Modelling the impact of deferring HCV treatment on liver-related complications in HIV coinfected men who have sex with men
Authored by Cindy Zahnd, Luisa Salazar-Vizcaya, Jean-Francois Dufour, Beat Mullhaupt, Gilles Wandeler, Roger Kouyos, Janne Estill, Barbara Bertisch, Andri Rauch, Olivia Keiser, HIV Swiss, Hepatitis C Cohort Studies Swiss
Date Published: 2016
DOI: 10.1016/j.jhep.2016.02.030
Sponsors:
Swiss National Science Foundation (SNSF)
Cancer Research Switzerland
Platforms:
R
Model Documentation:
Other Narrative
Model Code URLs:
Model code not found
Abstract
Background \& Aims: Hepatitis C (HCV) is a leading cause of morbidity
and mortality in people who live with HIV. In many countries, access to
direct acting antiviral agents to treat HCV is restricted to individuals
with advanced liver disease (METAVIR stage F3 or F4). Our goal was to
estimate the long term impact of deferring HCV treatment for men who
have sex with men (MSM) who are coinfected with HIV and often have
multiple risk factors for liver disease progression.
Methods: We developed an individual-based model of liver disease
progression in HIV/HCV coinfected MSM. We estimated liver-related
morbidity and mortality as well as the median time spent with
replicating HCV infection when individuals were treated in liver
fibrosis stages F0, F1, F2, F3 or F4 on the METAVIR scale.
Results: The percentage of individuals who died of liver-related
complications was 2\% if treatment was initiated in F0 or F1. It
increased to 3\% if treatment was deferred until F2, 7\% if it was
deferred until F3 and 22\% if deferred until F4. The median time
individuals spent with replicating HCV increased from 5 years if
treatment was initiated in F2 to almost 15 years if it was deferred
until F4.
Conclusions: Deferring HCV therapy until advanced liver fibrosis is
established could increase liver-related morbidity and mortality in
HIV/HCV coinfected individuals, and substantially prolong the time
individuals spend with a replicating HCV infection. (C) 2016 European
Association for the Study of the Liver. Published by Elsevier B.V. All
rights reserved.
Tags
cost-effectiveness
Therapy
Hepatitis-c virus
Cohort
Genotype 1
Direct-acting antivirals
Sustained virological
response
Interferon plus ribavirin
Infected
patients
Fibrosis progression