(EOT+)仍有病毒血症,但在治疗完成后12周实现了持续病毒学应答(SVR)。1型及其他基因型患者中EOT+/SVR的发生率以及此类患者是否能实现SVR仍存在疑问。本研究的目的是评估在临床实践中接受DAA治疗的HCV 1、2或3型感染患者中EOT+/SVR及其他应答类别出现的频率和持久性。
回顾性分析2015年7月1日前在一所大学肝病科接受基于索磷布韦的全口服方案治疗的患者数据。根据DAA治疗期间及之后的病毒水平对应答进行分类。HCV RNA水平通过雅培实时HCV(ART)或罗氏Cobas TaqMan v2.0(RCTM)检测法进行测定。
研究人群包括89名患者。参与者中62%为1型,19%为2型,19%为3型,54%为肝硬化患者,46%有治疗史。共有45人接受索磷布韦-西米普明治疗,38人接受索磷布韦-利巴韦林治疗,6人接受索磷布韦-来迪帕司韦治疗。SVR率为82%。共有5名患者(6%),均为1型,通过ART检测法在EOT时仍有病毒血症,且均实现了SVR。
接受DAA治疗的1型患者中共有9%(总体为6%)通过ART检测法在EOT时仍有病毒血症,且所有EOT+病例均实现了SVR。2型或3型患者或通过RCTM检测法未观察到EOT+/SVR。在接受DAA治疗的患者中,通过ART检测法出现EOT+并不表明治疗失败。