Plasmodium falciparum clearance in clinical studies of artesunate-amodiaquine and comparator treatments in sub-Saharan Africa, 1999-2009

被引:23
作者
Zwang, Julien [1 ]
Dorsey, Grant [2 ]
Martensson, Andreas [3 ]
d'Alessandro, Umberto [4 ]
Ndiaye, Jean-Louis [5 ]
Karema, Corine [6 ]
Djimde, Abdoulaye [7 ]
Brasseur, Philippe [8 ]
Sirima, Sodiomon B. [9 ]
Olliaro, Piero [10 ,11 ]
机构
[1] Drugs Neglected Dis Initiat DNDi, Geneva, Switzerland
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[3] Karolinska Inst, Dept Publ Hlth Sci, Div Global Hlth IHCAR, Stockholm, Sweden
[4] MRC Unit, Banjul, Gambia
[5] Cheikh Anta Diop Univ, Fac Med, Dept Parasitol, Dakar, Senegal
[6] Minist Hlth, Malaria & Other Parasit Dis Div RBC, Rugenge, Kigali, Rwanda
[7] Univ Sci Tech & Technol Bamako, Fac Med & Pharm, Dept Epidemiol Parasit Dis, Malaria Res & Training Ctr, Bamako, Mali
[8] Inst Rech Dev, Unite Mixte Rech 198, Dakar, Senegal
[9] Minist Sante, Ctr Natl Rech & Format Paludisme, Ouagadougou, Burkina Faso
[10] UNICEF UNDP WB WHO Special Programme Res & Traini, Geneva, Switzerland
[11] Univ Oxford, Churchill Hosp, Nuffield Dept Med, Ctr Trop Med & Vaccinol, Oxford OX3 7LJ, England
关键词
ARTEMISININ COMBINATION THERAPIES; PLUS SULFADOXINE-PYRIMETHAMINE; FIXED-DOSE COMBINATIONS; UNCOMPLICATED MALARIA; PARASITE CLEARANCE; ARTEMETHER-LUMEFANTRINE; MOLECULAR MARKERS; NIMBA COUNTY; OPEN-LABEL; IN-VIVO;
D O I
10.1186/1475-2875-13-114
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Artemisinin-based combination therapy (ACT) is the recommended first-line therapy for uncomplicated Plasmodium falciparum malaria worldwide but decreased artemisinin susceptibility, phenotypically characterized as slow parasite clearance time (PCT), has now been reported in Southeast Asia. This makes it all too important to measure the dynamics of parasite clearance in African patients treated with ACT over time, to understand trends and detect changes early enough to intervene Methods: Individual patient data from 27 clinical trials of artesunate-amodiaquine (ASAQ) vs comparators conducted between 1999 and 2009 were analysed for parasite clearance on modified intent-to-treat (ITT) basis. Results: Overall 15,017 patients treated for uncomplicated P. falciparum malaria at 44 sites in 20 sub-Saharan African countries were included in the analysis; 51% (n=7,660) vs 49% (n=7,357) were treated with ASAQ and comparator treatments, respectively. Seventy-seven per cent (77%) were children under six years of age. The proportion of the patients treated with ASAQ with persistent parasitaemia on Day 2 was 8.6%, and 1.5% on Day 3. Risk factor for not clearing parasites on Day 2 and Day 3 calculated by multivariate logistic regression with random effect on site and controlling for treatment were: high parasitaemia before treatment was (adjusted risk ratios (AOR) 2.12, 95% CI 1.91-2.35, AOR 2.43, 95% CI 1.98-3.00, respectively); non-ACT treatment (p=0.001, for all comparisons). Anaemia (p=0.001) was an additional factor for Day 2 and young age (p=0.005) for Day 3. In patients treated with ASAQ in studies who had complete parasitaemia data every 24 hours up to Day 3 and additionally Day 7, the parasite reduction ratio was 93.9% by Day 1 and 99.9% by Day 2. Using the median parasitaemia before treatment (p0=27,125 mu L) and a fitted model, the predicted PCT (pPCT =3.614*ln (p0) - 6.135, r(2) = 0.94) in ASAQ recipients was 31 hours. Conclusion: Within the period covered by these studies, rapid Plasmodium falciparum clearance continues to be achieved in Sub-Saharan African patients treated with ACT, and in particular with ASAQ. The prediction formula for parasite clearance time could be a pragmatic tool for studies with binary outcomes and once-daily sampling, both for research and monitoring purposes.
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