Role of ledipasvir/sofosbuvir combination for genotype 1 hepatitis C virus infection

Vinay Sundaram,1 Kris V Kowdley21Department of Medicine and Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, 2Liver Care Network, Swedish Medical Center, Seattle, WA, USAAbstract: Chronic hepatitis C virus (HCV) infection is one of the most common etiologies of liver-re...

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Autores principales: Sundaram V, Kowdley KV
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Publicado: Dove Medical Press 2016
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spelling oai:doaj.org-article:ba5f8beb2510482eb17737c373e193642021-12-02T00:51:38ZRole of ledipasvir/sofosbuvir combination for genotype 1 hepatitis C virus infection1179-1535https://doaj.org/article/ba5f8beb2510482eb17737c373e193642016-06-01T00:00:00Zhttps://www.dovepress.com/role-of-ledipasvirsofosbuvir-combination-for-genotype-1-hepatitis-c-vi-peer-reviewed-article-HMERhttps://doaj.org/toc/1179-1535Vinay Sundaram,1 Kris V Kowdley21Department of Medicine and Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, 2Liver Care Network, Swedish Medical Center, Seattle, WA, USAAbstract: Chronic hepatitis C virus (HCV) infection is one of the most common etiologies of liver-related mortality throughout the world. Among the six HCV genotypes, genotype 1 was significantly more aggressive when utilizing the combination of pegylated interferon and ribavirin, as genotype 1-infected patients had the lowest likelihood of achieving cure (40%–50%) and required twice as long duration of treatment, as compared to genotypes 2 and 3. Recently, however, significant advances have been made with the advent of all-oral direct-acting antiviral agents, which have significantly improved the safety, efficacy, and tolerability of the treatment of HCV genotype 1. Among the available treatments for HCV genotype 1, the combination therapy of ledipasvir/sofosbuvir provides several advantages compared to other regimens, including use of a single-pill regimen, possibility to shorten the duration of treatment to 8 weeks, efficacy in patients exposed to protease inhibitors, safety in decompensated cirrhosis, and potential to avoid ribavirin. In this review, we discuss the pharmacotherapy of the combination of ledipasvir/sofosbuvir therapy and summarize the results of the Phase III clinical trials for this treatment in HCV genotype 1 patients. We will also discuss the data for special populations, including decompensated cirrhosis, human immunodeficiency virus (HIV) coinfected patients, African-Americans, the elderly, and those who failed sofosbuvir-containing regimens.Keywords: pegylated interferon, ribavirin, cirrhosis, liver transplantation, direct-acting antiviralSundaram VKowdley KVDove Medical Pressarticlepegylated interferonribaviringenotype 1direct acting antiviralDiseases of the digestive system. GastroenterologyRC799-869ENHepatic Medicine: Evidence and Research, Vol 2016, Iss Issue 1, Pp 75-80 (2016)
institution DOAJ
collection DOAJ
language EN
topic pegylated interferon
ribavirin
genotype 1
direct acting antiviral
Diseases of the digestive system. Gastroenterology
RC799-869
spellingShingle pegylated interferon
ribavirin
genotype 1
direct acting antiviral
Diseases of the digestive system. Gastroenterology
RC799-869
Sundaram V
Kowdley KV
Role of ledipasvir/sofosbuvir combination for genotype 1 hepatitis C virus infection
description Vinay Sundaram,1 Kris V Kowdley21Department of Medicine and Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, CA, 2Liver Care Network, Swedish Medical Center, Seattle, WA, USAAbstract: Chronic hepatitis C virus (HCV) infection is one of the most common etiologies of liver-related mortality throughout the world. Among the six HCV genotypes, genotype 1 was significantly more aggressive when utilizing the combination of pegylated interferon and ribavirin, as genotype 1-infected patients had the lowest likelihood of achieving cure (40%–50%) and required twice as long duration of treatment, as compared to genotypes 2 and 3. Recently, however, significant advances have been made with the advent of all-oral direct-acting antiviral agents, which have significantly improved the safety, efficacy, and tolerability of the treatment of HCV genotype 1. Among the available treatments for HCV genotype 1, the combination therapy of ledipasvir/sofosbuvir provides several advantages compared to other regimens, including use of a single-pill regimen, possibility to shorten the duration of treatment to 8 weeks, efficacy in patients exposed to protease inhibitors, safety in decompensated cirrhosis, and potential to avoid ribavirin. In this review, we discuss the pharmacotherapy of the combination of ledipasvir/sofosbuvir therapy and summarize the results of the Phase III clinical trials for this treatment in HCV genotype 1 patients. We will also discuss the data for special populations, including decompensated cirrhosis, human immunodeficiency virus (HIV) coinfected patients, African-Americans, the elderly, and those who failed sofosbuvir-containing regimens.Keywords: pegylated interferon, ribavirin, cirrhosis, liver transplantation, direct-acting antiviral
format article
author Sundaram V
Kowdley KV
author_facet Sundaram V
Kowdley KV
author_sort Sundaram V
title Role of ledipasvir/sofosbuvir combination for genotype 1 hepatitis C virus infection
title_short Role of ledipasvir/sofosbuvir combination for genotype 1 hepatitis C virus infection
title_full Role of ledipasvir/sofosbuvir combination for genotype 1 hepatitis C virus infection
title_fullStr Role of ledipasvir/sofosbuvir combination for genotype 1 hepatitis C virus infection
title_full_unstemmed Role of ledipasvir/sofosbuvir combination for genotype 1 hepatitis C virus infection
title_sort role of ledipasvir/sofosbuvir combination for genotype 1 hepatitis c virus infection
publisher Dove Medical Press
publishDate 2016
url https://doaj.org/article/ba5f8beb2510482eb17737c373e19364
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