Baseline hepatitis C virus resistance-associated substitutions present at frequencies lower than 15% may be clinically significant

dc.contributor.authorPerales, Celia
dc.contributor.authorChen, Qian
dc.contributor.authorSoria, Maria Eugenia
dc.contributor.authorGregori, Josep
dc.contributor.authorGarcia Cehic, Damir
dc.contributor.authorNieto Aponte, Leonardo
dc.contributor.authorCastells, Lluis
dc.contributor.authorImaz, Arkaitz
dc.contributor.authorLlorens Revull, Meritxell
dc.contributor.authorDomingo, Esteban
dc.contributor.authorButi, Maria
dc.contributor.authorEsteban, Juan Ignacio
dc.contributor.authorRodríguez-Frías, Francisco
dc.contributor.authorQuer, Josep
dc.date.accessioned2020-12-09T19:08:18Z
dc.date.available2020-12-09T19:08:18Z
dc.date.issued2018-01-01
dc.date.updated2020-12-02T16:26:59Z
dc.description.abstractBackground: Controversy is ongoing about whether a minority mutant present at frequencies below 15% may be clinically relevant and should be considered to guide treatment. Methods: Resistance-associated substitution (RAS) studies were performed in patients before and at failure of antiviral treatments using Next-generation hepatitis C virus (HCV) sequencing (NGS). Results: We have found two patients with genotype 1a infection having RAS in 3.5%-7.1% of the viral population at baseline that were selected during ledipasvir + sofosbuvir treatment. Coselection of RAS located in a region not directly affected by the antiviral treatment also occurred. This observation calls into question, the recommendations to guide RAS-based direct-acting antiviral (DAA) treatment only when RAS are present in > 15% of the sequences generated. Conclusion: Our results suggests that RAS study should include all three HCV DAA target proteins and minority mutants should be considered as clinically relevant.
dc.format.extent4 p.
dc.format.mimetypeapplication/pdf
dc.identifier.pmid30519058
dc.identifier.urihttps://hdl.handle.net/2445/172632
dc.language.isoeng
dc.publisherDove Medical Press Ltd.
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.2147/IDR.S172226
dc.relation.ispartofInfection and Drug Resistance, 2018, vol. 11, p. 2207-2210
dc.relation.urihttps://doi.org/10.2147/IDR.S172226
dc.rightscc by-nc (c) Perales et al., 2018
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationHepatitis C
dc.subject.classificationMedicaments antivírics
dc.subject.otherHepatitis C
dc.subject.otherAntiviral agents
dc.titleBaseline hepatitis C virus resistance-associated substitutions present at frequencies lower than 15% may be clinically significant
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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