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Int J Drug Policy. 2017 Sep;47:177-186. doi: 10.1016/j.drugpo.2017.05.020. Epub 2017 Jun 16.

Efficacy of response-guided directly observed pegylated interferon and self-administered ribavirin for people who inject drugs with hepatitis C virus genotype 2/3 infection: The ACTIVATE study.

Author information

1
The Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia. Electronic address: jgrebely@kirby.unsw.edu.au.
2
Akershus University Hospital, Oslo, Norway; University of Oslo, Oslo, Norway.
3
The Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia.
4
The Liver Unit, Queen Mary University of London, London, United Kingdom.
5
Arud Centres for Addiction Medicine, Zurich, Switzerland.
6
Vancouver Infectious Diseases Center, Vancouver, British Columbia, Canada.
7
Ludwig Maximilians-University Munich, Munich, Germany.
8
Department of Gastroenterology and Hepatology, Ziekenhuis Oost Limburg, Genk, Belgium; Department of Hepatology, UZ Leuven, Leuven, Belgium; Faculty of Medicine and Life Sciences, Hasselt University, Hasselt, Belgium.
9
International Network on Hepatitis in Substance Users, New York, NY, United States.
10
The Kirby Institute, UNSW Sydney, Sydney, New South Wales, Australia; Faculty of Medicine and Health Sciences, Macquarie University, Sydney, Australia.
11
Nepean Hospital, Sydney, New South Wales, Australia.
12
Royal Adelaide Hospital, Adelaide, South Australia, Australia.
13
School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia.
14
Burnet Institute, Melbourne, Victoria, Australia.
15
Research Center, Centre Hospitalier de l'Universite de Montreal (CRCHUM), Montreal, Quebec, Canada.
16
Department of Infectious Diseases, Akershus University Hospital, Norway; Institute for Clinical Medicine, University of Oslo, Norway; Department of Gastroenterology, Oslo University Hospital, Norway.
17
Stuivenberg ZNA, Antwerp, Belgium.
18
Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.

Abstract

BACKGROUND:

There are few data on treatment for hepatitis C virus (HCV) infection among people with ongoing injecting drug use. This study evaluated the efficacy of response-guided therapy for chronic HCV genotypes 2/3 infection among people with ongoing injecting drug use or receiving opioid substitution therapy (OST). A secondary aim was to identify predictors of HCV treatment response.

METHODS:

ACTIVATE was a multicentre clinical trial recruited between 2012 and 2014. Participants with genotypes 2/3 were treated with directly observed peg-interferon alfa-2b and self-administered ribavirin for 12 (undetectable HCV RNA at week 4) or 24 weeks (detectable HCV RNA at week 4). Participants were recruited from drug treatment clinics, private practices, hospital clinics and community clinics in Australia, Canada, and five countries in Europe. The primary study outcome was sustained virological response (SVR, undetectable HCV RNA >12 weeks post-treatment).

RESULTS:

Among 93 people with ongoing injecting drug use or receiving OST treated for HCV genotype 2/3, 59% had recently (past month) injected drugs, 77% were receiving OST and 56% injected drugs during therapy. Overall SVR was 66% (61/93). SVR was 84% in those with undetectable HCV RNA at week 4 (12 weeks) compared to 38% in those without (24 weeks). In adjusted analysis, cirrhosis vs. no/mild fibrosis [adjusted OR (aOR) 0.33, 95% CI 0.13, 0.86] predicted reduced SVR, while response at week 4 was associated with increased SVR [aOR 8.11, 95% CI 2.73, 24.10]. Recent injecting drug use at baseline or during therapy was not associated with SVR.

CONCLUSION:

This study demonstrates that people with recent injecting drug use or OST with chronic HCV can achieve responses to interferon-based therapy similar to other populations, despite injecting drugs prior to or during therapy. Cirrhosis was predictive of reduced response to HCV therapy, while response at week 4 (despite shortened therapy) was predictive of improved response.

KEYWORDS:

Drug use; HCV treatment; Hepatitis C; PWID

PMID:
28624134
DOI:
10.1016/j.drugpo.2017.05.020
[Indexed for MEDLINE]

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