Development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria

Abstract Background In many endemic areas, Plasmodium vivax malaria is predominantly a disease of young adults and children. International recommendations for radical cure recommend fixed target doses of 0.25 or 0.5 mg/kg/day of primaquine for 14 days in glucose-6-phosphate dehydrogenase normal pati...

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Main Authors: Walter Robert Taylor, Richard M. Hoglund, Pimnara Peerawaranun, Thuy Nhien Nguyen, Tran Tinh Hien, Arnaud Tarantola, Lorenz von Seidlein, Rupam Tripura, Thomas J. Peto, Arjen M. Dondorp, Jordi Landier, Francois H.Nosten, Frank Smithuis, Koukeo Phommasone, Mayfong Mayxay, Soy Ty Kheang, Chy Say, Kak Neeraj, Leang Rithea, Lek Dysoley, Sim Kheng, Sinoun Muth, Arantxa Roca-Feltrer, Mark Debackere, Rick M. Fairhurst, Ngak Song, Philippe Buchy, Didier Menard, Nicholas J. White, Joel Tarning, Mavuto Mukaka
Format: Article
Language:English
Published: BMC 2021-09-01
Series:Malaria Journal
Subjects:
Online Access:https://doi.org/10.1186/s12936-021-03886-w
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language English
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author Walter Robert Taylor
Richard M. Hoglund
Pimnara Peerawaranun
Thuy Nhien Nguyen
Tran Tinh Hien
Arnaud Tarantola
Lorenz von Seidlein
Rupam Tripura
Thomas J. Peto
Arjen M. Dondorp
Jordi Landier
Francois H.Nosten
Frank Smithuis
Koukeo Phommasone
Mayfong Mayxay
Soy Ty Kheang
Chy Say
Kak Neeraj
Leang Rithea
Lek Dysoley
Sim Kheng
Sinoun Muth
Arantxa Roca-Feltrer
Mark Debackere
Rick M. Fairhurst
Ngak Song
Philippe Buchy
Didier Menard
Nicholas J. White
Joel Tarning
Mavuto Mukaka
spellingShingle Walter Robert Taylor
Richard M. Hoglund
Pimnara Peerawaranun
Thuy Nhien Nguyen
Tran Tinh Hien
Arnaud Tarantola
Lorenz von Seidlein
Rupam Tripura
Thomas J. Peto
Arjen M. Dondorp
Jordi Landier
Francois H.Nosten
Frank Smithuis
Koukeo Phommasone
Mayfong Mayxay
Soy Ty Kheang
Chy Say
Kak Neeraj
Leang Rithea
Lek Dysoley
Sim Kheng
Sinoun Muth
Arantxa Roca-Feltrer
Mark Debackere
Rick M. Fairhurst
Ngak Song
Philippe Buchy
Didier Menard
Nicholas J. White
Joel Tarning
Mavuto Mukaka
Development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria
Malaria Journal
Primaquine
Allometric scaling
Age-based dosing
Weight-based dosing
Plasmodium vivax
author_facet Walter Robert Taylor
Richard M. Hoglund
Pimnara Peerawaranun
Thuy Nhien Nguyen
Tran Tinh Hien
Arnaud Tarantola
Lorenz von Seidlein
Rupam Tripura
Thomas J. Peto
Arjen M. Dondorp
Jordi Landier
Francois H.Nosten
Frank Smithuis
Koukeo Phommasone
Mayfong Mayxay
Soy Ty Kheang
Chy Say
Kak Neeraj
Leang Rithea
Lek Dysoley
Sim Kheng
Sinoun Muth
Arantxa Roca-Feltrer
Mark Debackere
Rick M. Fairhurst
Ngak Song
Philippe Buchy
Didier Menard
Nicholas J. White
Joel Tarning
Mavuto Mukaka
author_sort Walter Robert Taylor
title Development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria
title_short Development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria
title_full Development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria
title_fullStr Development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria
title_full_unstemmed Development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria
title_sort development of weight and age-based dosing of daily primaquine for radical cure of vivax malaria
publisher BMC
series Malaria Journal
issn 1475-2875
publishDate 2021-09-01
description Abstract Background In many endemic areas, Plasmodium vivax malaria is predominantly a disease of young adults and children. International recommendations for radical cure recommend fixed target doses of 0.25 or 0.5 mg/kg/day of primaquine for 14 days in glucose-6-phosphate dehydrogenase normal patients of all ages. However, for many anti-malarial drugs, including primaquine, there is evidence that children have lower exposures than adults for the same weight-adjusted dose. The aim of the study was to develop 14-day weight-based and age-based primaquine regimens against high-frequency relapsing tropical P. vivax. Methods The recommended adult target dose of 0.5 mg/kg/day (30 mg in a 60 kg patient) is highly efficacious against tropical P. vivax and was assumed to produce optimal drug exposure. Primaquine doses were calculated using allometric scaling to derive a weight-based primaquine regimen over a weight range from 5 to 100 kg. Growth curves were constructed from an anthropometric database of 53,467 individuals from the Greater Mekong Subregion (GMS) to define weight-for-age relationships. The median age associated with each weight was used to derive an age-based dosing regimen from the weight-based regimen. Results The proposed weight-based regimen has 5 dosing bands: (i) 5–7 kg, 5 mg, resulting in 0.71–1.0 mg/kg/day; (ii) 8–16 kg, 7.5 mg, 0.47–0.94 mg/kg/day; (iii) 17–40 kg, 15 mg, 0.38–0.88 mg/kg/day; (iv) 41–80 kg, 30 mg, 0.37–0.73 mg/kg/day; and (v) 81–100 kg, 45 mg, 0.45–0.56 mg/kg/day. The corresponding age-based regimen had 4 dosing bands: 6–11 months, 5 mg, 0.43–1.0 mg/kg/day; (ii) 1–5 years, 7.5 mg, 0.35–1.25 mg/kg/day; (iii) 6–14 years, 15 mg, 0.30–1.36 mg/kg/day; and (iv) ≥ 15 years, 30 mg, 0.35–1.07 mg/kg/day. Conclusion The proposed weight-based regimen showed less variability around the primaquine dose within each dosing band compared to the age-based regimen and is preferred. Increased dose accuracy could be achieved by additional dosing bands for both regimens. The age-based regimen might not be applicable to regions outside the GMS, which must be based on local anthropometric data. Pharmacokinetic data in small children are needed urgently to inform the proposed regimens.
topic Primaquine
Allometric scaling
Age-based dosing
Weight-based dosing
Plasmodium vivax
url https://doi.org/10.1186/s12936-021-03886-w
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spelling doaj-99fc57599ac04492ad2d3235bd20aa6f2021-09-12T11:43:23ZengBMCMalaria Journal1475-28752021-09-0120111010.1186/s12936-021-03886-wDevelopment of weight and age-based dosing of daily primaquine for radical cure of vivax malariaWalter Robert Taylor0Richard M. Hoglund1Pimnara Peerawaranun2Thuy Nhien Nguyen3Tran Tinh Hien4Arnaud Tarantola5Lorenz von Seidlein6Rupam Tripura7Thomas J. Peto8Arjen M. Dondorp9Jordi Landier10Francois H.Nosten11Frank Smithuis12Koukeo Phommasone13Mayfong Mayxay14Soy Ty Kheang15Chy Say16Kak Neeraj17Leang Rithea18Lek Dysoley19Sim Kheng20Sinoun Muth21Arantxa Roca-Feltrer22Mark Debackere23Rick M. Fairhurst24Ngak Song25Philippe Buchy26Didier Menard27Nicholas J. White28Joel Tarning29Mavuto Mukaka30Mahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityOxford University Clinical Research Unit, Wellcome Trust Major Oversea ProgrammeCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of OxfordInstitut Pasteur du CambodgeMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityShoklo Malaria Research UnitCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of OxfordMyanmar Oxford Clinical Research UnitLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Mahosot HospitalLao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Mahosot HospitalCenter for Health and Social Development (HSD), National Institute for Public Health (NIPH) and University Research Co., LLC (URC)Center for Health and Social Development (HSD), National Institute for Public Health (NIPH) and University Research Co., LLC (URC)University Research Co., LLC Washington DCNational Center for Parasitology, Entomology and Malaria ControlNational Center for Parasitology, Entomology and Malaria ControlNational Center for Parasitology, Entomology and Malaria ControlNational Center for Parasitology, Entomology and Malaria ControlMalaria ConsortiumMSF Belgium Cambodia Malaria ProgramLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of HealthFHI 360 Cambodia Office, Keng Kang III Khan ChamkamonInstitut Pasteur du CambodgeInstitut Pasteur du CambodgeMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityMahidol Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol UniversityAbstract Background In many endemic areas, Plasmodium vivax malaria is predominantly a disease of young adults and children. International recommendations for radical cure recommend fixed target doses of 0.25 or 0.5 mg/kg/day of primaquine for 14 days in glucose-6-phosphate dehydrogenase normal patients of all ages. However, for many anti-malarial drugs, including primaquine, there is evidence that children have lower exposures than adults for the same weight-adjusted dose. The aim of the study was to develop 14-day weight-based and age-based primaquine regimens against high-frequency relapsing tropical P. vivax. Methods The recommended adult target dose of 0.5 mg/kg/day (30 mg in a 60 kg patient) is highly efficacious against tropical P. vivax and was assumed to produce optimal drug exposure. Primaquine doses were calculated using allometric scaling to derive a weight-based primaquine regimen over a weight range from 5 to 100 kg. Growth curves were constructed from an anthropometric database of 53,467 individuals from the Greater Mekong Subregion (GMS) to define weight-for-age relationships. The median age associated with each weight was used to derive an age-based dosing regimen from the weight-based regimen. Results The proposed weight-based regimen has 5 dosing bands: (i) 5–7 kg, 5 mg, resulting in 0.71–1.0 mg/kg/day; (ii) 8–16 kg, 7.5 mg, 0.47–0.94 mg/kg/day; (iii) 17–40 kg, 15 mg, 0.38–0.88 mg/kg/day; (iv) 41–80 kg, 30 mg, 0.37–0.73 mg/kg/day; and (v) 81–100 kg, 45 mg, 0.45–0.56 mg/kg/day. The corresponding age-based regimen had 4 dosing bands: 6–11 months, 5 mg, 0.43–1.0 mg/kg/day; (ii) 1–5 years, 7.5 mg, 0.35–1.25 mg/kg/day; (iii) 6–14 years, 15 mg, 0.30–1.36 mg/kg/day; and (iv) ≥ 15 years, 30 mg, 0.35–1.07 mg/kg/day. Conclusion The proposed weight-based regimen showed less variability around the primaquine dose within each dosing band compared to the age-based regimen and is preferred. Increased dose accuracy could be achieved by additional dosing bands for both regimens. The age-based regimen might not be applicable to regions outside the GMS, which must be based on local anthropometric data. Pharmacokinetic data in small children are needed urgently to inform the proposed regimens.https://doi.org/10.1186/s12936-021-03886-wPrimaquineAllometric scalingAge-based dosingWeight-based dosingPlasmodium vivax