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

Authors :
Zarębska-Michaluk D
Jaroszewicz J
Parfieniuk-Kowerda A
Janczewska E
Dybowska D
Pawłowska M
Halota W
Mazur W
Lorenc B
Janocha-Litwin J
Simon K
Piekarska A
Berak H
Klapaczyński J
Stępień P
Sobala-Szczygieł B
Citko J
Socha Ł
Tudrujek-Zdunek M
Tomasiewicz K
Sitko M
Dobracka B
Krygier R
Białkowska-Warzecha J
Laurans Ł
Flisiak R
Source :
Journal of clinical medicine [J Clin Med] 2021 Jul 25; Vol. 10 (15). Date of Electronic Publication: 2021 Jul 25.
Publication Year :
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 :
2077-0383
Volume :
10
Issue :
15
Database :
MEDLINE
Journal :
Journal of clinical medicine
Publication Type :
Academic Journal
Accession number :
34362064
Full Text :
https://doi.org/10.3390/jcm10153280