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A cost-effectiveness analysis of shortened direct-acting antiviral treatment in genotype 1 noncirrhotic treatment-naive patients with chronic Hepatitis C virus
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1-s2.0-S1098301519301019-main.pdf | Published version | 1.12 MB | Adobe PDF | View/Open |
Title: | A cost-effectiveness analysis of shortened direct-acting antiviral treatment in genotype 1 noncirrhotic treatment-naive patients with chronic Hepatitis C virus |
Authors: | Fawsitt, CG Vickerman, P Cooke, G Welton, NJ STOP-HCV Consortium |
Item Type: | Journal Article |
Abstract: | BACKGROUND: Direct-acting antivirals are successful in curing hepatitis C virus infection in more than 95% of patients treated for 12 weeks, but they are expensive. Shortened treatment durations, which may have lower cure rates, have been proposed to reduce costs. OBJECTIVES: To evaluate the lifetime cost-effectiveness of different shortened treatment durations for genotype 1 noncirrhotic treatment-naive patients. METHODS: Assuming a UK National Health Service perspective, we used a probabilistic decision tree and Markov model to compare 3 unstratified shortened treatment durations (8, 6, and 4 weeks) against a standard 12-week treatment duration. Patients failing shortened first-line treatment were re-treated with a 12-week treatment regimen. Parameter inputs were taken from published studies. RESULTS: The 8-week treatment duration had an expected incremental net monetary benefit of £7737 (95% confidence interval £3242-£11 819) versus the standard 12-week treatment, per 1000 patients. The 6-week treatment had a positive incremental net monetary benefit, although some uncertainty was observed. The probability that the 8- and 6-week treatments were the most cost-effective was 56% and 25%, respectively, whereas that for the 4-week treatment was 17%. Results were generally robust to sensitivity analyses, including a threshold analysis that showed that the 8-week treatment was the most cost-effective at all drug prices lower than £40 000 per 12-week course. CONCLUSIONS: Shortening treatments licensed for 12 weeks to 8 weeks is cost-effective in genotype 1 noncirrhotic treatment-naive patients. There was considerable uncertainty in the estimates for 6- and 4-week treatments, with some indication that the 6-week treatment may be cost-effective. |
Issue Date: | 1-Jun-2019 |
Date of Acceptance: | 29-Dec-2018 |
URI: | http://hdl.handle.net/10044/1/70572 |
DOI: | https://dx.doi.org/10.1016/j.jval.2018.12.011 |
ISSN: | 1098-3015 |
Publisher: | Elsevier |
Start Page: | 693 |
End Page: | 703 |
Journal / Book Title: | Value in Health |
Volume: | 22 |
Issue: | 6 |
Copyright Statement: | © 2019 ISPOR-The Professional Society for Health Economics and Outcomes Research. Published by Elsevier Inc. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
Sponsor/Funder: | National Institute for Health Research Medical Research Council (MRC) National Institute for Health Research |
Funder's Grant Number: | EME/14/02/17 MR/P025064/1 RP-2016-07-012 |
Keywords: | cost-effectiveness direct-acting antivirals hepatitis C virus shortened treatment duration STOP-HCV Consortium cost-effectiveness direct-acting antivirals hepatitis C virus shortened treatment duration 1117 Public Health and Health Services 1402 Applied Economics Health Policy & Services |
Publication Status: | Published |
Conference Place: | United States |
Online Publication Date: | 2019-05-17 |
Appears in Collections: | Department of Medicine (up to 2019) |