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Effectiveness and Safety of Pangenotypic Regimens in the Most Difficult to Treat Population of Genotype 3 HCV Infected Cirrhotics

There is still limited data available from real-world experience studies on the pangenotypic regimens in patients with genotype (GT) 3 hepatitis C virus (HCV) infection and liver cirrhosis. The current study aimed to evaluate the efficacy and safety of pangenotypic regimens in this difficult-to-trea...

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Detalles Bibliográficos
Autores principales: Zarębska-Michaluk, Dorota, Jaroszewicz, Jerzy, Parfieniuk-Kowerda, Anna, Janczewska, Ewa, Dybowska, Dorota, Pawłowska, Małgorzata, Halota, Waldemar, Mazur, Włodzimierz, Lorenc, Beata, Janocha-Litwin, Justyna, Simon, Krzysztof, Piekarska, Anna, Berak, Hanna, Klapaczyński, Jakub, Stępień, Piotr, Sobala-Szczygieł, Barbara, Citko, Jolanta, Socha, Łukasz, Tudrujek-Zdunek, Magdalena, Tomasiewicz, Krzysztof, Sitko, Marek, Dobracka, Beata, Krygier, Rafał, Białkowska-Warzecha, Jolanta, Laurans, Łukasz, Flisiak, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8347334/
https://www.ncbi.nlm.nih.gov/pubmed/34362064
http://dx.doi.org/10.3390/jcm10153280
Descripción
Sumario:There is still limited data available from real-world experience studies on the pangenotypic regimens in patients with genotype (GT) 3 hepatitis C virus (HCV) infection and liver cirrhosis. The current study aimed to evaluate the efficacy and safety of pangenotypic regimens in this difficult-to-treat population. A total of 236 patients with mean age 52.3 ± 11.3 years and male predominance (72%) selected from EpiTer-2 database were included in the analysis; 72% of them were treatment-naïve. The majority of patients (55%) received the combination of sofosbuvir/velpatasvir (SOF/VEL), 71 without and 58 with ribavirin (RBV), whereas the remaining 107 individuals were assigned to glecaprevir/pibrentasvir (GLE/PIB). The effectiveness of the treatment following GLE/PIB and SOF/VEL regimens (96% and 93%) was higher compared to SOF/VEL + RBV option (79%). The univariate analysis demonstrated the significantly lower sustained virologic response in males, in patients with baseline HCV RNA ≥ 1,000,000 IU/mL, and among those who failed previous DAA-based therapy. The multivariate logistic regression analysis recognized only the male gender and presence of ascites at baseline as the independent factors of non-response to treatment. It should be emphasized that despite the availability of pangenotypic, strong therapeutic options, GT3 infected patients with cirrhosis still remain difficult-to-treat, especially those with hepatic impairment and DAA-experienced.