Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/134077
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Type: Journal article
Title: Paritaprevir, ritonavir, ombitasvir, and dasabuvir with and without ribavirin in people with HCV genotype 1 and recent injecting drug use or receiving opioid substitution therapy
Author: Grebely, J.
Conway, B.
Cunningham, E.B.
Fraser, C.
Moriggia, A.
Gane, E.
Stedman, C.
Cooper, C.
Castro, E.
Schmid, P.
Petoumenos, K.
Hajarizadeh, B.
Marks, P.
Erratt, A.
Dalgard, O.
Lacombe, K.
Feld, J.J.
Bruneau, J.
Daulouede, J.P.
Powis, J.
et al.
Citation: International Journal of Drug Policy, 2018; 62:94-103
Publisher: Elsevier
Issue Date: 2018
ISSN: 0955-3959
1873-4758
Statement of
Responsibility: 
Jason Grebelya, Brian Conwayb, Evan B. Cunninghama, Chris Fraserc, Alberto Moriggiad, Ed Ganee, Catherine Stedmanf, Curtis Cooperg, Erika Castroh, Patrick Schmidi, Kathy Petoumenosa, Behzad Hajarizadeha, Phillipa Marksa, Amanda Erratta, Olav Dalgardj, Karine Lacombek, Jordan J. Feldl, Julie Bruneaum, Jean-Pierre Dauloueden, Jeff Powiso, Philip Bruggmannp, Gail V. Matthewsa, Ian Kronborgq, David Shawr, Adrian Dunlops, Margaret Hellardt, Tanya L. Applegatea, Sione Crawfordu, Gregory J Dorea, on behalf of the D3FEAT Study Group
Abstract: Background: Direct-acting antiviral therapy for hepatitis C virus (HCV) infection is safe and effective, but there are little data among people who have recently injected drugs. This study evaluated the efficacy, and safety of paritaprevir/ritonavir, ombitasvir, dasabuvir with or without ribavirin for chronic HCV genotype (G) 1 among people with recent injecting drug use and/or receiving OST. Methods: D3FEAT is an international open-label study that recruited treatment-naïve participants with recent injecting drug use (previous 6 months) and/or receiving OST with chronic HCV G1 infection between June 2016 and February 2017 in seven countries. Participants received paritaprevir/ritonavir, ombitasvir, dasabuvir with (G1a) or without ribavirin (G1b) administered twice daily in a one-week electronic blister pack (records timing of each dose) for 12 weeks. The primary endpoint was undetectable HCV RNA 12 weeks post-treatment (SVR12). Results: Among 87 participants (median age 48 years), 23% were female, 8% had cirrhosis, and 90% had G1a. Overall, 71% were receiving OST, 61% injected in the previous six months, 45% injected in the previous month, and 15% injected > daily. Treatment completion was 97% (84 of 87). There were no virological breakthroughs, but three discontinuations (loss to follow-up, n = 1; non-adherence, n = 1; incarceration, n = 1). SVR was 91% (79 of 87, 95% CI, 83%–96%). Five participants who completed treatment did not have SVR (loss to follow-up, n = 1; death, n = 1; virologic relapse, n = 3). Drug use prior to and during treatment did not impact SVR12. Treatment-related adverse events were observed in 46 (53%) patients (six grade 3, no grade 4). Five (6%) patients had at least one serious adverse event (two possibly/probably related to therapy; nausea and myoclonus). Two cases of reinfection were observed. Conclusion: Paritaprevir/ritonavir, ombitasvir, and dasabuvir with or without ribavirin for 12 weeks is effective among people with HCV genotype 1 with recent injecting drug use and/or receiving OST.
Keywords: Hepatitis C; Treatment; PWID; Drug use; Injecting drug users; DAA
Rights: © 2018 Elsevier B.V. All rights reserved.
DOI: 10.1016/j.drugpo.2018.10.004
Grant ID: NHMRC
Published version: http://dx.doi.org/10.1016/j.drugpo.2018.10.004
Appears in Collections:Medicine publications

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