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

Authors :
Dorota Zarębska-Michaluk
Jerzy Jaroszewicz
Anna Parfieniuk-Kowerda
Ewa Janczewska
Dorota Dybowska
Małgorzata Pawłowska
Waldemar Halota
Włodzimierz Mazur
Beata Lorenc
Justyna Janocha-Litwin
Krzysztof Simon
Anna Piekarska
Hanna Berak
Jakub Klapaczyński
Piotr Stępień
Barbara Sobala-Szczygieł
Jolanta Citko
Łukasz Socha
Magdalena Tudrujek-Zdunek
Krzysztof Tomasiewicz
Marek Sitko
Beata Dobracka
Rafał Krygier
Jolanta Białkowska-Warzecha
Łukasz Laurans
Robert Flisiak
Source :
Journal of Clinical Medicine, Vol 10, Iss 15, p 3280 (2021)
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

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.

Details

Language :
English
ISSN :
20770383
Volume :
10
Issue :
15
Database :
Directory of Open Access Journals
Journal :
Journal of Clinical Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.95b8d74b90cf4019ac8ed54f0598a2e8
Document Type :
article
Full Text :
https://doi.org/10.3390/jcm10153280