Show simple item record

dc.contributor.authorRobaeys, Gen_US
dc.contributor.authorChristensen, Sen_US
dc.contributor.authorLucidarme, Den_US
dc.contributor.authorArain, Aen_US
dc.contributor.authorBruggmann, Pen_US
dc.contributor.authorKunkel, Jen_US
dc.contributor.authorKeim, Sen_US
dc.contributor.authorJäkel, Men_US
dc.contributor.authorDeMasi, Ren_US
dc.contributor.authorLiu, Cen_US
dc.contributor.authorLonjon-Domanec, Ien_US
dc.contributor.authorFoster, GRen_US
dc.date.accessioned2017-08-07T14:31:46Z
dc.date.issued2017-06en_US
dc.date.submitted2017-06-26T09:39:50.877Z
dc.identifier.issn2193-8229en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/25097
dc.description.abstractINTRODUCTION: People who inject drugs represent an under-treated chronic hepatitis C virus (HCV)-infected patient population. METHODS: INTEGRATE was a prospective, observational study investigating the effectiveness, safety, and adherence in routine clinical practice to telaprevir in combination with peg-interferon and ribavirin (Peg-IFN/RBV) in patients with history of injecting drug use chronically infected with genotype 1 HCV. RESULTS: A total of 46 patients were enrolled and included in the intent-to-treat (ITT) population. Among heroin and/or cocaine users (n = 37; 80%), 22% reported use in the past month; 74% (34/46) of patients were on opioid substitution therapy in the pre-treatment phase, and 43% (20/46) discontinued HCV treatment prematurely. Sustained virologic response rate was 54% (25/46) in the ITT population and 74% (25/34) in the per protocol (evaluable-for-effectiveness) population. The main reason for failure in the ITT analysis was loss to follow-up (n = 8; 17%). Adverse events occurred in 91% (42/46) of patients. Mean patient-reported adherence to study drugs was >89% at Week 4, Week 12 and end of treatment. CONCLUSION: Despite a high rate of treatment discontinuation (including loss to follow-up), self-reported adherence to treatment was good and virologic cure rates were similar to those reported in large real-world cohorts. Our findings suggest that people with a history of injecting drug use should be considered for treatment of chronic HCV infection, and highlight the need for improvements in patient support to boost retention in care and, in turn, help to prevent reinfection and transmission. CLINICAL TRIAL REGISTRATION: Clinicaltrials.gov identifier, NCT01980290. FUNDING: Janssen Pharmaceuticals.en_US
dc.format.extent265 - 275en_US
dc.languageengen_US
dc.relation.ispartofInfect Dis Theren_US
dc.rightsThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/ by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
dc.subjectHCVen_US
dc.subjectInjection drug usersen_US
dc.subjectOpioid substitution therapyen_US
dc.subjectPWIDen_US
dc.subjectRetention in careen_US
dc.subjectTelapreviren_US
dc.titleChronic Hepatitis C Treatment in Patients with Drug Injection History: Findings of the INTEGRATE Prospective, Observational Study.en_US
dc.typeArticle
dc.rights.holder© The Author(s) 2017.
dc.identifier.doi10.1007/s40121-017-0158-xen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/28477061en_US
pubs.issue2en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume6en_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record