| 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 |