Ombitasvir/paritaprevir/ritonavir and dasabuvir±ribavirin for chronic HCV infection in US veterans with psychiatric disorders.

HCV GT1 SVR comorbidity direct-acting antiviral substance-related disorders veterans

Journal

Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 15 05 2019
accepted: 09 12 2019
medline: 13 12 2019
pubmed: 13 12 2019
entrez: 13 12 2019
Statut: ppublish

Résumé

Hepatitis C virus (HCV) infections are more common among US veterans receiving care through Veterans Affairs (VA) Medical Centers than among the general population. Historically, HCV therapies had lower efficacy rates in VA patients, possibly due to common comorbidities such as psychiatric disorders and substance abuse. The direct-acting antivirals ombitasvir/paritaprevir/ritonavir and dasabuvir (OBV/PTV/r+DSV)±ribavirin (RBV) are approved in the US for HCV genotype 1 (GT1)-infected adults with or without cirrhosis. This study prospectively evaluated the safety and efficacy of OBV/PTV/r+DSV±RBV in VA patients with HCV GT1 infection. TOPAZ-VA was a phase 3b, open-label trial. Adult US veterans with HCV GT1 infection, without cirrhosis or with compensated cirrhosis, were eligible for enrollment. Patients with GT1a infection received OBV/PTV/r +DSV+RBV for 12 weeks or 24 weeks (for those with cirrhosis); GT1b-infected patients without cirrhosis received OBV/PTV/r +DSV for 12 weeks; those with cirrhosis received OBV/PTV/r +DSV with RBV. The primary endpoint was sustained virologic response at posttreatment week 12 (SVR12); safety was also assessed. Ninety-nine patients were enrolled at 10 sites from May through November 2015. The majority were male (96%), white (60%), and with GT1a infection (68%); 49% reported ongoing psychiatric disorders. Overall, 94% (93/99) achieved SVR12; three patients had a virologic failure. The most common AEs were fatigue (28%), headache (20%), and nausea (15%); six patients discontinued treatment due to AEs. In US veterans with HCV GT1 infection, OBV/PTV/r +DSV±RBV yielded a 94% overall SVR12 rate and was well tolerated. The presence of psychiatric disorders and/or injection drug use did not impact efficacy.

Identifiants

pubmed: 31829433
doi: 10.1002/jmv.25655
pmc: PMC7687116
mid: NIHMS1647884
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3459-3464

Subventions

Organisme : CSRD VA
ID : I01 CX000295
Pays : United States
Organisme : Intramural VA
ID : VA999999
Pays : United States
Organisme : AbbVie

Informations de copyright

© 2019 The Authors. Journal of Medical Virology Published by Wiley Periodicals, Inc.

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Auteurs

Michael Fuchs (M)

Hepatology Section, Hunter Holmes McGuire VA Medical Center, Virginia Commonwealth University, Richmond, Virginia.

Alexander Monto (A)

Department of Gastroenterology, San Francisco VA Medical Center, San Francisco, California.

Norbert Bräu (N)

Viral Hepatitis Program, James J Peters VA Medical Center, New York City, New York.

Mariem Charafeddine (M)

AbbVie Inc, North Chicago, Illinois.

Warren Schmidt (W)

Department of Internal Medicine, Iowa City VA Healthcare System, Iowa City, Iowa.

Michael Kozal (M)

Department of Internal Medicine, VA Connecticut Healthcare System, Yale School of Medicine, Yale University, New Haven, Connecticut.

Susanna Naggie (S)

Department of Medicine, Durham VA Medical Center, Durham, North Carolina.

Ramsey Cheung (R)

Department of Gastroenterology and Hepatology, VA Palo Alto Healthcare System, Palo Alto, California.

Gretja Schnell (G)

AbbVie Inc, North Chicago, Illinois.

Yao Yu (Y)

AbbVie Inc, North Chicago, Illinois.

Kristine Richards (K)

AbbVie Inc, North Chicago, Illinois.

Victoria Mullally (V)

AbbVie Inc, North Chicago, Illinois.

Daniel E Cohen (DE)

AbbVie Inc, North Chicago, Illinois.

Doris Toro (D)

Gastroenterology Section, VA Caribbean Healthcare System, San Juan, Puerto Rico.

Classifications MeSH