Reinfection Following Successful Direct-acting Antiviral Therapy for Hepatitis C Virus Infection Among People Who Inject Drugs.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
26 04 2021
Historique:
received: 20 11 2019
accepted: 10 03 2020
pubmed: 14 3 2020
medline: 21 5 2021
entrez: 14 3 2020
Statut: ppublish

Résumé

The aim of this analysis was to calculate the incidence of hepatitis C virus (HCV) reinfection and associated factors among 2 clinical trials of HCV direct-acting antiviral treatment in people with recent injecting drug use or currently receiving opioid agonist therapy (OAT). Participants who achieved an end-of-treatment response in 2 clinical trials of people with recent injecting drug use or currently receiving OAT (SIMPLIFY and D3FEAT) enrolled between March 2016 and February 2017 in 8 countries were assessed for HCV reinfection, confirmed by viral sequencing. Incidence was calculated using person-time of observation and associated factors were assessed using Cox proportional hazard models. Seventy-three percent of the population at risk of reinfection (n = 177; median age, 48 years; 73% male) reported ongoing injecting drug use. Total follow-up time at risk was 254 person-years (median, 1.8 years; range, 0.2-2.8 years). Eight cases of reinfection were confirmed for an incidence of 3.1/100 person-years (95% confidence interval [CI], 1.6-6.3) overall and 17.9/100 person-years (95% CI, 5.8-55.6) among those who reported sharing needles/syringes. Younger age and needle/syringe sharing were associated with HCV reinfection. These data demonstrate the need for ongoing monitoring and improved strategies to prevent HCV reinfection following successful treatment among people with ongoing injecting drug use to achieve HCV elimination. NCT02336139 and NCT02498015.

Sections du résumé

BACKGROUND
The aim of this analysis was to calculate the incidence of hepatitis C virus (HCV) reinfection and associated factors among 2 clinical trials of HCV direct-acting antiviral treatment in people with recent injecting drug use or currently receiving opioid agonist therapy (OAT).
METHODS
Participants who achieved an end-of-treatment response in 2 clinical trials of people with recent injecting drug use or currently receiving OAT (SIMPLIFY and D3FEAT) enrolled between March 2016 and February 2017 in 8 countries were assessed for HCV reinfection, confirmed by viral sequencing. Incidence was calculated using person-time of observation and associated factors were assessed using Cox proportional hazard models.
RESULTS
Seventy-three percent of the population at risk of reinfection (n = 177; median age, 48 years; 73% male) reported ongoing injecting drug use. Total follow-up time at risk was 254 person-years (median, 1.8 years; range, 0.2-2.8 years). Eight cases of reinfection were confirmed for an incidence of 3.1/100 person-years (95% confidence interval [CI], 1.6-6.3) overall and 17.9/100 person-years (95% CI, 5.8-55.6) among those who reported sharing needles/syringes. Younger age and needle/syringe sharing were associated with HCV reinfection.
CONCLUSIONS
These data demonstrate the need for ongoing monitoring and improved strategies to prevent HCV reinfection following successful treatment among people with ongoing injecting drug use to achieve HCV elimination.
CLINICAL TRIALS REGISTRATION
NCT02336139 and NCT02498015.

Identifiants

pubmed: 32166305
pii: 5804220
doi: 10.1093/cid/ciaa253
doi:

Substances chimiques

Antiviral Agents 0
Pharmaceutical Preparations 0

Banques de données

ClinicalTrials.gov
['NCT02336139', 'NCT02498015']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1392-1400

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Evan B Cunningham (EB)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.

Behzad Hajarizadeh (B)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.

Janaki Amin (J)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.
Faculty of Medicine and Health Sciences, Macquarie University, Sydney, Australia.

Margaret Hellard (M)

The Burnet Institute, Melbourne, Australia.
Department of Infectious Disease, The Alfred Hospital, Melbourne, Australia.

Julie Bruneau (J)

Centre Hospitalier de l'Université de Montréal, Montreal, Canada.

Jordan J Feld (JJ)

Toronto General Hospital, Toronto, Canada.

Curtis Cooper (C)

Ottawa Hospital Research Institute, Ottawa, Canada.

Jeff Powis (J)

South Riverdale Community Health Centre, Toronto, Canada.

Alain H Litwin (AH)

Albert Einstein College of Medicine, New York, New York, USA.

Philippa Marks (P)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.

Olav Dalgard (O)

Akershus University Hospital, Oslo, Norway.

Brian Conway (B)

Vancouver Infectious Diseases Center, Vancouver, Canada.

Alberto Moriggia (A)

Fondazione Epatocentro Ticino, Lugano, Switzerland.
Ingrado Addiction Services, Lugano, Switzerland.

Catherine Stedman (C)

Christchurch Hospital and University of Otago, Christchurch, New Zealand.

Phillip Read (P)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.
Kirketon Road Centre, Sydney, Australia.

Philip Bruggmann (P)

Arud Centres for Addiction Medicine, Zurich, Switzerland.

Karine Lacombe (K)

Inserm UMR-S1136, Sorbonne Université, Hôpital Saint-Antoine, Paris, France.

Adrian Dunlop (A)

Newcastle Pharmacotherapy Service, Newcastle, Australia.

Tanya L Applegate (TL)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.

Gail V Matthews (GV)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.
St Vincent's Hospital, Sydney, Australia.

Chris Fraser (C)

Coolaid Community Health Centre, Victoria, Canada.

Gregory J Dore (GJ)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.
St Vincent's Hospital, Sydney, Australia.

Jason Grebely (J)

The Kirby Institute, University of New South Wales Sydney, Sydney, Australia.

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Classifications MeSH