Rare HCV subtypes and retreatment outcomes in a cohort of European DAA-experienced patients
0301 basic medicine
Hepatitis C Virus
0303 health sciences
treatment response
610
rare HCV genotypes
resistance-associated substitutions
RC799-869
Diseases of the digestive system. Gastroenterology
Direct-acting antivirals
Research Article
DOI:
10.1016/j.jhepr.2024.101072
Publication Date:
2024-03-25T17:50:15Z
AUTHORS (320)
ABSTRACT
BackgroundData on the prevalence and characteristics of so called rare HCV genotypes (GT) in larger cohorts is limited. This study investigates frequency GT resistance-associated substitutions efficacy retreatment a European cohort.MethodsA total 129 patients with GT1-6 were included from resistance database. NS3, NS5A NS5B sequenced clinical parameters efficacies collected retrospectively.ResultsOverall 1.5% (69/4656) DAA-naïve 4.4% (60/1376) DAA-failure infected GT. While almost equally distributed throughout patients, we detected mainly GT4 (47%, 28/60 GT4; these n=17, subtype 4r) GT3 (25%, 15/60 GT3, n=8, 3b) among DAA-failures. 62% (37/60) DAA failures had not responded to first-generation regimes majority was (57%, 21/37). In contrast, failure pangenotypic regimens (38%, 23/60), infections overrepresented 13/23). RASs uncommon GT2, GT5a GT6, observed combined GT1, at positions 28, 30, 31, which can be considered as inherent. completed follow-up retreatment, achieved high SVR rate (94%, 45/48 mITT; 92%, 45/49 ITT). Three GT4f, 4r or 3b, respectively, virological treatment failure.ConclusionsIn this cohort, uncommon. Accumulation specific suggests reduced antiviral activities regimens. The limited global availability for first line therapy well multiple targeted could result elimination targets being delayed.Impact implicationsData are still scarce. found low rates HCV-infected patients. subtypes accumulated after 1st generation viral 30 31. delayed.
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