Drug-Drug Interactions Potential of Direct-Acting Antivirals for the treatment of Chronic Hepatitis C Virus infection

被引:17
作者
Neant, Nadege [1 ]
Solas, Caroline [1 ]
机构
[1] Aix Marseille Univ, Hop La Timone, APHM,Lab Pharmacocinet & Toxicol, SMARTc,CRCM,Inserm,UMR1068,CNRS,UMR7258, Marseille, France
关键词
Hepatitis C virus; Direct-acting antiviral; Pharmacokinetics; Drug-drug interactions; MILK THISTLE; SOFOSBUVIR; HCV; HIV; PHARMACOKINETICS; DACLATASVIR; PHARMACODYNAMICS; AMIODARONE; LEDIPASVIR; AGENTS;
D O I
10.1016/j.ijantimicag.2018.10.014
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The advent of direct-acting antiviral agents (DAAs) has transformed the hepatitis C virus (HCV) therapeutic landscape in terms of efficacy and safety, with a cure rate of more than 90%. However, an important potential for drug-drug interactions (DDIs) is expected with these combinations, particularly in patients with other comorbidities (e.g. HIV co-infection, cardiovascular diseases). Each DAA can be a substrate, an inhibitor and/or an inducer of metabolic enzymes and drug efflux transporters. DAAs can act as both victims and perpetrators of DDIs and can sometimes increase the risk and/or intensity of side effects or limit the efficacy of treatment. Therefore, knowledge and management of DDIs with DAAs should be considered a key issue of HCV therapy. This review describes the pharmacokinetic profile of currently used and recommended DAA regimens and summarizes available data regarding DDIs to optimize HCV treatment in clinical practice. (c) 2018 Published by Elsevier B.V.
引用
收藏
页数:7
相关论文
共 47 条
[1]  
[Anonymous], SUMM PROD CHAR EPCL
[2]  
[Anonymous], 2018, EASL RECOMMENDATIONS
[3]  
[Anonymous], REC TEST MAN TREAT H
[4]   Interaction Between Amiodarone and Sofosbuvir-based Treatment for Hepatitis C Virus Infection: Potential Mechanisms and Lessons to be Learned [J].
Back, David J. ;
Burger, David M. .
GASTROENTEROLOGY, 2015, 149 (06) :1315-1317
[5]   Assessment of pharmacokinetic interactions of the HCV NS5A replication complex inhibitor daclatasvir with antiretroviral agents: ritonavir-boosted atazanavir, efavirenz and tenofovir [J].
Bifano, Marc ;
Hwang, Carey ;
Oosterhuis, Berend ;
Hartstra, Jan ;
Grasela, Dennis ;
Tiessen, Renger ;
Velinova-Donga, Maria ;
Kandoussi, Hamza ;
Sevinsky, Heather ;
Bertz, Richard .
ANTIVIRAL THERAPY, 2013, 18 (07) :931-940
[6]   Increasing use of 'party drugs' in people living with HIV on antiretrovirals: a concern for patient safety [J].
Bracchi, Margherita ;
Stuart, David ;
Castles, Richard ;
Khoo, Saye ;
Back, David ;
Boffito, Marta .
AIDS, 2015, 29 (13) :1585-1592
[7]   Pharmacokinetic drug evaluation of velpatasvir plus sofosbuvir for the treatment of hepatitis C virus infection [J].
Brieva, Teresa ;
Rivero, Antonio ;
Rivero-Juarez, Antonio .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2017, 13 (04) :483-490
[8]   Clinical management of drug-drug interactions in HCV therapy: Challenges and solutions [J].
Burger, David ;
Back, David ;
Buggisch, Peter ;
Buti, Maria ;
Craxi, Antonio ;
Foster, Graham ;
Klinker, Hartwig ;
Larrey, Dominique ;
Nikitin, Igor ;
Pol, Stanislas ;
Puoti, Massimo ;
Romero-Gomez, Manuel ;
Wedemeyer, Heiner ;
Zeuzem, Stefan .
JOURNAL OF HEPATOLOGY, 2013, 58 (04) :792-800
[9]   Cardiac Harms of Sofosbuvir: Systematic Review and Meta-Analysis [J].
Caldeira, Daniel ;
Rodrigues, Filipe B. ;
Duarte, Marta M. ;
Sterrantino, Carmelo ;
Barra, Marcio ;
Goncalves, Nilza ;
Pinto, Fausto J. ;
Ferreira, Joaquim J. ;
Costa, Joao .
DRUG SAFETY, 2018, 41 (01) :77-86
[10]  
Caro L, 2017, ANTIMICROB AGENTS CH, V61, DOI [10.1128/aac.00813-17, 10.1128/AAC.00813-17]