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

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...

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Veröffentlicht in:Revista do Instituto de Medicina Tropical de São Paulo 2017-11, Vol.59, p.e67-8
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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
ISSN:0036-4665
1678-9946
1678-9946
0036-4665
DOI:10.1590/S1678-9946201759067