Three drug combinations for late-stage Trypanosoma brucei gambiense sleeping sickness: a randomized clinical trial in Uganda.

Gerardo Priotto, Carole Fogg, Manica Balasegaram, Olema Erphas, Albino Louga, Francesco Checchi, Salah Ghabri, Patrice Piola
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引用次数: 110

Abstract

Objectives: Our objective was to compare the efficacy and safety of three drug combinations for the treatment of late-stage human African trypanosomiasis caused by Trypanosoma brucei gambiense.

Design: This trial was a randomized, open-label, active control, parallel clinical trial comparing three arms.

Setting: The study took place at the Sleeping Sickness Treatment Center run by Médecins Sans Frontières at Omugo, Arua District, Uganda

Participants: Stage 2 patients diagnosed in Northern Uganda were screened for inclusion and a total of 54 selected.

Interventions: Three drug combinations were given to randomly assigned patients: melarsoprol-nifurtimox (M+N), melarsoprol-eflornithine (M+E), and nifurtimox-eflornithine (N+E). Dosages were uniform: intravenous (IV) melarsoprol 1.8 mg/kg/d, daily for 10 d; IV eflornithine 400 mg/kg/d, every 6 h for 7 d; oral nifurtimox 15 (adults) or 20 (children <15 y) mg/kg/d, every 8 h for 10 d. Patients were followed up for 24 mo.

Outcome measures: Outcomes were cure rates and adverse events attributable to treatment.

Results: Randomization was performed on 54 patients before enrollment was suspended due to unacceptable toxicity in one of the three arms. Cure rates obtained with the intention to treat analysis were M+N 44.4%, M+E 78.9%, and N+E 94.1%, and were significantly higher with N+E (p = 0.003) and M+E (p = 0.045) than with M+N. Adverse events were less frequent and less severe with N+E, resulting in fewer treatment interruptions and no fatalities. Four patients died who were taking melarsoprol-nifurtimox and one who was taking melarsoprol-eflornithine.

Conclusions: The N+E combination appears to be a promising first-line therapy that may improve treatment of sleeping sickness, although the results from this interrupted study do not permit conclusive interpretations. Larger studies are needed to continue the evaluation of this drug combination in the treatment of T. b. gambiense sleeping sickness.

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治疗晚期布氏锥虫冈比亚昏睡病的三种药物组合:乌干达的一项随机临床试验
目的:我们的目的是比较三种药物组合治疗由布氏冈比亚锥虫引起的晚期非洲人锥虫病的疗效和安全性。设计:该试验是一项随机、开放标签、主动对照、平行临床试验,比较三个组。环境:该研究在乌干达阿鲁阿区Omugo由无国界医生组织管理的昏睡病治疗中心进行。参与者:在乌干达北部诊断出的第二阶段患者进行了筛选,共选择了54人。干预措施:对随机分配的患者给予三种药物组合:美拉索prol-硝呋替莫(M+N)、美拉索prol-依氟鸟氨酸(M+E)和硝呋替莫-依氟鸟氨酸(N+E)。剂量一致:静脉滴注(IV)美拉胂醇1.8 mg/kg/d,每日,连用10 d;静脉注射异氟鸟氨酸400 mg/kg/d,每6 h一次,连用7 d;口服硝呋替莫15(成人)或20(儿童)。结果测量:结果是治愈率和治疗引起的不良事件。结果:54例患者进行了随机分组,然后由于其中一个组的不可接受的毒性而暂停入组。意向治疗分析获得的治愈率M+N为44.4%,M+E为78.9%,N+E为94.1%,且N+E组(p = 0.003)和M+E组(p = 0.045)显著高于M+N组。N+E组不良事件发生频率和严重程度较低,导致治疗中断较少,无死亡病例。4名患者在服用美拉胂醇-硝呋替莫时死亡,1名患者服用美拉胂醇-依氟鸟氨酸时死亡。结论:N+E组合似乎是一种很有希望的一线治疗方法,可以改善昏睡病的治疗,尽管这项中断的研究的结果不允许结论性的解释。需要进行更大规模的研究,以继续评估这种药物组合治疗布氏冈比亚锥虫昏睡病的效果。
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