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First-wave protease inhibitors for hepatitis C genotype 1 treatment: a real-life experience in Brazilian patients
Chachá, Silvana Gama Florencio; Rodrigues, João Paulo Vilela; Araújo, Roberta Chaves; Pereira, Leonardo Régis Leira; Villanova, Márcia Guimarães; Souza, Fernanda Fernandes; Santana, Rodrigo de Carvalho; Martinelli, Ana de Lourdes Candolo.
Afiliación
  • Chachá, Silvana Gama Florencio; Universidade Federal de São Carlos. Departamento de Medicina. São Carlos. BR
  • Rodrigues, João Paulo Vilela; Universidade Federal de São Carlos. Departamento de Medicina. São Carlos. BR
  • Araújo, Roberta Chaves; Universidade Federal de São Carlos. Departamento de Medicina. São Carlos. BR
  • Pereira, Leonardo Régis Leira; Universidade Federal de São Carlos. Departamento de Medicina. São Carlos. BR
  • Villanova, Márcia Guimarães; Universidade Federal de São Carlos. Departamento de Medicina. São Carlos. BR
  • Souza, Fernanda Fernandes; Universidade Federal de São Carlos. Departamento de Medicina. São Carlos. BR
  • Santana, Rodrigo de Carvalho; Universidade Federal de São Carlos. Departamento de Medicina. São Carlos. BR
  • Martinelli, Ana de Lourdes Candolo; Universidade Federal de São Carlos. Departamento de Medicina. São Carlos. BR
Rev. Soc. Bras. Med. Trop ; 51(2): 146-154, Mar.-Apr. 2018. tab, graf
Article en En | LILACS | ID: biblio-897067
Biblioteca responsable: BR1.1
ABSTRACT
Abstract

INTRODUCTION:

Licensed for chronic hepatitis C treatment in 2011, the protease inhibitors (PIs) telaprevir (TVR) and boceprevir (BOC), which have high sustained viral responses (SVR), ushered a new era characterized by the development of direct-action drugs against the hepatitis C virus (HCV). The aim of this study was to analyze the effectiveness and safety of BOC and TVR administered with pegylated interferon and ribavirin and to share the experience of a Brazilian reference center.

METHODS:

A retrospective descriptive study was conducted in patients with HCV genotype 1 infection who started treatment between July 2013 and December 2015. Data were collected using a computerized system.

RESULTS:

A total of 115 subjects were included, of which 58 (50.4 %) had liver cirrhosis and 103 (89.6 %) used TVR. The overall SVR rate was 61.7 % (62.1 % for TVR and 58.3 % for BOC). The presence of cirrhosis was associated with a lower SVR rate, whereas patients who relapsed after prior therapy had a greater chance of showing SVR than did non-responders. The incidence of adverse drug reactions (ADRs) was high. Almost all patients (~100 %) presented with hematologic events. Furthermore, treatment had to be discontinued in 15 subjects (13 %) due to severe ADRs.

CONCLUSIONS:

In conclusion, the SVR rates in our study were lower than those reported in pre-marketing studies but were comparable to real-life data. ADRs, particularly hematological ADRs, were more common compared to those in previous studies and resulted in a high rate of treatment discontinuity.
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Texto completo: 1 Colección: 01-internacional Base de datos: LILACS Asunto principal: Antivirales / Inhibidores de Proteasas / Hepacivirus / Hepatitis C Crónica Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male País/Región como asunto: America do sul / Brasil Idioma: En Revista: Rev. Soc. Bras. Med. Trop Asunto de la revista: MEDICINA TROPICAL Año: 2018 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Brasil

Texto completo: 1 Colección: 01-internacional Base de datos: LILACS Asunto principal: Antivirales / Inhibidores de Proteasas / Hepacivirus / Hepatitis C Crónica Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Male País/Región como asunto: America do sul / Brasil Idioma: En Revista: Rev. Soc. Bras. Med. Trop Asunto de la revista: MEDICINA TROPICAL Año: 2018 Tipo del documento: Article País de afiliación: Brasil Pais de publicación: Brasil