Systematic review of artesunate pharmacokinetics: Implication for treatment of resistant malaria
Background: Artesunate (ART) is an artemisinin derivative used as monotherapy for the treatment of severe malaria and in combination with a partner drug for non-severe malaria. Resistance of malaria parasites to artemisinins have emerged in Southeast Asia. Adjustment of drug regimen may be an option...
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doaj-bffc9dab954b4c7ea88d94ac66dcac552020-11-24T21:11:16ZengElsevierInternational Journal of Infectious Diseases1201-97122019-12-01893044Systematic review of artesunate pharmacokinetics: Implication for treatment of resistant malariaYobouet Ines Kouakou0Michel Tod1Gilles Leboucher2Adeline Lavoignat3Guillaume Bonnot4Anne-Lise Bienvenu5Stephane Picot6ICBMS CNRS 5246, SMITh, Malaria Research Unit, Campus Lyon-Tech La Doua, Lyon University, Lyon, FranceGroupement Hospitalier Nord, Service Pharmacie, Hospices Civils de Lyon, Lyon, FranceGroupement Hospitalier Nord, Service Pharmacie, Hospices Civils de Lyon, Lyon, FranceICBMS CNRS 5246, SMITh, Malaria Research Unit, Campus Lyon-Tech La Doua, Lyon University, Lyon, FranceICBMS CNRS 5246, SMITh, Malaria Research Unit, Campus Lyon-Tech La Doua, Lyon University, Lyon, FranceICBMS CNRS 5246, SMITh, Malaria Research Unit, Campus Lyon-Tech La Doua, Lyon University, Lyon, France; Groupement Hospitalier Nord, Service Pharmacie, Hospices Civils de Lyon, Lyon, France; Corresponding author at: Groupement Hospitalier Nord, Service Pharmacie, Hospices Civils de Lyon, 103 Grande Rue de la Croix-Rousse, F-69004, Lyon, France.ICBMS CNRS 5246, SMITh, Malaria Research Unit, Campus Lyon-Tech La Doua, Lyon University, Lyon, France; Groupement Hospitalier Nord, Institut de Parasitologie et Mycologie Médicale, Hospices Civils de Lyon, Lyon, FranceBackground: Artesunate (ART) is an artemisinin derivative used as monotherapy for the treatment of severe malaria and in combination with a partner drug for non-severe malaria. Resistance of malaria parasites to artemisinins have emerged in Southeast Asia. Adjustment of drug regimen may be an option to prevent therapeutic failures considering the relative favourable safety profile of ART high doses. Methods: For that purpose, a systematic review was done using PubMed, Scopus and Web of Science databases. All studies on ART and DHA pharmacokinetic post-administration of artesunate in human patients or volunteers were included. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) checklist 2009 was used. Findings: Fifty studies exploring oral, intravenous, rectal, and intramuscular route (1470 persons, volunteers and patients) were included. Correlations between artesunate doses and Cmax or AUC0-∞ of dihydroartemisinin (DHA) and DHA + ART were evaluated. This correlation was good (R2 > 0.9) using intravenous (IV) route. DHA and ART + DHA average concentrations (Cav) were well above estimated in vivo half-maximal effective concentration (EC50) for intravenous route, but this was not the case for oral route. Interpretation: The favorable Cav/EC50 ratio for IV route provides evidence that IV ART will remain efficient even in the case of increased resistance level, whereas for the oral route, a two-fold increase in EC50 may lead to therapeutic failures, thus providing a rationale for oral dose escalation. Considering the inter-individual variability of ART pharmacokinetic, Therapeutic Drug Monitoring through antimalarial stewardship activities is needed to optimize drug exposure and avoid resistance development. Keywords: Artesunate, Dihydroartemisinin, Pharmacokinetic, Systematic review, Correlation analysis, Inter-individual variability, Dose escalation, Average concentration over timehttp://www.sciencedirect.com/science/article/pii/S120197121930356X |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yobouet Ines Kouakou Michel Tod Gilles Leboucher Adeline Lavoignat Guillaume Bonnot Anne-Lise Bienvenu Stephane Picot |
spellingShingle |
Yobouet Ines Kouakou Michel Tod Gilles Leboucher Adeline Lavoignat Guillaume Bonnot Anne-Lise Bienvenu Stephane Picot Systematic review of artesunate pharmacokinetics: Implication for treatment of resistant malaria International Journal of Infectious Diseases |
author_facet |
Yobouet Ines Kouakou Michel Tod Gilles Leboucher Adeline Lavoignat Guillaume Bonnot Anne-Lise Bienvenu Stephane Picot |
author_sort |
Yobouet Ines Kouakou |
title |
Systematic review of artesunate pharmacokinetics: Implication for treatment of resistant malaria |
title_short |
Systematic review of artesunate pharmacokinetics: Implication for treatment of resistant malaria |
title_full |
Systematic review of artesunate pharmacokinetics: Implication for treatment of resistant malaria |
title_fullStr |
Systematic review of artesunate pharmacokinetics: Implication for treatment of resistant malaria |
title_full_unstemmed |
Systematic review of artesunate pharmacokinetics: Implication for treatment of resistant malaria |
title_sort |
systematic review of artesunate pharmacokinetics: implication for treatment of resistant malaria |
publisher |
Elsevier |
series |
International Journal of Infectious Diseases |
issn |
1201-9712 |
publishDate |
2019-12-01 |
description |
Background: Artesunate (ART) is an artemisinin derivative used as monotherapy for the treatment of severe malaria and in combination with a partner drug for non-severe malaria. Resistance of malaria parasites to artemisinins have emerged in Southeast Asia. Adjustment of drug regimen may be an option to prevent therapeutic failures considering the relative favourable safety profile of ART high doses. Methods: For that purpose, a systematic review was done using PubMed, Scopus and Web of Science databases. All studies on ART and DHA pharmacokinetic post-administration of artesunate in human patients or volunteers were included. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) checklist 2009 was used. Findings: Fifty studies exploring oral, intravenous, rectal, and intramuscular route (1470 persons, volunteers and patients) were included. Correlations between artesunate doses and Cmax or AUC0-∞ of dihydroartemisinin (DHA) and DHA + ART were evaluated. This correlation was good (R2 > 0.9) using intravenous (IV) route. DHA and ART + DHA average concentrations (Cav) were well above estimated in vivo half-maximal effective concentration (EC50) for intravenous route, but this was not the case for oral route. Interpretation: The favorable Cav/EC50 ratio for IV route provides evidence that IV ART will remain efficient even in the case of increased resistance level, whereas for the oral route, a two-fold increase in EC50 may lead to therapeutic failures, thus providing a rationale for oral dose escalation. Considering the inter-individual variability of ART pharmacokinetic, Therapeutic Drug Monitoring through antimalarial stewardship activities is needed to optimize drug exposure and avoid resistance development. Keywords: Artesunate, Dihydroartemisinin, Pharmacokinetic, Systematic review, Correlation analysis, Inter-individual variability, Dose escalation, Average concentration over time |
url |
http://www.sciencedirect.com/science/article/pii/S120197121930356X |
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