Background: Human African trypanosomiasis caused by Trypanosoma brucei gambiense is a fatal disease. Current treatment options for patients with second-stage disease are either highly toxic or impracticable in field conditions. We compared the efficacy and safety of the nifurtimox-eflornithine drug combination with the standard eflornithine regimen for the treatment of second-stage disease.

Methods: A randomized, open-label, active-control, phase III clinical trial comparing 2 arms was conducted at the Sleeping Sickness Treatment Center, which was run by Medecins Sans Frontieres, in Nkayi, Bouenza Province, Republic of Congo. Patients were screened for inclusion and randomly assigned to receive eflornithine alone (400 mg/kg per day given intravenously every 6 h for 14 days) or eflornithine (400 mg/kg per day given intravenously every 12 h for 7 days) plus nifurtimox (15 mg/kg per day given orally every 8 h for 10 days). Patients were observed for 18 months. The study's outcomes were cure and adverse events attributable to treatment.

Results: A total of 103 patients with second-stage disease were enrolled. Cure rates were 94.1% for the eflornithine group and 96.2% for the nifurtimox-eflornithine group. Drug reactions were frequent in both arms, and severe reactions affected 25.5% of patients in the eflornithine group and 9.6% of those in the nifurtimox-eflornithine group, resulting in 2 and 1 treatment suspensions, respectively. There was 1 death in the eflornithine arm and no deaths in the nifurtimox-eflornithine arm.

Conclusions: The nifurtimox-eflornithine combination appears to be a promising first-line therapy for second-stage sleeping sickness. If our findings are corroborated by ongoing findings from additional sites (a multicenter extension of this study), the new nifurtimox-eflornithine combination therapy will mark a major and multifaceted advance over current therapies.

Download full-text PDF

Source
http://dx.doi.org/10.1086/522982DOI Listing

Publication Analysis

Top Keywords

nifurtimox-eflornithine combination
12
sleeping sickness
12
mg/kg day
12
combination therapy
8
therapy second-stage
8
trypanosoma brucei
8
brucei gambiense
8
clinical trial
8
patients second-stage
8
second-stage disease
8

Similar Publications

Transforming the chemotherapy of human African trypanosomiasis.

Clin Microbiol Rev

January 2025

School of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom.

SUMMARYPrior to 2019, when the orally available drug fexinidazole began its clinical use, the treatment of human African trypanosomiasis (HAT) was complex and unsatisfactory for many reasons. Two sub-species of the parasite are responsible for HAT, namely the rhodesiense form found in East and Southern Africa and the gambiense form found in Central and West Africa. Diseases caused by both forms manifest in two stages: stage 1 before and stage 2 after central nervous system involvement.

View Article and Find Full Text PDF

The evolving spectrum of human African trypanosomiasis.

QJM

June 2024

School of Psychology and Neuroscience, College of Medical, Veterinary and Life Sciences, University of Glasgow, Wellcome Surgical Institute, Garscube Campus, Glasgow G61 1QH, UK.

Article Synopsis
  • Human African trypanosomiasis (HAT), or sleeping sickness, poses a significant health threat in 36 sub-Saharan African countries, affecting up to 60 million people, but recent efforts have led to a dramatic decline in cases.
  • Improved diagnostic methods and treatment options, such as the nifurtimox-eflornithine combination therapy (NECT) and oral fexinidazole, have been developed, enhancing patient outcomes.
  • While the World Health Organization's initial goal of reducing HAT as a public health issue by 2020 has likely been met, achieving the more ambitious target of interrupting transmission by 2030 remains uncertain.
View Article and Find Full Text PDF

Background: Human African trypanosomiasis caused by Trypanosoma brucei gambiense (gambiense HAT) in patients with late-stage disease requires hospital admission to receive nifurtimox-eflornithine combination therapy (NECT). Fexinidazole, the latest treatment that has been recommended by WHO, also requires systematic admission to hospital, which is problematic in areas with few health-care resources. We aim to assess the safety and efficacy of acoziborole in adult and adolescent patients with gambiense HAT.

View Article and Find Full Text PDF

Systematic Review and Meta-Analysis on Human African Trypanocide Resistance.

Pathogens

September 2022

Infection Medicine, Deanery of Biomedical Sciences, Edinburgh Medical School, College of Medicine and Veterinary Medicine, The University of Edinburgh, Edinburgh EH8 9JZ, UK.

Background Human African trypanocide resistance (HATr) is a challenge for the eradication of Human African Trypansomiaisis (HAT) following the widespread emergence of increased monotherapy drug treatment failures against Trypanosoma brucei gambiense and T. b. rhodesiense that are associated with changes in pathogen receptors.

View Article and Find Full Text PDF

An Update on African Trypanocide Pharmaceutics and Resistance.

Front Vet Sci

March 2022

Infection Medicine, Deanery of Biomedical Sciences, College of Medicine and Veterinary Medicine, The University of Edinburgh, Edinburgh, United Kingdom.

African trypanosomiasis is associated with , and pathogens in African animal trypanosomiasis (AAT) while and are responsible for chronic and acute human African trypanosomiasis (HAT), respectively. Suramin sodium suppresses ATP generation during the glycolytic pathway and is ineffective against and infections. Resistance to suramin is associated with pathogen altered transport proteins.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!