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Using pegylated interferon alfa-2b and ribavirin to treat chronic hepatitis patients infected with hepatitis C virus genotype 1: Are nonresponders and relapsers different populations?

dc.contributor.authorSilva, Giovanni Faria [UNESP]
dc.contributor.authorPolonio, Rodrigo Jose [UNESP]
dc.contributor.authorPardini, Maria Ines de Moura Campos [UNESP]
dc.contributor.authorCorvino, Silvia Maria
dc.contributor.authorSaccomano Henriques, Rita Maria
dc.contributor.authorPeres, Mari Nilce [UNESP]
dc.contributor.authorSilveira, Liciana Vaz de Arruda [UNESP]
dc.contributor.authorCoelho, Kunie Iabuki Rabello [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T15:20:34Z
dc.date.available2014-05-20T15:20:34Z
dc.date.issued2007-12-01
dc.description.abstractThe combination of pegylated interferon (PEG-INF) and ribavirin is currently the best treatment for chronic hepatitis C, providing a sustained virological response (SVR) in 54%-63% of patients. In patients infected with hepatitis C virus (HCV) genotype 1, the SVR rate is 42%-52%. To evaluate the treatment efficacy of this drug combination, we conducted an open, prospective study of 58 consecutive treatment-naive patients infected with HCV genotype 1 and treated at a university hospital, comparing those presenting an SVR (SVRs), nonresponders (NRs), and relapsers (RELs). Among the intent-to-treat patients, an end-of-treatment virological response was achieved in 69 % of the sample as a whole and in 52 % of the SVRs. We found that being an SVR was significantly associated with mild fibrosis (p = 0.04) and with undetectable HCV RNA at weeks 12 and 24 of treatment (p < 0.0001). Comparing the SVR and REL groups, we observed that being older than 40 was significantly associated with being a REL (p = 0.04). Being an NR was found to be associated with severe fibrosis and moderate inflammatory infiltrates (portal or periportal). In the polytomous logistic regression, no independent factors were associated with the REL group when compared with the SVR group. We conclude that RELs and NRs differ in comparison with SVRs. The RELs accounted for 17% of the sample. The HCV RNA test results at weeks 12 and 24 of treatment, although independent predictors of non-response (OR: 4.8 and 8.2, respectively), did not differ between SVRs and RELs.en
dc.description.affiliationUNESP, Fac Med Botucatu, Dept Internal Med, BR-18618000 Botucatu, SP, Brazil
dc.description.affiliationHemoctr Botucatu, Virol Lab, Botucatu, SP, Brazil
dc.description.affiliationDept Pathol, Botucatu, SP, Brazil
dc.description.affiliationUnespUNESP, Fac Med Botucatu, Dept Internal Med, BR-18618000 Botucatu, SP, Brazil
dc.format.extent554-560
dc.identifierhttp://dx.doi.org/10.1590/S1413-86702007000600006
dc.identifier.citationBrazilian Journal of Infectious Diseases. Salvador: Contexto, v. 11, n. 6, p. 554-560, 2007.
dc.identifier.doi10.1590/S1413-86702007000600006
dc.identifier.fileWOS000254388800006.pdf
dc.identifier.issn1413-8670
dc.identifier.lattes6322604200510676
dc.identifier.lattes7805298466001457
dc.identifier.lattes4619588334582084
dc.identifier.scieloS1413-86702007000600006
dc.identifier.urihttp://hdl.handle.net/11449/31840
dc.identifier.wosWOS:000254388800006
dc.language.isoeng
dc.publisherContexto
dc.relation.ispartofBrazilian Journal of Infectious Diseases
dc.relation.ispartofjcr2.083
dc.relation.ispartofsjr0,817
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjecthepatitis Cpt
dc.subjectpegylated interferon alfa 2bpt
dc.subjectgenotype 1pt
dc.subjectrelapserspt
dc.titleUsing pegylated interferon alfa-2b and ribavirin to treat chronic hepatitis patients infected with hepatitis C virus genotype 1: Are nonresponders and relapsers different populations?en
dc.typeArtigo
dcterms.licensehttp://www.scielo.br/revistas/bjid/iaboutj.htm
dcterms.rightsHolderContexto
dspace.entity.typePublication
unesp.author.lattes6322604200510676
unesp.author.lattes7805298466001457[8]
unesp.author.lattes4619588334582084
unesp.author.orcid0000-0001-8931-5495[7]
unesp.author.orcid0000-0001-8931-5495[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina, Botucatupt
unesp.departmentClínica Médica - FMBpt

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