Literature DB >> 34967486

Road to elimination of HCV: Clinical challenges in HCV management.

C Nelson Hayes1,2, Michio Imamura1,2, Junko Tanaka2,3, Kazuaki Chayama2,4,5.   

Abstract

Since its discovery in 1989, the road to a cure for hepatitis C virus (HCV) has been slow, but most patients can now expect to achieve a sustained virological response (SVR). With direct-acting antiviral (DAA) combination therapies such as glecaprevir/pibrentasvir and velpatasvir/sofosbuvir, 98% of patients successfully eradicate the virus, even if previous treatments failed or if resistance-associated substitutions (RASs) are present. Adverse events are rare or mild, and patients with compensated cirrhosis and other co-morbidities are often eligible for treatment. However, a small number of patients fail to eradicate the virus even after retreatment. The cause of failure is mainly due to emergence of NS5A P32 deletion mutants after initial DAA therapy in genotype 1b patients, although the reason is unknown for some patients. Alternative therapies that do not rely on NS5A inhibitors, such as sofosbuvir plus ribavirin, can be attempted in these patients. While scaled-up treatment efforts present a challenge, another problem is that many carriers are unaware of their infection. Long-term damage to the liver becomes irreversible, and patients who are not diagnosed in time can develop liver cancer or liver failure even after eliminating the virus. The long-term costs of treatment of advanced liver disease in undiagnosed patients relative to the immediate costs of DAA therapy should be considered. As no vaccine is yet available, eventual elimination of the virus requires identifying and treating undiagnosed cases and screening of high-risk populations such as injection drug users and men who have sex with men and female sex workers.
© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  P32 deletion; direct-acting antivirals; glecaprevir/pibrentasvir; sustained virological response; velpatasvir/sofosbuvir

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Substances:

Year:  2022        PMID: 34967486     DOI: 10.1111/liv.15150

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   8.754


  4 in total

1.  Synergistic inhibition of hepatitis C virus infection by a novel microtubule inhibitor in combination with daclatasvir.

Authors:  Huijun Zhang; Xing-Quan Zhang; Lina S Huang; Xiong Fang; Mohsin Khan; Yan Xu; Jing An; Robert T Schooley; Ziwei Huang
Journal:  Biochem Biophys Rep       Date:  2022-05-24

2.  Very low levels of remdesivir resistance in SARS-COV-2 genomes after 18 months of massive usage during the COVID19 pandemic: A GISAID exploratory analysis.

Authors:  Daniele Focosi; Fabrizio Maggi; Scott McConnell; Arturo Casadevall
Journal:  Antiviral Res       Date:  2022-01-13       Impact factor: 5.970

3.  Modeling-Based Response-Guided DAA Therapy for Chronic Hepatitis C to Identify Individuals for Shortening Treatment Duration.

Authors:  Ashish Goyal; Alex Churkin; Danny Barash; Scott J Cotler; Amir Shlomai; Ohad Etzion; Harel Dahari
Journal:  Open Forum Infect Dis       Date:  2022-03-22       Impact factor: 4.423

4.  Mathematical modeling of plus-strand RNA virus replication to identify broad-spectrum antiviral treatment strategies.

Authors:  Carolin Zitzmann; Christopher Dächert; Bianca Schmid; Hilde van der Schaar; Martijn van Hemert; Alan S Perelson; Frank J M van Kuppeveld; Ralf Bartenschlager; Marco Binder; Lars Kaderali
Journal:  bioRxiv       Date:  2022-07-25
  4 in total

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