Prevalence of resistance-associated substitutions to NS3, NS5A and NS5B inhibitors at DAA-failure in hepatitis C virus in Italy from 2015 to 2019.


Journal

Le infezioni in medicina
ISSN: 2532-8689
Titre abrégé: Infez Med
Pays: Italy
ID NLM: 9613961

Informations de publication

Date de publication:
01 Jun 2021
Historique:
entrez: 1 6 2021
pubmed: 2 6 2021
medline: 31 8 2021
Statut: ppublish

Résumé

Despite the high efficacy of direct-acting antivirals (DAAs), the selection of resistance-associated substitutions (RASs) after virological failure of hepatitis C virus (HCV) DAAs can impair the cure of chronic HCV. The aim of the study was to characterize RASs after virological failure of DAAs in Italy over the years. Within the Italian network VIRONET-C, the change in prevalence of NS3/4A-NS5A-NS5B RASs was retrospectively evaluated in patients who failed a DAA regimen over the years 2015-2019. NS3, NS5A and NS5B Sanger sequencing was performed using homemade protocols and the geno2pheno system was used to define HCV-genotype/subtype and predict drug resistance. The changes in the prevalence of RASs over time were evaluated using the chi-square test for trend. Predictors of RASs at failure were analysed by logistic regression. Among 468 HCV-infected patients, HCV genotype 1 was the most prevalent (1b in 154, 33% and 1a in 109, 23%). DAA regimens were: ledipasvir (LDV)/sofosbuvir (SOF) in 131 patients (28%), daclatasvir (DCV)/SOF in 109 (23%), ombitasvir/paritaprevir/ritonavir+dasabuvir (3D) in 89 (19%), elbasvir (EBR)/grazoprevir (GRZ) in 52 (10.5%), velpatasvir (VEL)/SOF in 53 (11%), glecaprevir (GLE)/pibrentasvir (PIB) in 27 (6%) and ombitasvir/paritaprevir/ritonavir (2D) in 7 (1.5%); ribavirin was administered in 133 (28%). The NS5A fasta sequence was available for all patients, NS5B and NS3/4A both for 93%. The prevalence of NS5A and NS3/4A RASs significantly declined from 2015 to 2019; NS5B RAS remained stable. Independent predictors of any RASs included older age and genotype 1a (vs G2 and vs G4). Notably, at least partial susceptibility to all the agents included in the GLE/PIB and VEL/SOF/Voxilaprevir (VOX) combinations was predicted in >95% of cases. As RASs remain common at the failure of DAAs, their identification could play a crucial role in optimizing re-treatment strategies. In Italy RAS prevalence has been decreasing over the years and susceptibility to the latest developed drug combinations is maintained in most cases.

Identifiants

pubmed: 34061790

Substances chimiques

Antiviral Agents 0
Benzimidazoles 0
Carbamates 0
Drug Combinations 0
Fluorenes 0
Heterocyclic Compounds, 4 or More Rings 0
Macrocyclic Compounds 0
Sulfonamides 0
ledipasvir, sofosbuvir drug combination 0
sofosbuvir velpatasvir voxilaprevir drug combination 0
Ribavirin 49717AWG6K
velpatasvir KCU0C7RS7Z
Sofosbuvir WJ6CA3ZU8B

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

242-251

Auteurs

Barbara Rossetti (B)

Department of Specialized and Internal Medicine, Tropical and Infectious Diseases Unit, University Hospital of Siena, Siena, Italy.

Lorenzo Paglicci (L)

Department of Specialized and Internal Medicine, Tropical and Infectious Diseases Unit, University Hospital of Siena, Siena, Italy; Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Velia C Di Maio (VC)

Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy.

Chiara Cassol (C)

Department of Specialized and Internal Medicine, Tropical and Infectious Diseases Unit, University Hospital of Siena, Siena, Italy; Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Silvia Barbaliscia (S)

Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy.

Stefania Paolucci (S)

Molecular Virology Unit, Microbiology and Virology Department, IRCCS Polyclinic Foundation San Matteo, Pavia, Italy.

Bianca Bruzzone (B)

Hygiene Unit, IRCCS AOU San Martino-IST, Genoa, Italy.

Nicola Coppola (N)

Department of Mental Health and Public Medicine, Infectious Diseases Unit, University of Campania "L. Vanvitelli", Naples, Italy.

Francesca Montagnani (F)

Department of Specialized and Internal Medicine, Tropical and Infectious Diseases Unit, University Hospital of Siena, Siena, Italy; Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Valeria Micheli (V)

Clinical Microbiology, Virology and Bioemergencies, ASST Fatebenefratelli Sacco University Hospital, Milan, Italy.

Laura Monno (L)

Infectious Diseases Unit, University of Bari, Bari, Italy.

Giacomo Zanelli (G)

Department of Specialized and Internal Medicine, Tropical and Infectious Diseases Unit, University Hospital of Siena, Siena, Italy; Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Teresa Santantonio (T)

Infectious Diseases Unit, University of Foggia, Foggia, Italy.

Nunzia Cuomo (N)

Microbiology and Virology Unit, Azienda Ospedaliera Specialistica dei Colli Monaldi - Cotugno - C.T.O., Naples, Italy.

Cinzia Caudai (C)

Microbiology and Virology Unit, AOU Senese, Siena, Italy.

Maurizio Zazzi (M)

Department of Medical Biotechnologies, University of Siena, Siena, Italy.

Francesca Ceccherini-Silberstein (F)

Department of Experimental Medicine, University of Rome Tor Vergata, Rome, Italy.

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Classifications MeSH