Is hepatitis C direct-acting antiviral therapy a risk factor for the development and recurrence of hepatocellular carcinoma? Narrative literature review and clinical practice recommendations

Loading...
Thumbnail Image
Identifiers

Publication date

Authors

Delgado Martínez, Carolina
Gómez Rubio, Mariano
Gómez Domínguez, Cecilia

Advisors

Editors

Journal Title

Journal ISSN

Volume Title

Publisher

Metrics

Google Scholar

Research Projects

Organizational Units

Journal Issue

Abstract

The development of direct-acting antivirals (DAAs) has been a turning point in chronic hepatitis C treatment. With an efficacy rate on viral eradication close to 100% and an excellent safety profile, they have replaced interferon-based treatments as first-line therapy for hepatitis C virus (HCV). Following the encouraging results observed during the first years with these treatments, new publications suggested an unexpectedly high incidence of hepatocellular carcinoma (HCC) in patients previously treated with DAAs as well as a higher HCC recurrence rate in them. The possible interaction between DAAs and HCC and its impact on HCC incidence and recurrence still remains controversial. The aim of the present work is to review the current state of the matter by analyzing studies that evaluate the association between chronic hepatitis C treatment with DAAs and the development of HCC either de novo or as a recurrence. Following this, clinical practice recommendations are done.

Description

UNESCO Subjects

Keywords

Bibliographic reference

Delgado-Martínez, C., Gómez-Rubio, M., & Gómez-Domínguez, C. (2021). Is hepatitis C direct-acting antiviral therapy a risk factor for the development and recurrence of hepatocellular carcinoma? Narrative literature review and clinical practice recommendations. Annals of Hepatology, 21, 100225. https://doi.org/10.1016/j.aohep.2020.05.007

Type of document

Attribution-NonCommercial-NoDerivatives 4.0 Internacional

La licencia de este ítem se describe como Attribution-NonCommercial-NoDerivatives 4.0 Internacional