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Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial

BACKGROUND: The emergence of artemisinin resistance has raised concerns that the most potent antimalarial drug may be under threat. The currently recommended daily dose of artesunate (AS) is 4 mg/kg, and is administered for 3 days together with a partner antimalarial drug. This study investigated th...

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Autores principales: Bethell, Delia, Se, Youry, Lon, Chanthap, Tyner, Stuart, Saunders, David, Sriwichai, Sabaithip, Darapiseth, Sea, Teja-Isavadharm, Paktiya, Khemawoot, Phisit, Schaecher, Kurt, Ruttvisutinunt, Wiriya, Lin, Jessica, Kuntawungin, Worachet, Gosi, Panita, Timmermans, Ans, Smith, Bryan, Socheat, Duong, Fukuda, Mark M.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3094355/
https://www.ncbi.nlm.nih.gov/pubmed/21603629
http://dx.doi.org/10.1371/journal.pone.0019283
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author Bethell, Delia
Se, Youry
Lon, Chanthap
Tyner, Stuart
Saunders, David
Sriwichai, Sabaithip
Darapiseth, Sea
Teja-Isavadharm, Paktiya
Khemawoot, Phisit
Schaecher, Kurt
Ruttvisutinunt, Wiriya
Lin, Jessica
Kuntawungin, Worachet
Gosi, Panita
Timmermans, Ans
Smith, Bryan
Socheat, Duong
Fukuda, Mark M.
author_facet Bethell, Delia
Se, Youry
Lon, Chanthap
Tyner, Stuart
Saunders, David
Sriwichai, Sabaithip
Darapiseth, Sea
Teja-Isavadharm, Paktiya
Khemawoot, Phisit
Schaecher, Kurt
Ruttvisutinunt, Wiriya
Lin, Jessica
Kuntawungin, Worachet
Gosi, Panita
Timmermans, Ans
Smith, Bryan
Socheat, Duong
Fukuda, Mark M.
author_sort Bethell, Delia
collection PubMed
description BACKGROUND: The emergence of artemisinin resistance has raised concerns that the most potent antimalarial drug may be under threat. The currently recommended daily dose of artesunate (AS) is 4 mg/kg, and is administered for 3 days together with a partner antimalarial drug. This study investigated the impact of different AS doses on clinical and parasitological responses in malaria patients from an area of known artemisinin resistance in western Cambodia. METHODS: Adult patients with uncomplicated P. falciparum malaria were randomized into one of three 7-day AS monotherapy regimens: 2, 4 or 6 mg/kg/day (total dose 14, 28 and 42 mg/kg). Clinical, parasitological, pharmacokinetic and in vitro drug sensitivity data was collected over a 7-day inpatient period and during weekly follow-up to 42 days. RESULTS: 143 patients were enrolled (n = 75, 40 and 28 to receive AS 2, 4 and 6 mg/kg/day respectively). Cure rates were high in all treatment groups at 42 days despite almost half the patients remaining parasitemic on Day 3. There was no impact of increasing AS dose on median parasite clearance times, median parasite clearance rates or on the proportion of patients remaining parasitemic on Day 3. However at the lowest dose used (2 mg/kg/d) patients with parasitemia >10,000/µL had longer median (IQR) parasite clearance times than those with parasitemia <10,000/µL (63 (48–75) vs. 84 (66–96) hours, p<0.0001). 19% of patients in the high-dose arm developed neutropenia (absolute neutrophil count <1.0×10(9)/L) by Day 14 and resulted in the arm being halted early. CONCLUSION: There is no pharmacodynamic benefit of increasing the daily dose of AS (4mg/kg) currently recommended for short-course combination treatment of uncomplicated malaria, even in regions with emerging artemisinin resistance, as long as the partner drug retains high efficacy. TRIAL REGISTRATION: ClinicalTrials.gov NCT00722150.
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spelling pubmed-30943552011-05-19 Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial Bethell, Delia Se, Youry Lon, Chanthap Tyner, Stuart Saunders, David Sriwichai, Sabaithip Darapiseth, Sea Teja-Isavadharm, Paktiya Khemawoot, Phisit Schaecher, Kurt Ruttvisutinunt, Wiriya Lin, Jessica Kuntawungin, Worachet Gosi, Panita Timmermans, Ans Smith, Bryan Socheat, Duong Fukuda, Mark M. PLoS One Research Article BACKGROUND: The emergence of artemisinin resistance has raised concerns that the most potent antimalarial drug may be under threat. The currently recommended daily dose of artesunate (AS) is 4 mg/kg, and is administered for 3 days together with a partner antimalarial drug. This study investigated the impact of different AS doses on clinical and parasitological responses in malaria patients from an area of known artemisinin resistance in western Cambodia. METHODS: Adult patients with uncomplicated P. falciparum malaria were randomized into one of three 7-day AS monotherapy regimens: 2, 4 or 6 mg/kg/day (total dose 14, 28 and 42 mg/kg). Clinical, parasitological, pharmacokinetic and in vitro drug sensitivity data was collected over a 7-day inpatient period and during weekly follow-up to 42 days. RESULTS: 143 patients were enrolled (n = 75, 40 and 28 to receive AS 2, 4 and 6 mg/kg/day respectively). Cure rates were high in all treatment groups at 42 days despite almost half the patients remaining parasitemic on Day 3. There was no impact of increasing AS dose on median parasite clearance times, median parasite clearance rates or on the proportion of patients remaining parasitemic on Day 3. However at the lowest dose used (2 mg/kg/d) patients with parasitemia >10,000/µL had longer median (IQR) parasite clearance times than those with parasitemia <10,000/µL (63 (48–75) vs. 84 (66–96) hours, p<0.0001). 19% of patients in the high-dose arm developed neutropenia (absolute neutrophil count <1.0×10(9)/L) by Day 14 and resulted in the arm being halted early. CONCLUSION: There is no pharmacodynamic benefit of increasing the daily dose of AS (4mg/kg) currently recommended for short-course combination treatment of uncomplicated malaria, even in regions with emerging artemisinin resistance, as long as the partner drug retains high efficacy. TRIAL REGISTRATION: ClinicalTrials.gov NCT00722150. Public Library of Science 2011-05-13 /pmc/articles/PMC3094355/ /pubmed/21603629 http://dx.doi.org/10.1371/journal.pone.0019283 Text en Bethell et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bethell, Delia
Se, Youry
Lon, Chanthap
Tyner, Stuart
Saunders, David
Sriwichai, Sabaithip
Darapiseth, Sea
Teja-Isavadharm, Paktiya
Khemawoot, Phisit
Schaecher, Kurt
Ruttvisutinunt, Wiriya
Lin, Jessica
Kuntawungin, Worachet
Gosi, Panita
Timmermans, Ans
Smith, Bryan
Socheat, Duong
Fukuda, Mark M.
Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial
title Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial
title_full Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial
title_fullStr Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial
title_full_unstemmed Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial
title_short Artesunate Dose Escalation for the Treatment of Uncomplicated Malaria in a Region of Reported Artemisinin Resistance: A Randomized Clinical Trial
title_sort artesunate dose escalation for the treatment of uncomplicated malaria in a region of reported artemisinin resistance: a randomized clinical trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3094355/
https://www.ncbi.nlm.nih.gov/pubmed/21603629
http://dx.doi.org/10.1371/journal.pone.0019283
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