Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study

Detalhes bibliográficos
Autor(a) principal: Silva,Giovanni Faria
Data de Publicação: 2014
Outros Autores: Villela-Nogueira,Cristiane A., Brandão Mello,Carlos Eduardo, Soares,Elza Cotrim, Coelho,Henrique Sergio M., Abrão Ferreira,Paulo Roberto, Ruiz,Fernando José Goes
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Infectious Diseases
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702014000100048
Resumo: Background:Tolerance and response to antiviral HCV treatment is poor in advanced fibrosis. The aim of this study was to assess SVR rate and its predictive factors in HCV advanced fibrosis patients treated in real life with full dose PEG-IFN plus RBV and to evaluate the adverse events related to treatment.Methods:A multicentric, retrospective study was conducted at six university hospitals. METAVIR F3 and F4 HCV monoinfected patients who were treated with PEG-IFN and RBV had their data analyzed. A stepwise logistic regression analysis was performed to identify the variables independently related to SVR. Adverse events were recorded during treatment.Results:308 patients were included, 75% genotype 1 and 23% genotype 3. METAVIR F3 was present in 39% and F4 in 61% of patients. The median Child Pugh score for F4 patients was 5 (5–9). The global SVR rate was 34%, 11% were relapsers and 55% were nonresponders. SVR rates were similar between patients treated with PEG-IFN alfa 2a or alfa 2b (p = 0.24). SVR rates according to Child–Pugh score were 26% (Child A) and 18% (Child B). The independent factors related to SVR in F4 patients were genotype 3, RVR and fewer Child Pugh score points. Treatment interruption occurred in 31% patients and death occurred in 1.9%, all with liver cirrhosis.Conclusion:Treatment of HCV in patients with advanced fibrosis should not be postponed. However, a very careful evaluation of cirrhotic patients must be performed before treatment is indicated and careful monitoring is required during treatment.
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spelling Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life studyHepatitis CAdvanced fibrosisPeginterferonRibavirinBackground:Tolerance and response to antiviral HCV treatment is poor in advanced fibrosis. The aim of this study was to assess SVR rate and its predictive factors in HCV advanced fibrosis patients treated in real life with full dose PEG-IFN plus RBV and to evaluate the adverse events related to treatment.Methods:A multicentric, retrospective study was conducted at six university hospitals. METAVIR F3 and F4 HCV monoinfected patients who were treated with PEG-IFN and RBV had their data analyzed. A stepwise logistic regression analysis was performed to identify the variables independently related to SVR. Adverse events were recorded during treatment.Results:308 patients were included, 75% genotype 1 and 23% genotype 3. METAVIR F3 was present in 39% and F4 in 61% of patients. The median Child Pugh score for F4 patients was 5 (5–9). The global SVR rate was 34%, 11% were relapsers and 55% were nonresponders. SVR rates were similar between patients treated with PEG-IFN alfa 2a or alfa 2b (p = 0.24). SVR rates according to Child–Pugh score were 26% (Child A) and 18% (Child B). The independent factors related to SVR in F4 patients were genotype 3, RVR and fewer Child Pugh score points. Treatment interruption occurred in 31% patients and death occurred in 1.9%, all with liver cirrhosis.Conclusion:Treatment of HCV in patients with advanced fibrosis should not be postponed. However, a very careful evaluation of cirrhotic patients must be performed before treatment is indicated and careful monitoring is required during treatment.Brazilian Society of Infectious Diseases2014-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702014000100048Brazilian Journal of Infectious Diseases v.18 n.1 2014reponame:Brazilian Journal of Infectious Diseasesinstname:Brazilian Society of Infectious Diseases (BSID)instacron:BSID10.1016/j.bjid.2013.05.007info:eu-repo/semantics/openAccessSilva,Giovanni FariaVillela-Nogueira,Cristiane A.Brandão Mello,Carlos EduardoSoares,Elza CotrimCoelho,Henrique Sergio M.Abrão Ferreira,Paulo RobertoRuiz,Fernando José Goeseng2015-08-28T00:00:00Zoai:scielo:S1413-86702014000100048Revistahttps://www.bjid.org.br/https://old.scielo.br/oai/scielo-oai.phpbjid@bjid.org.br||lgoldani@ufrgs.br1678-43911413-8670opendoar:2015-08-28T00:00Brazilian Journal of Infectious Diseases - Brazilian Society of Infectious Diseases (BSID)false
dc.title.none.fl_str_mv Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study
title Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study
spellingShingle Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study
Silva,Giovanni Faria
Hepatitis C
Advanced fibrosis
Peginterferon
Ribavirin
title_short Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study
title_full Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study
title_fullStr Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study
title_full_unstemmed Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study
title_sort Peginterferon plus ribavirin and sustained virological response rate in HCV-related advanced fibrosis: a real life study
author Silva,Giovanni Faria
author_facet Silva,Giovanni Faria
Villela-Nogueira,Cristiane A.
Brandão Mello,Carlos Eduardo
Soares,Elza Cotrim
Coelho,Henrique Sergio M.
Abrão Ferreira,Paulo Roberto
Ruiz,Fernando José Goes
author_role author
author2 Villela-Nogueira,Cristiane A.
Brandão Mello,Carlos Eduardo
Soares,Elza Cotrim
Coelho,Henrique Sergio M.
Abrão Ferreira,Paulo Roberto
Ruiz,Fernando José Goes
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Silva,Giovanni Faria
Villela-Nogueira,Cristiane A.
Brandão Mello,Carlos Eduardo
Soares,Elza Cotrim
Coelho,Henrique Sergio M.
Abrão Ferreira,Paulo Roberto
Ruiz,Fernando José Goes
dc.subject.por.fl_str_mv Hepatitis C
Advanced fibrosis
Peginterferon
Ribavirin
topic Hepatitis C
Advanced fibrosis
Peginterferon
Ribavirin
description Background:Tolerance and response to antiviral HCV treatment is poor in advanced fibrosis. The aim of this study was to assess SVR rate and its predictive factors in HCV advanced fibrosis patients treated in real life with full dose PEG-IFN plus RBV and to evaluate the adverse events related to treatment.Methods:A multicentric, retrospective study was conducted at six university hospitals. METAVIR F3 and F4 HCV monoinfected patients who were treated with PEG-IFN and RBV had their data analyzed. A stepwise logistic regression analysis was performed to identify the variables independently related to SVR. Adverse events were recorded during treatment.Results:308 patients were included, 75% genotype 1 and 23% genotype 3. METAVIR F3 was present in 39% and F4 in 61% of patients. The median Child Pugh score for F4 patients was 5 (5–9). The global SVR rate was 34%, 11% were relapsers and 55% were nonresponders. SVR rates were similar between patients treated with PEG-IFN alfa 2a or alfa 2b (p = 0.24). SVR rates according to Child–Pugh score were 26% (Child A) and 18% (Child B). The independent factors related to SVR in F4 patients were genotype 3, RVR and fewer Child Pugh score points. Treatment interruption occurred in 31% patients and death occurred in 1.9%, all with liver cirrhosis.Conclusion:Treatment of HCV in patients with advanced fibrosis should not be postponed. However, a very careful evaluation of cirrhotic patients must be performed before treatment is indicated and careful monitoring is required during treatment.
publishDate 2014
dc.date.none.fl_str_mv 2014-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702014000100048
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702014000100048
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1016/j.bjid.2013.05.007
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
dc.source.none.fl_str_mv Brazilian Journal of Infectious Diseases v.18 n.1 2014
reponame:Brazilian Journal of Infectious Diseases
instname:Brazilian Society of Infectious Diseases (BSID)
instacron:BSID
instname_str Brazilian Society of Infectious Diseases (BSID)
instacron_str BSID
institution BSID
reponame_str Brazilian Journal of Infectious Diseases
collection Brazilian Journal of Infectious Diseases
repository.name.fl_str_mv Brazilian Journal of Infectious Diseases - Brazilian Society of Infectious Diseases (BSID)
repository.mail.fl_str_mv bjid@bjid.org.br||lgoldani@ufrgs.br
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