Artemisinin Resistance in <i>Plasmodium falciparum</i> Malaria

Arjen M. Dondorp(Mahidol University), François Nosten(Mahidol University), Poravuth Yi(Cambodia National Malaria Center), Debashish Das(Mahidol University), Aung Pyae Phyo(Shoklo Malaria Research Unit), Joel Tärning(Mahidol University), Khin Maung Lwin(Shoklo Malaria Research Unit), Frédéric Ariey(Institut Pasteur du Cambodge), Warunee Hanpithakpong(Mahidol University), Sue J. Lee(Mahidol University), Pascal Ringwald(World Health Organization), Kamolrat Silamut(Mahidol University), Mallika Imwong(Mahidol University), Kesinee Chotivanich(Mahidol University), Pharath Lim(Institut Pasteur du Cambodge), Trent Herdman(Mahidol University), Sen Sam An(Family Health International 360), Shunmay Yeung(Mahidol University), Pratap Singhasivanon(Mahidol University), Nicholas Day(Mahidol University), Niklas Lindegårdh(Mahidol University), Duong Socheat(Cambodia National Malaria Center), Nicholas J. White(Mahidol University)
New England Journal of Medicine
July 29, 2009
Cited by 3,443Open Access
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Abstract

BACKGROUND: Artemisinin-based combination therapies are the recommended first-line treatments of falciparum malaria in all countries with endemic disease. There are recent concerns that the efficacy of such therapies has declined on the Thai-Cambodian border, historically a site of emerging antimalarial-drug resistance. METHODS: In two open-label, randomized trials, we compared the efficacies of two treatments for uncomplicated falciparum malaria in Pailin, western Cambodia, and Wang Pha, northwestern Thailand: oral artesunate given at a dose of 2 mg per kilogram of body weight per day, for 7 days, and artesunate given at a dose of 4 mg per kilogram per day, for 3 days, followed by mefloquine at two doses totaling 25 mg per kilogram. We assessed in vitro and in vivo Plasmodium falciparum susceptibility, artesunate pharmacokinetics, and molecular markers of resistance. RESULTS: We studied 40 patients in each of the two locations. The overall median parasite clearance times were 84 hours (interquartile range, 60 to 96) in Pailin and 48 hours (interquartile range, 36 to 66) in Wang Pha (P<0.001). Recrudescence confirmed by means of polymerase-chain-reaction assay occurred in 6 of 20 patients (30%) receiving artesunate monotherapy and 1 of 20 (5%) receiving artesunate-mefloquine therapy in Pailin, as compared with 2 of 20 (10%) and 1 of 20 (5%), respectively, in Wang Pha (P=0.31). These markedly different parasitologic responses were not explained by differences in age, artesunate or dihydroartemisinin pharmacokinetics, results of isotopic in vitro sensitivity tests, or putative molecular correlates of P. falciparum drug resistance (mutations or amplifications of the gene encoding a multidrug resistance protein [PfMDR1] or mutations in the gene encoding sarco-endoplasmic reticulum calcium ATPase6 [PfSERCA]). Adverse events were mild and did not differ significantly between the two treatment groups. CONCLUSIONS: P. falciparum has reduced in vivo susceptibility to artesunate in western Cambodia as compared with northwestern Thailand. Resistance is characterized by slow parasite clearance in vivo without corresponding reductions on conventional in vitro susceptibility testing. Containment measures are urgently needed. (ClinicalTrials.gov number, NCT00493363, and Current Controlled Trials number, ISRCTN64835265.)


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