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Effectiveness of interferon-free therapy for the treatment of HCV-patients with compensated cirrhosis treated through the Irish early access program.

Authors :
Gray E
O'Leary A
Bergin C
Cannon M
Courtney G
Crosbie O
De Gascun CF
Fanning LJ
Feeney E
Houlihan DD
Kelleher B
Lambert JS
Lee J
Mallon P
McConkey S
McCormick A
McKiernan S
McNally C
Murray F
Sheehan G
Stewart S
Walsh C
Norris S
Source :
Expert review of gastroenterology & hepatology [Expert Rev Gastroenterol Hepatol] 2017 Jun; Vol. 11 (6), pp. 593-601. Date of Electronic Publication: 2017 Feb 22.
Publication Year :
2017

Abstract

Background: We investigated the real-world effectiveness of interferon-free regimens for the treatment of patients with compensated cirrhosis infected with hepatitis C virus (HCV).<br />Method: Using the Irish national HCV treatment registry, the effectiveness and safety of interferon-free regimens for HCV-infected patients treated between April 2015 and August 2016, was determined.<br />Results: A SVR12 was achieved in 86% of subjects treated with sofosbuvir/ledipasvir ± ribavirin (SOF/LDV±RBV), 93% treated with paritaprevir, ombitasvir and ritonavir combined with dasabuvir ± ribavirin (3D±RBV) and 89% treated with sofosbuvir/daclatasvir ± ribavirin (SOF/DCV±RBV). The discontinuation rate was 5% and the on-treatment mortality rate was 1%.<br />Conclusion: The availability of interferon-free regimens represents a significant breakthrough for the treatment of HCV infection. Treatments options, with high SVR12 rates, are now available for patients with compensated cirrhosis who were unsuitable for treatment with interferon-based regimens. Data obtained from studies conducted in real world practice provide robust information fundamental for input into future economic evaluations for agents used for the treatment of HCV infection.

Details

Language :
English
ISSN :
1747-4132
Volume :
11
Issue :
6
Database :
MEDLINE
Journal :
Expert review of gastroenterology & hepatology
Publication Type :
Academic Journal
Accession number :
28276815
Full Text :
https://doi.org/10.1080/17474124.2017.1292850