Ribavirin at the Era of Novel Direct Antiviral Agents for the Treatment of Hepatitis C Virus Infection: Relevance of Pharmacological Monitoring

Author:

Pradat Pierre123ORCID,Virlogeux Victor14ORCID,Gagnieu Marie-Claude5,Zoulim Fabien1236,Bailly François123

Affiliation:

1. Department of Hepatology, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, 103 grande rue de la Croix-Rousse, 69004 Lyon, France

2. INSERM U1052, 69003 Lyon, France

3. Université Lyon I, Lyon, France

4. Ecole Normale Supérieure, 69007 Lyon, France

5. Department of Pharmacology, Hôpital Edouard Herriot, Hospices Civils de Lyon, 69003 Lyon, France

6. Institut Universitaire de France, Paris, France

Abstract

Ribavirin is often used for the treatment of hepatitis C virus (HCV) infection. Although its mechanisms of action remain to be clearly elucidated, ribavirin plays a beneficial role for achieving virological response and decreasing the rate of virological relapse after treatment cessation. However, ribavirin may induce side effects leading to early treatment discontinuation. Among them, hemolytic anemia is the most frequent and results from intraerythrocyte accumulation. Pharmacological studies have shown that early ribavirin exposure assessed by the area under the curve (AUC) at day 0 and ribavirin trough concentration during the first three months of therapy were correlated with sustained virological response (SVR). These studies highlighted the relevance of ribavirin pharmacologic monitoring and early dose adaptation during therapy. Although the role of ribavirin within new direct acting antiviral (DAA) combinations will probably decrease in the future, its potential benefit in difficult-to-treat patients such as patients with severe hepatopathy or patients who failed triple therapy including patients with multiresistance will need to be further investigated.

Publisher

Hindawi Limited

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