An individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment
Copyright © 2020 Francis et al. Treating malaria in HIV-coinfected individuals should consider potential drug-drug interactions. Artemether-lumefantrine is the most widely recommended treatment for uncomplicated malaria globally. Lumefantrine is metabolized by CYP3A4, an enzyme that commonly used an...
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th-mahidol.545992020-05-05T13:03:01Z An individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment Jose Francis Karen I. Barnes Lesley Workman Tamara Kredo Lasse S. Vestergaard Richard M. Hoglund Pauline Byakika-Kibwika Mohammed Lamorde Stephen I. Walimbwa Ifeyinwa Chijioke-Nwauche Colin J. Sutherland Concepta Merry Kimberley K. Scarsi Nyagonde Nyagonde Martha M. Lemnge Saye H. Khoo Ib C. Bygbjerg Sunil Parikh Francesca T. Aweeka Joel Tarning Paolo Denti Makerere University National Institute For Medical Research Tanzania London School of Hygiene & Tropical Medicine Københavns Universitet University of Port Harcourt South African Medical Research Council Statens Serum Institut University of California, San Francisco University of Liverpool University of Nebraska Medical Center Mahidol University Trinity College Dublin Nuffield Department of Clinical Medicine Yale University University of Cape Town 4Muheza District Hospital Asia Regional Centre Medicine Pharmacology, Toxicology and Pharmaceutics Copyright © 2020 Francis et al. Treating malaria in HIV-coinfected individuals should consider potential drug-drug interactions. Artemether-lumefantrine is the most widely recommended treatment for uncomplicated malaria globally. Lumefantrine is metabolized by CYP3A4, an enzyme that commonly used antiretrovirals often induce or inhibit. A population pharmacokinetic meta-analysis was conducted using individual participant data from 10 studies with 6,100 lumefantrine concentrations from 793 nonpregnant adult participants (41% HIV-malaria-coinfected, 36% malaria-infected, 20% HIV-infected, and 3% healthy volunteers). Lumefantrine exposure increased 3.4-fold with coadministration of lopinavirritonavir- based antiretroviral therapy (ART), while it decreased by 47% with efavirenzbased ART and by 59% in the patients with rifampin-based antituberculosis treatment. Nevirapine- or dolutegravir-based ART and malaria or HIV infection were not associated with significant effects. Monte Carlo simulations showed that those on concomitant efavirenz or rifampin have 49% and 80% probability of day 7 concentrations <200 ng/ml, respectively, a threshold associated with an increased risk of treatment failure. The risk of achieving subtherapeutic concentrations increases with larger body weight. An extended 5-day and 6-day artemether-lumefantrine regimen is predicted to overcome these drug-drug interactions with efavirenz and rifampin, respectively. 2020-05-05T05:34:46Z 2020-05-05T05:34:46Z 2020-05-01 Article Antimicrobial Agents and Chemotherapy. Vol.64, No.5 (2020) 10.1128/AAC.02394-19 10986596 00664804 2-s2.0-85083651265 https://repository.li.mahidol.ac.th/handle/123456789/54599 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85083651265&origin=inward |
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Medicine Pharmacology, Toxicology and Pharmaceutics Jose Francis Karen I. Barnes Lesley Workman Tamara Kredo Lasse S. Vestergaard Richard M. Hoglund Pauline Byakika-Kibwika Mohammed Lamorde Stephen I. Walimbwa Ifeyinwa Chijioke-Nwauche Colin J. Sutherland Concepta Merry Kimberley K. Scarsi Nyagonde Nyagonde Martha M. Lemnge Saye H. Khoo Ib C. Bygbjerg Sunil Parikh Francesca T. Aweeka Joel Tarning Paolo Denti An individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment |
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Copyright © 2020 Francis et al. Treating malaria in HIV-coinfected individuals should consider potential drug-drug interactions. Artemether-lumefantrine is the most widely recommended treatment for uncomplicated malaria globally. Lumefantrine is metabolized by CYP3A4, an enzyme that commonly used antiretrovirals often induce or inhibit. A population pharmacokinetic meta-analysis was conducted using individual participant data from 10 studies with 6,100 lumefantrine concentrations from 793 nonpregnant adult participants (41% HIV-malaria-coinfected, 36% malaria-infected, 20% HIV-infected, and 3% healthy volunteers). Lumefantrine exposure increased 3.4-fold with coadministration of lopinavirritonavir- based antiretroviral therapy (ART), while it decreased by 47% with efavirenzbased ART and by 59% in the patients with rifampin-based antituberculosis treatment. Nevirapine- or dolutegravir-based ART and malaria or HIV infection were not associated with significant effects. Monte Carlo simulations showed that those on concomitant efavirenz or rifampin have 49% and 80% probability of day 7 concentrations <200 ng/ml, respectively, a threshold associated with an increased risk of treatment failure. The risk of achieving subtherapeutic concentrations increases with larger body weight. An extended 5-day and 6-day artemether-lumefantrine regimen is predicted to overcome these drug-drug interactions with efavirenz and rifampin, respectively. |
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Makerere University |
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Makerere University Jose Francis Karen I. Barnes Lesley Workman Tamara Kredo Lasse S. Vestergaard Richard M. Hoglund Pauline Byakika-Kibwika Mohammed Lamorde Stephen I. Walimbwa Ifeyinwa Chijioke-Nwauche Colin J. Sutherland Concepta Merry Kimberley K. Scarsi Nyagonde Nyagonde Martha M. Lemnge Saye H. Khoo Ib C. Bygbjerg Sunil Parikh Francesca T. Aweeka Joel Tarning Paolo Denti |
format |
Article |
author |
Jose Francis Karen I. Barnes Lesley Workman Tamara Kredo Lasse S. Vestergaard Richard M. Hoglund Pauline Byakika-Kibwika Mohammed Lamorde Stephen I. Walimbwa Ifeyinwa Chijioke-Nwauche Colin J. Sutherland Concepta Merry Kimberley K. Scarsi Nyagonde Nyagonde Martha M. Lemnge Saye H. Khoo Ib C. Bygbjerg Sunil Parikh Francesca T. Aweeka Joel Tarning Paolo Denti |
author_sort |
Jose Francis |
title |
An individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment |
title_short |
An individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment |
title_full |
An individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment |
title_fullStr |
An individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment |
title_full_unstemmed |
An individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment |
title_sort |
individual participant data population pharmacokinetic meta-analysis of drug-drug interactions between lumefantrine and commonly used antiretroviral treatment |
publishDate |
2020 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/54599 |
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1763489948437053440 |