Failure of artemether-lumefantrine therapy in travellers returning to Belgium with plasmodium falciparum malaria: an observational case series with genomic analysis.

artemisinin-based combination therapy drug resistance failure malaria genomic surveillance travel

Journal

Journal of travel medicine
ISSN: 1708-8305
Titre abrégé: J Travel Med
Pays: England
ID NLM: 9434456

Informations de publication

Date de publication:
29 Dec 2023
Historique:
medline: 2 1 2024
pubmed: 2 1 2024
entrez: 29 12 2023
Statut: aheadofprint

Résumé

Failure of artemisinin-based combination therapy (ACT) is increasingly reported in patients with Plasmodium falciparum malaria in sub-Saharan Africa. We aimed to describe the clinical and genomic characteristics of recent cases of P. falciparum malaria failing artemether-lumefantrine in Belgium. Travel-related cases of malaria confirmed at the national reference laboratory of the Institute of Tropical Medicine (ITM), Antwerp, Belgium, were reviewed. All cases for whom attending clinicians reported persistence (beyond Day 3 post-treatment initiation, i.e. early failure) or recrudescence (from Day 7 to 42, i.e. late failure) of P. falciparum parasites despite adequate drug intake were analysed. Both initial and persistent/recurrent samples were submitted to next generation sequencing to investigate resistance-conferring mutations. From July 2022 to June 2023, eight P. falciparum cases of failure with artemether-lumefantrine therapy were reported (early failure = 1; late failure = 7). All travellers were returning from sub-Saharan Africa, most (6/8) after a trip to visit friends and relatives. PfK13 mutations associated with resistance to artemisinin were found in two travellers returning from East Africa, including the validated marker R561H in the patient with early failure and the candidate marker A675V in a patient with late failure. Additional mutations were detected that could contribute to decreased susceptibility to artemisinin in another three cases, lumefantrine in six cases, and proguanil in all eight participants. Various regimens were used to treat the persistent/recrudescent cases, with favourable outcome. Within a 12-month period, we investigated eight travellers returning from sub-Saharan Africa with P. falciparum malaria and in whom artemether-lumefantrine failure was documented. Mutations conferring resistance to antimalarials were found in all analysed blood samples, especially against lumefantrine and proguanil, but also artemisinin. There is a pressing need for systematic genomic surveillance of resistance to antimalarials in international travellers with P. falciparum malaria, especially those experiencing treatment failure.

Sections du résumé

BACKGROUND BACKGROUND
Failure of artemisinin-based combination therapy (ACT) is increasingly reported in patients with Plasmodium falciparum malaria in sub-Saharan Africa. We aimed to describe the clinical and genomic characteristics of recent cases of P. falciparum malaria failing artemether-lumefantrine in Belgium.
METHODS METHODS
Travel-related cases of malaria confirmed at the national reference laboratory of the Institute of Tropical Medicine (ITM), Antwerp, Belgium, were reviewed. All cases for whom attending clinicians reported persistence (beyond Day 3 post-treatment initiation, i.e. early failure) or recrudescence (from Day 7 to 42, i.e. late failure) of P. falciparum parasites despite adequate drug intake were analysed. Both initial and persistent/recurrent samples were submitted to next generation sequencing to investigate resistance-conferring mutations.
RESULTS RESULTS
From July 2022 to June 2023, eight P. falciparum cases of failure with artemether-lumefantrine therapy were reported (early failure = 1; late failure = 7). All travellers were returning from sub-Saharan Africa, most (6/8) after a trip to visit friends and relatives. PfK13 mutations associated with resistance to artemisinin were found in two travellers returning from East Africa, including the validated marker R561H in the patient with early failure and the candidate marker A675V in a patient with late failure. Additional mutations were detected that could contribute to decreased susceptibility to artemisinin in another three cases, lumefantrine in six cases, and proguanil in all eight participants. Various regimens were used to treat the persistent/recrudescent cases, with favourable outcome.
CONCLUSION CONCLUSIONS
Within a 12-month period, we investigated eight travellers returning from sub-Saharan Africa with P. falciparum malaria and in whom artemether-lumefantrine failure was documented. Mutations conferring resistance to antimalarials were found in all analysed blood samples, especially against lumefantrine and proguanil, but also artemisinin. There is a pressing need for systematic genomic surveillance of resistance to antimalarials in international travellers with P. falciparum malaria, especially those experiencing treatment failure.

Identifiants

pubmed: 38157311
pii: 7503849
doi: 10.1093/jtm/taad165
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of International Society of Travel Medicine. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Jan Pierreux (J)

Infectious Diseases Department, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Emmanuel Bottieau (E)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Eric Florence (E)

Department of General Internal Medicine and infectious Diseases, Belgium, University Hospital of Antwerp, Belgium.

Ula Maniewski (U)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Anne Bruggemans (A)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Jiska Malotaux (J)

Department of General Internal Medicine and Infectious Diseases, Ghent University Hospital, Ghent, Belgium.

Charlotte Martin (C)

Infectious Diseases Department, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Janneke Cox (J)

Department of Infectious Diseases and Immunity, Jessa Hospital, Hasselt, Belgium.
Faculty of Medicine and Life Sciences, University of Hasselt, Belgium.

Deborah Konopnicki (D)

Infectious Diseases Department, Saint-Pierre University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Pieter Guetens (P)

Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Jacob Verschueren (J)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Jasmine Coppens (J)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Marjan Van Esbroeck (M)

Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Mathijs Mutsaers (M)

Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Anna Rosanas-Urgell (A)

Department of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.

Classifications MeSH