Evidence map›Paper›PMID 25075834›Full record

Trial reportThe New England journal of medicine2014

Spread of artemisinin resistance in Plasmodium falciparum malaria.

Elizabeth A Ashley, Mehul Dhorda, Rick M Fairhurst, Chanaki Amaratunga, Parath Lim, Seila Suon, Sokunthea Sreng, Jennifer M Anderson, Sivanna Mao, Baramey Sam and 74 more

Erratum issued 2 registry-linked trialsOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The New England journal of medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 2 registered trials, which are not on this map. Cited by 1,286 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,286citing papers in PubMed, 2 pooled it
226.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01350856 phase4completednot on this map

A Multicentre, Randomised Trial to Detect in Vivo Resistance of Plasmodium Falciparum to Artesunate in Patients With Uncomplicated Malaria.

TypeinterventionalSponsorUniversity of OxfordRan2011 to 2014Enrolled1,700ConditionsFalciparum MalariaArmsArtesunate 2, Artesunate 4
NCT02612545 phase1completednot on this mapstarted 2015, after this paper: background citation

A Multi-Site, Open-Label, Randomized Trial to Assess the Efficacy, Safety, and Tolerability of Dihydroartemisinin-Piperaquine Plus Mefloquine Compared to Dihydroartemisinin-Piperaquine or Artesunate-Mefloquine in Patients With Uncomplicated Falciparum Malaria in Cambodia

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2015 to 2019Enrolled216ConditionsAcute Falciparum MalariaArmsDihydroartemisinin-piperaquine (DHA-PPQ), Mefloquine (MQ)
3 · Its place in the literature

Who cites it

1,286 citing papers in PubMed, 2 syntheses or guidelines pooled it, 2,201 citations in OpenAlex.

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1,226 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

84 authors at 20 institutions in 13 countries.

Elizabeth A AshleyThe authors' affiliations are listed in the Appendix.
Mehul Dhorda
Rick M Fairhurst
Chanaki Amaratunga
Parath Lim
Seila Suon
Sokunthea Sreng
Jennifer M Anderson
Sivanna Mao
Baramey Sam
Chantha Sopha
Char Meng Chuor
Chea Nguon
Siv Sovannaroth
Sasithon Pukrittayakamee
Podjanee Jittamala
Kesinee Chotivanich
Kitipumi Chutasmit
Chaiyaporn Suchatsoonthorn
Ratchadaporn Runcharoen
Tran Tinh Hien
Nguyen Thanh Thuy-Nhien
Ngo Viet Thanh
Nguyen Hoan Phu
Ye Htut
Kay-Thwe Han
Kyin Hla Aye
Olugbenga A Mokuolu
Rasaq R Olaosebikan
Olaleke O Folaranmi
Mayfong Mayxay
Maniphone Khanthavong
Bouasy Hongvanthong
Paul N Newton
Marie A Onyamboko
Caterina I Fanello
Antoinette K Tshefu
Neelima Mishra
Neena Valecha
Aung Pyae Phyo
Francois Nosten
Poravuth Yi
Rupam Tripura
Steffen Borrmann
Mahfudh Bashraheil
Judy Peshu
M Abul Faiz
Aniruddha Ghose
M Amir Hossain
Rasheda Samad
M Ridwanur Rahman
M Mahtabuddin Hasan
Akhterul Islam
Olivo Miotto
Roberto Amato
Bronwyn MacInnis
Jim Stalker
Dominic P Kwiatkowski
Zbynek Bozdech
Atthanee Jeeyapant
Phaik Yeong Cheah
Tharisara Sakulthaew
Jeremy Chalk
Benjamas Intharabut
Kamolrat Silamut
Sue J Lee
Benchawan Vihokhern
Chanon Kunasol
Mallika Imwong
Joel Tarning
Walter J Taylor
Shunmay Yeung
Charles J Woodrow
Jennifer A Flegg
Debashish Das
Jeffery Smith
Meera Venkatesan
Christopher V Plowe
Kasia Stepniewska
Philippe J Guerin
Arjen M Dondorp
Nicholas P Day
Nicholas J White
Tracking Resistance to Artemisinin Collaboration (TRAC)
Hospital for Tropical Diseases · VNMahidol Oxford Tropical Medicine Research Unit · THCambodia National Malaria Center · KHUniversity of Tübingen · DEMyanmar Oxford Clinical Research Unit · MMOxford University Clinical Research Unit · VNUniversity of Maryland, Baltimore · USIld Care Foundation · NLKenya Medical Research Institute · KENational Institute of Allergy and Infectious Diseases · USNational Institute of Malaria Research · INShoklo Malaria Research Unit · THUniversity of Oxford · GBWellcome Sanger Institute · GBCentre for Human Genetics · GBFaculty of Public Health · GBMahidol University · THMinistry of Public Health · CDNanyang Technological University · SGNational Institutes of Health · US

Funding

International Research in Cambodia: Tropical Medicine and Vector Research ZIAAI001066 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI YEK, CHRISTINA · 2009 to 2025
$10.8M
Malaria Pathogenesis and Human ImmunityZIAAI001000 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FAIRHURST, RICK · 2009 to 2017
$9.3M
Intramural NIH HHSWellcome Trust 077166Wellcome Trust 090532Wellcome Trust 090770Wellcome Trust 093956
6 · The paper itself

Abstract

backgroundArtemisinin resistance in Plasmodium falciparum has emerged in Southeast Asia and now poses a threat to the control and elimination of malaria. Mapping the geographic extent of resistance is essential for planning containment and elimination strategies.

methodsBetween May 2011 and April 2013, we enrolled 1241 adults and children with acute, uncomplicated falciparum malaria in an open-label trial at 15 sites in 10 countries (7 in Asia and 3 in Africa). Patients received artesunate, administered orally at a daily dose of either 2 mg per kilogram of body weight per day or 4 mg per kilogram, for 3 days, followed by a standard 3-day course of artemisinin-based combination therapy. Parasite counts in peripheral-blood samples were measured every 6 hours, and the parasite clearance half-lives were determined.

resultsThe median parasite clearance half-lives ranged from 1.9 hours in the Democratic Republic of Congo to 7.0 hours at the Thailand-Cambodia border. Slowly clearing infections (parasite clearance half-life >5 hours), strongly associated with single point mutations in the "propeller" region of the P. falciparum kelch protein gene on chromosome 13 (kelch13), were detected throughout mainland Southeast Asia from southern Vietnam to central Myanmar. The incidence of pretreatment and post-treatment gametocytemia was higher among patients with slow parasite clearance, suggesting greater potential for transmission. In western Cambodia, where artemisinin-based combination therapies are failing, the 6-day course of antimalarial therapy was associated with a cure rate of 97.7% (95% confidence interval, 90.9 to 99.4) at 42 days.

conclusionsArtemisinin resistance to P. falciparum, which is now prevalent across mainland Southeast Asia, is associated with mutations in kelch13. Prolonged courses of artemisinin-based combination therapies are currently efficacious in areas where standard 3-day treatments are failing. (Funded by the U.K. Department of International Development and others; ClinicalTrials.gov number, NCT01350856.).

Indexed as

AdolescentAdultAfrica South of the SaharaAntimalarialsArtemisininsAsia, SoutheasternChildChild, PreschoolDrug ResistanceHumansInfantMalaria, FalciparumMiddle AgedMultivariate AnalysisParasite LoadParasitemiaAntimalarialsArtemisininsProtozoan Proteins

Identifiers

PMID25075834
PMCPMC4143591
OpenAlexW2171102256

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.