A multicentre, randomised, non-inferiority clinical trial comparing a nifurtimox-eflornithine combination to standard eflornithine monotherapy for late stage Trypanosoma brucei gambiense human African trypanosomiasis in Uganda

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dc.contributor.author Kansiime, Freddie
dc.contributor.author Adibaku, Seraphine
dc.contributor.author Wamboga, Charles
dc.contributor.author Franklin, Idi
dc.contributor.author Drago Kato, Charles
dc.contributor.author Yamuah, Lawrence
dc.contributor.author Vaillant, Michel
dc.contributor.author Kioy, Deborah
dc.contributor.author Olliaro, Piero
dc.contributor.author Matovu, Enock
dc.date.accessioned 2018-12-17T15:34:36Z
dc.date.available 2018-12-17T15:34:36Z
dc.date.issued 2018
dc.identifier.uri DOI 10.1186/s13071-018-2634-x
dc.identifier.uri http://hdl.handle.net/20.500.12283/154
dc.description.abstract Background: While the combination of nifurtimox and eflornithine (NECT) is currently recommended for the treatment of the late stage human African trypansomiasis (HAT), single-agent eflornithine was still the treatment of choice when this trial commenced. This study intended to provide supportive evidence to complement previous trials. Methods: A multi-centre randomised, open-label, non-inferiority trial was carried out in the Trypanosoma brucei gambiense endemic districts of North-Western Uganda to compare the efficacy and safety of NECT (200 mg/kg eflornithine infusions every 12 h for 7 days and 8 hourly oral nifurtimox at 5 mg/kg for 10 days) to the standard eflornithine regimen (6 hourly at 100 mg/kg for 14 days). The primary endpoint was the cure rate, determined as the proportion of patients alive and without laboratory signs of infection at 18 months post-treatment, with no demonstrated trypanosomes in the cerebrospinal fluid (CSF), blood or lymph node aspirates, and CSF white blood cell count < 20 /μl. The non-inferiority margin was set at 10%. Results: One hundred and nine patients were enrolled; all contributed to the intent-to-treat (ITT), modified intent-to-treat (mITT) and safety populations, while 105 constituted the per-protocol population (PP). The cure rate was 90.9% for NECT and 88.9% for eflornithine in the ITT and mITT populations; the same was 90.6 and 88.5%, respectively in the PP population. Non-inferiority was demonstrated for NECT in all populations: differences in cure rates were 0.02 (95% CI: -0.07–0.11) and 0.02 (95% CI: -0.08–0.12) respectively. Two patients died while on treatment (1 in each arm), and 3 more during follow-up in the NECT arm. No difference was found between the two arms for the secondary efficacy and safety parameters. A meta-analysis involving several studies demonstrated non-inferiority of NECT to eflornithine monotherapy. (Continued on next page) en_US
dc.language.iso en en_US
dc.publisher Springer Nature en_US
dc.subject Human African trypanosomiasis (HAT), en_US
dc.subject Nifurtimox-eflornithine combination treatment (NECT) en_US
dc.subject Second-stage HAT en_US
dc.subject Meningo-encephalitic stage en_US
dc.subject Human African trypanosomiasis (HAT) en_US
dc.title A multicentre, randomised, non-inferiority clinical trial comparing a nifurtimox-eflornithine combination to standard eflornithine monotherapy for late stage Trypanosoma brucei gambiense human African trypanosomiasis in Uganda en_US
dc.title.alternative Parasites & vectors en_US
dc.type Article en_US


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