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 |