Hepatitis C late relapse in patients with directly acting antiviral-related sustained virological response at week 12.
Adult
Aged
Aged, 80 and over
Antiviral Agents
/ therapeutic use
Drug Resistance, Viral
Drug Therapy, Combination
Female
Genotype
Hepacivirus
/ drug effects
Hepatitis C, Chronic
/ drug therapy
Humans
Interferons
/ therapeutic use
Male
Middle Aged
Recurrence
Sequence Analysis, DNA
Sustained Virologic Response
Time Factors
Treatment Failure
Viral Nonstructural Proteins
/ genetics
DAA
HCV infection
non-response
relapse
Journal
Liver international : official journal of the International Association for the Study of the Liver
ISSN: 1478-3231
Titre abrégé: Liver Int
Pays: United States
ID NLM: 101160857
Informations de publication
Date de publication:
05 2019
05 2019
Historique:
received:
31
08
2018
revised:
21
11
2018
accepted:
02
12
2018
pubmed:
17
12
2018
medline:
22
9
2020
entrez:
17
12
2018
Statut:
ppublish
Résumé
The aim of the present study was to identify, among the patients with failure to DAA regimen, those with a late relapse (after the achievement of a sustained virological response at week 12) and to characterize the clinical, epidemiological and virological features of these patients. A total of 129 HCV patients with non-response to an IFN-free regimen were enrolled. Sanger sequencing of NS3, NS5A and NS5B was performed at failure by home-made protocols. Of the 129 patients enrolled, 8 (6.2%) experienced a breakthrough, 15 (11.7%) non-response, 99 (76.7%) a relapse by week 12 after the end of DAA therapy, and 7 (5.4%) a late relapse (after week 12; median 24 weeks, range 24-72). For two of the seven patients with a late relapse, a serum sample collected before the start of the DAA regimen was available; phylogenetic analysis showed no change in sequences of NS3, NS5A and NS5B regions, suggesting a reactivation of the initial HCV strain; for the remaining five patients, no serum collected before the DAA regimen was available, and thus, a re-infection cannot be excluded. Although a late relapse is infrequent, the study suggests a post-treatment follow-up of 72 weeks.
Substances chimiques
Antiviral Agents
0
NS3 protein, hepatitis C virus
0
Viral Nonstructural Proteins
0
Interferons
9008-11-1
NS-5 protein, hepatitis C virus
EC 2.7.7.48
Banques de données
GENBANK
['NC_004102', 'D90208']
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
844-853Informations de copyright
© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.