Treatment-Resistant Hepatitis C Viral Infection: A Case Report and Literature Review.

Case Reports in Hepatology Pub Date : 2022-03-11 eCollection Date: 2022-01-01 DOI:10.1155/2022/3556780
Victoria Green, Marina Roytman
{"title":"Treatment-Resistant Hepatitis C Viral Infection: A Case Report and Literature Review.","authors":"Victoria Green,&nbsp;Marina Roytman","doi":"10.1155/2022/3556780","DOIUrl":null,"url":null,"abstract":"<p><p>Hepatitis C virus (HCV) is an ongoing global public health threat affecting millions worldwide. Increasing recognition of its impact and recent advances towards HCV prevention and cure have provided incentive for the World Health Organization to call for global elimination by 2030. The goal of therapy is to achieve a sustained virologic response (SVR-12), defined as undetectable HCV-RNA within 12 weeks after treatment completion. In 2011, approval was given for the first direct-acting antiviral agents (DAAs). More recently, in 2013, more effective DAAs, with pan-genomic properties, have been introduced, and these regimens boast increasing rates of SVR. The ultimate goal is that the history of HCV ends with the pan-genotypic efficacy of multiple, easy-to-use and tolerate, combination regimens. These regimens have already demonstrated the ability to cure previously challenging patient groups. However, limitations exist in the current portfolio of agents, with suboptimal outcomes for patients with HCV genotype 3. In addition to this, access to DAAs remains an obstacle for many patients. We present this case of a 61-year-old male with HCV genotype 3 who has had several treatment failures with standard HCV therapy who was eventually approved for compassionate use of a 16-week course of glecaprevir (GLE)/pibrentasvir (PIB), sofosbuvir (SOF), and ribavirin (RBV) which ultimately led to SVR-12.</p>","PeriodicalId":30295,"journal":{"name":"Case Reports in Hepatology","volume":" ","pages":"3556780"},"PeriodicalIF":0.0000,"publicationDate":"2022-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933098/pdf/","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Reports in Hepatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2022/3556780","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Hepatitis C virus (HCV) is an ongoing global public health threat affecting millions worldwide. Increasing recognition of its impact and recent advances towards HCV prevention and cure have provided incentive for the World Health Organization to call for global elimination by 2030. The goal of therapy is to achieve a sustained virologic response (SVR-12), defined as undetectable HCV-RNA within 12 weeks after treatment completion. In 2011, approval was given for the first direct-acting antiviral agents (DAAs). More recently, in 2013, more effective DAAs, with pan-genomic properties, have been introduced, and these regimens boast increasing rates of SVR. The ultimate goal is that the history of HCV ends with the pan-genotypic efficacy of multiple, easy-to-use and tolerate, combination regimens. These regimens have already demonstrated the ability to cure previously challenging patient groups. However, limitations exist in the current portfolio of agents, with suboptimal outcomes for patients with HCV genotype 3. In addition to this, access to DAAs remains an obstacle for many patients. We present this case of a 61-year-old male with HCV genotype 3 who has had several treatment failures with standard HCV therapy who was eventually approved for compassionate use of a 16-week course of glecaprevir (GLE)/pibrentasvir (PIB), sofosbuvir (SOF), and ribavirin (RBV) which ultimately led to SVR-12.

难治性丙型肝炎病毒感染1例报告及文献复习。
丙型肝炎病毒(HCV)是一种持续的全球公共卫生威胁,影响全世界数百万人。人们日益认识到其影响以及最近在预防和治疗丙肝病毒方面取得的进展,促使世界卫生组织呼吁到2030年在全球消除丙肝病毒。治疗的目标是实现持续病毒学应答(SVR-12),定义为在治疗完成后12周内检测不到HCV-RNA。2011年,首个直接作用抗病毒药物(DAAs)获得批准。最近,在2013年,引入了更有效的daa,具有泛基因组特性,这些方案以增加SVR率而闻名。最终目标是使HCV的历史结束于多种、易于使用和耐受的联合治疗方案的泛基因型疗效。这些方案已经证明能够治愈以前具有挑战性的患者群体。然而,目前的药物组合存在局限性,对于HCV基因型3的患者,结果不理想。除此之外,获得DAAs仍然是许多患者的障碍。我们报告了一名61岁的HCV基因型3型男性患者,他曾多次接受标准HCV治疗失败,最终被批准使用16周疗程的glecaprevir (GLE)/pibrentasvir (PIB),索非布韦(SOF)和利巴韦林(RBV),最终导致SVR-12。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
12
审稿时长
12 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信