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Hepatitis C virus treatment failure: Clinical utility for testing resistance-associated substitutions
The hepatitis C virus has a high mutation capacity that leads to the emergence of resistance-associated substitutions (RAS). However, the consequence of resistance selection during new direct-acting antiviral drug (DAA) treatment is not necessarily the therapeutic failure. In fact, DAA treatment has...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473504/ https://www.ncbi.nlm.nih.gov/pubmed/34630875 http://dx.doi.org/10.4254/wjh.v13.i9.1069 |
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author | Ridruejo, Ezequiel Pereson, Matías Javier Flichman, Diego M Di Lello, Federico Alejandro |
author_facet | Ridruejo, Ezequiel Pereson, Matías Javier Flichman, Diego M Di Lello, Federico Alejandro |
author_sort | Ridruejo, Ezequiel |
collection | PubMed |
description | The hepatitis C virus has a high mutation capacity that leads to the emergence of resistance-associated substitutions (RAS). However, the consequence of resistance selection during new direct-acting antiviral drug (DAA) treatment is not necessarily the therapeutic failure. In fact, DAA treatment has shown a high rate (> 95%) of sustained virological response even when high baseline RAS prevalence has been reported. In the context of RAS emergence and high rates of sustained viral response, the clinical relevance of variants harboring RAS is still controversial. Therefore, in order to summarize the data available in international guidelines, we have reviewed the clinical utility of testing RAS in the era of new pangenotypic DAA drugs. |
format | Online Article Text |
id | pubmed-8473504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-84735042021-10-08 Hepatitis C virus treatment failure: Clinical utility for testing resistance-associated substitutions Ridruejo, Ezequiel Pereson, Matías Javier Flichman, Diego M Di Lello, Federico Alejandro World J Hepatol Minireviews The hepatitis C virus has a high mutation capacity that leads to the emergence of resistance-associated substitutions (RAS). However, the consequence of resistance selection during new direct-acting antiviral drug (DAA) treatment is not necessarily the therapeutic failure. In fact, DAA treatment has shown a high rate (> 95%) of sustained virological response even when high baseline RAS prevalence has been reported. In the context of RAS emergence and high rates of sustained viral response, the clinical relevance of variants harboring RAS is still controversial. Therefore, in order to summarize the data available in international guidelines, we have reviewed the clinical utility of testing RAS in the era of new pangenotypic DAA drugs. Baishideng Publishing Group Inc 2021-09-27 2021-09-27 /pmc/articles/PMC8473504/ /pubmed/34630875 http://dx.doi.org/10.4254/wjh.v13.i9.1069 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Minireviews Ridruejo, Ezequiel Pereson, Matías Javier Flichman, Diego M Di Lello, Federico Alejandro Hepatitis C virus treatment failure: Clinical utility for testing resistance-associated substitutions |
title | Hepatitis C virus treatment failure: Clinical utility for testing resistance-associated substitutions |
title_full | Hepatitis C virus treatment failure: Clinical utility for testing resistance-associated substitutions |
title_fullStr | Hepatitis C virus treatment failure: Clinical utility for testing resistance-associated substitutions |
title_full_unstemmed | Hepatitis C virus treatment failure: Clinical utility for testing resistance-associated substitutions |
title_short | Hepatitis C virus treatment failure: Clinical utility for testing resistance-associated substitutions |
title_sort | hepatitis c virus treatment failure: clinical utility for testing resistance-associated substitutions |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473504/ https://www.ncbi.nlm.nih.gov/pubmed/34630875 http://dx.doi.org/10.4254/wjh.v13.i9.1069 |
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