Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus

Detalhes bibliográficos
Autor(a) principal: Grando, Aline Vitali
Data de Publicação: 2017
Outros Autores: Ferreira, Paulo Roberto Abrão, Pessôa, Mário Guimarães, Mazo, Daniel Ferraz de Campos, Brandão-Mello, Carlos Eduardo, Reuter, Tânia, Martinelli, Ana de Lourdes Candolo, Gonzalez, Mário Peribanez, Nastri, Ana Catharina Seixas-Santos, Campos, Aléia Faustina, Lopes, Max Igor Banks Ferreira, Brito, José David Urbaez, Mendes-Corrêa, Maria Cássia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista do Instituto de Medicina Tropical de São Paulo
Texto Completo: https://www.revistas.usp.br/rimtsp/article/view/140682
Resumo: Despite recent advances in therapy for chronic hepatitis C (CHC), the disease caused by genotype 3 virus (GEN3) is still considered a treatment challenge in certain patient subgroups. The aim of this retrospective study was to evaluate the effectiveness and safety of the peginterferon (Peg-IFN) and ribavirin (RBV) combination treatment for GEN3/CHC patients, and to evaluate sustained virological response (SVR) indicators and early treatment interruption due to serious adverse events (SAE). This was a retrospective observational study of GEN3/CHC patients, co-infected or not by HIV and treated with Peg-IFN/RBV in nine Brazilian healthcare centers. The study sample included 184 GEN3/CHC patients; 70 (38%) were co-infected with HIV. The overall SVR rate was 57.1% (95% CI 50-64). Among co-infected and mono-infected patients, the SVR rate was 51.4% (36/70) and 60.5% (69/114), respectively (p=0.241). Thirty-four (18.5%) patients experienced SAE and interrupted treatment. SVR was negatively associated with the use of Peg-IFN alpha 2b (PR 0.75; 95% CI 0.58-0.99; p=0.045) and to early treatment interruption due to SAE (PR 0.36; 95% CI 0.20-0.68; p=0.001). Early treatment interruption due to SAE was associated with age (PR 1.06; 95% CI 1.02-1.10; p
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spelling Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virusHepatitis CChronic hepatitis CCoinfection HCV-HIVInterferonsRibavirinHCV genotypes Despite recent advances in therapy for chronic hepatitis C (CHC), the disease caused by genotype 3 virus (GEN3) is still considered a treatment challenge in certain patient subgroups. The aim of this retrospective study was to evaluate the effectiveness and safety of the peginterferon (Peg-IFN) and ribavirin (RBV) combination treatment for GEN3/CHC patients, and to evaluate sustained virological response (SVR) indicators and early treatment interruption due to serious adverse events (SAE). This was a retrospective observational study of GEN3/CHC patients, co-infected or not by HIV and treated with Peg-IFN/RBV in nine Brazilian healthcare centers. The study sample included 184 GEN3/CHC patients; 70 (38%) were co-infected with HIV. The overall SVR rate was 57.1% (95% CI 50-64). Among co-infected and mono-infected patients, the SVR rate was 51.4% (36/70) and 60.5% (69/114), respectively (p=0.241). Thirty-four (18.5%) patients experienced SAE and interrupted treatment. SVR was negatively associated with the use of Peg-IFN alpha 2b (PR 0.75; 95% CI 0.58-0.99; p=0.045) and to early treatment interruption due to SAE (PR 0.36; 95% CI 0.20-0.68; p=0.001). Early treatment interruption due to SAE was associated with age (PR 1.06; 95% CI 1.02-1.10; pUniversidade de São Paulo. Instituto de Medicina Tropical de São Paulo2017-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/xmlhttps://www.revistas.usp.br/rimtsp/article/view/140682Revista do Instituto de Medicina Tropical de São Paulo; Vol. 59 (2017); e67Revista do Instituto de Medicina Tropical de São Paulo; Vol. 59 (2017); e67Revista do Instituto de Medicina Tropical de São Paulo; v. 59 (2017); e671678-99460036-4665reponame:Revista do Instituto de Medicina Tropical de São Pauloinstname:Instituto de Medicina Tropical (IMT)instacron:IMTenghttps://www.revistas.usp.br/rimtsp/article/view/140682/135645https://www.revistas.usp.br/rimtsp/article/view/140682/148453Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Pauloinfo:eu-repo/semantics/openAccessGrando, Aline VitaliFerreira, Paulo Roberto AbrãoPessôa, Mário GuimarãesMazo, Daniel Ferraz de CamposBrandão-Mello, Carlos EduardoReuter, TâniaMartinelli, Ana de Lourdes CandoloGonzalez, Mário PeribanezNastri, Ana Catharina Seixas-SantosCampos, Aléia FaustinaLopes, Max Igor Banks FerreiraBrito, José David UrbaezMendes-Corrêa, Maria Cássia2018-02-23T18:46:02Zoai:revistas.usp.br:article/140682Revistahttp://www.revistas.usp.br/rimtsp/indexPUBhttps://www.revistas.usp.br/rimtsp/oai||revimtsp@usp.br1678-99460036-4665opendoar:2022-12-13T16:52:41.151927Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT)true
dc.title.none.fl_str_mv Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
title Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
spellingShingle Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
Grando, Aline Vitali
Hepatitis C
Chronic hepatitis C
Coinfection HCV-HIV
Interferons
Ribavirin
HCV genotypes
title_short Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
title_full Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
title_fullStr Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
title_full_unstemmed Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
title_sort Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
author Grando, Aline Vitali
author_facet Grando, Aline Vitali
Ferreira, Paulo Roberto Abrão
Pessôa, Mário Guimarães
Mazo, Daniel Ferraz de Campos
Brandão-Mello, Carlos Eduardo
Reuter, Tânia
Martinelli, Ana de Lourdes Candolo
Gonzalez, Mário Peribanez
Nastri, Ana Catharina Seixas-Santos
Campos, Aléia Faustina
Lopes, Max Igor Banks Ferreira
Brito, José David Urbaez
Mendes-Corrêa, Maria Cássia
author_role author
author2 Ferreira, Paulo Roberto Abrão
Pessôa, Mário Guimarães
Mazo, Daniel Ferraz de Campos
Brandão-Mello, Carlos Eduardo
Reuter, Tânia
Martinelli, Ana de Lourdes Candolo
Gonzalez, Mário Peribanez
Nastri, Ana Catharina Seixas-Santos
Campos, Aléia Faustina
Lopes, Max Igor Banks Ferreira
Brito, José David Urbaez
Mendes-Corrêa, Maria Cássia
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Grando, Aline Vitali
Ferreira, Paulo Roberto Abrão
Pessôa, Mário Guimarães
Mazo, Daniel Ferraz de Campos
Brandão-Mello, Carlos Eduardo
Reuter, Tânia
Martinelli, Ana de Lourdes Candolo
Gonzalez, Mário Peribanez
Nastri, Ana Catharina Seixas-Santos
Campos, Aléia Faustina
Lopes, Max Igor Banks Ferreira
Brito, José David Urbaez
Mendes-Corrêa, Maria Cássia
dc.subject.por.fl_str_mv Hepatitis C
Chronic hepatitis C
Coinfection HCV-HIV
Interferons
Ribavirin
HCV genotypes
topic Hepatitis C
Chronic hepatitis C
Coinfection HCV-HIV
Interferons
Ribavirin
HCV genotypes
description Despite recent advances in therapy for chronic hepatitis C (CHC), the disease caused by genotype 3 virus (GEN3) is still considered a treatment challenge in certain patient subgroups. The aim of this retrospective study was to evaluate the effectiveness and safety of the peginterferon (Peg-IFN) and ribavirin (RBV) combination treatment for GEN3/CHC patients, and to evaluate sustained virological response (SVR) indicators and early treatment interruption due to serious adverse events (SAE). This was a retrospective observational study of GEN3/CHC patients, co-infected or not by HIV and treated with Peg-IFN/RBV in nine Brazilian healthcare centers. The study sample included 184 GEN3/CHC patients; 70 (38%) were co-infected with HIV. The overall SVR rate was 57.1% (95% CI 50-64). Among co-infected and mono-infected patients, the SVR rate was 51.4% (36/70) and 60.5% (69/114), respectively (p=0.241). Thirty-four (18.5%) patients experienced SAE and interrupted treatment. SVR was negatively associated with the use of Peg-IFN alpha 2b (PR 0.75; 95% CI 0.58-0.99; p=0.045) and to early treatment interruption due to SAE (PR 0.36; 95% CI 0.20-0.68; p=0.001). Early treatment interruption due to SAE was associated with age (PR 1.06; 95% CI 1.02-1.10; p
publishDate 2017
dc.date.none.fl_str_mv 2017-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/rimtsp/article/view/140682
url https://www.revistas.usp.br/rimtsp/article/view/140682
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/rimtsp/article/view/140682/135645
https://www.revistas.usp.br/rimtsp/article/view/140682/148453
dc.rights.driver.fl_str_mv Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Paulo
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Revista do Instituto de Medicina Tropical de São Paulo
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
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dc.publisher.none.fl_str_mv Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo
publisher.none.fl_str_mv Universidade de São Paulo. Instituto de Medicina Tropical de São Paulo
dc.source.none.fl_str_mv Revista do Instituto de Medicina Tropical de São Paulo; Vol. 59 (2017); e67
Revista do Instituto de Medicina Tropical de São Paulo; Vol. 59 (2017); e67
Revista do Instituto de Medicina Tropical de São Paulo; v. 59 (2017); e67
1678-9946
0036-4665
reponame:Revista do Instituto de Medicina Tropical de São Paulo
instname:Instituto de Medicina Tropical (IMT)
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instname_str Instituto de Medicina Tropical (IMT)
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reponame_str Revista do Instituto de Medicina Tropical de São Paulo
collection Revista do Instituto de Medicina Tropical de São Paulo
repository.name.fl_str_mv Revista do Instituto de Medicina Tropical de São Paulo - Instituto de Medicina Tropical (IMT)
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