Peginterferon still has a place in the treatment of hepatitis C caused by genotype 3 virus
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , , , |
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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Revista do Instituto de Medicina Tropical de São Paulo |
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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 application/xml |
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) instacron:IMT |
instname_str |
Instituto de Medicina Tropical (IMT) |
instacron_str |
IMT |
institution |
IMT |
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) |
repository.mail.fl_str_mv |
||revimtsp@usp.br |
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