Primaquine to reduce transmission of Plasmodium falciparum malaria in Mali : a single-blind, dose-ranging, adaptive randomised phase 2 trial
| Autor: | Sekouba Keita, Roly Gosling, Halimatou Diawara, Kjerstin Lanke, Helmi Pett, Fanta Koita, Alassane Dicko, Eugenie Poirot, François Nosten, Sekou F. Traore, Mikko Niemi, Almahamoudou Mahamar, Koualy Sanogo, Harouna M Soumare, Jimee Hwang, Ingrid Chen, Charles E. McCulloch, Teun Bousema, Ibrahima Baber, Joelle Brown |
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| Přispěvatelé: | Clinicum, Department of Clinical Pharmacology, Medicum |
| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
Primaquine CLEARANCE medicine.medical_treatment CHILDREN Pharmacology Mali law.invention GAMETOCYTES Dihydroartemisinin/piperaquine Randomized controlled trial law Medicine Single-Blind Method Malaria Falciparum Artemisinin biology Artemisinins 3. Good health G6PD DEFICIENCY FEMALE Infectious Diseases SAFETY Quinolines Drug Therapy Combination medicine.drug AFRICA medicine.medical_specialty 030106 microbiology Dihydroartemisinin Drug Administration Schedule Antimalarials 03 medical and health sciences Internal medicine Piperaquine Anopheles parasitic diseases Animals Humans DIHYDROARTEMISININ-PIPERAQUINE business.industry Plasmodium falciparum QUANTIFICATION biology.organism_classification medicine.disease lnfectious Diseases and Global Health Radboud Institute for Health Sciences [Radboudumc 4] 3121 General medicine internal medicine and other clinical medicine business Malaria RESPONSES |
| Zdroj: | Lancet Infectious Diseases, 16, 6, pp. 674-84 The Lancet Infectious Diseases Lancet Infectious Diseases, 16, 674-84 |
| ISSN: | 1473-3099 |
| Popis: | Background Single low doses of primaquine, when added to artemisinin-based combination therapy, might prevent transmission of Plasmodium falciparum malaria to mosquitoes. We aimed to establish the activity and safety of four low doses of primaquine combined with dihydroartemisinin–piperaquine in male patients in Mali. Methods In this phase 2, single-blind, dose-ranging, adaptive randomised trial, we enrolled boys and men with uncomplicated P falciparum malaria at the Malaria Research and Training Centre (MRTC) field site in Ouelessebougou, Mali. All participants were confirmed positive carriers of gametocytes through microscopy and had normal function of glucose-6-phosphate dehydrogenase (G6PD) on colorimetric quantification. In the first phase, participants were randomly assigned (1:1:1) to one of three primaquine doses: 0 mg/kg (control), 0·125 mg/kg, and 0·5 mg/kg. Randomisation was done with a computer-generated randomisation list (in block sizes of six) and concealed with sealed, opaque envelopes. In the second phase, different participants were sequentially assigned (1:1) to 0·25 mg/kg primaquine or 0·0625 mg/kg primaquine. Primaquine tablets were dissolved into a solution and administered orally in a single dose. Participants were also given a 3 day course of dihydroartemisinin–piperaquine, administered by weight (320 mg dihydroartemisinin and 40 mg piperaquine per tablet). Outcome assessors were masked to treatment allocation, but participants were permitted to find out group assignment. Infectivity was assessed through membrane-feeding assays, which were optimised through the beginning part of phase one. The primary efficacy endpoint was the mean within-person percentage change in mosquito infectivity 2 days after primaquine treatment in participants who completed the study after optimisation of the infectivity assay, had both a pre-treatment infectivity measurement and at least one follow-up infectivity measurement, and who were given the correct primaquine dose. The safety endpoint was the mean within-person change in haemoglobin concentration during 28 days of study follow-up in participants with at least one follow-up visit. This study is registered with ClinicalTrials.gov, number NCT01743820. Findings Between Jan 2, 2013, and Nov 27, 2014, we enrolled 81 participants. In the primary analysis sample (n=71), participants in the 0·25 mg/kg primaquine dose group (n=15) and 0·5 mg/kg primaquine dose group (n=14) had significantly lower mean within-person reductions in infectivity at day 2—92·6% (95% CI 78·3–100; p=0·0014) for the 0·25 mg/kg group; and 75·0% (45·7–100; p=0·014) for the 0·5 mg/kg primaquine group—compared with those in the control group (n=14; 11·3% [–27·4 to 50·0]). Reductions were not significantly different from control for participants assigned to the 0·0625 mg/kg dose group (n=16; 41·9% [1·4–82·5]; p=0·16) and the 0·125 mg/kg dose group (n=12; 54·9% [13·4–96·3]; p=0·096). No clinically meaningful or statistically significant drops in haemoglobin were recorded in any individual in the haemoglobin analysis (n=70) during follow-up. No serious adverse events were reported and adverse events did not differ between treatment groups. Interpretation A single dose of 0·25 mg/kg primaquine, given alongside dihydroartemisinin–piperaquine, was safe and efficacious for the prevention of P falciparum malaria transmission in boys and men who are not deficient in G6PD. Future studies should assess the safety of single-dose primaquine in G6PD-deficient individuals to define the therapeutic range of primaquine to enable the safe roll-out of community interventions with primaquine. Funding Bill & Melinda Gates Foundation. |
| Databáze: | OpenAIRE |
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