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硝呋替莫-依氟鸟氨酸联合疗法治疗布氏冈比亚锥虫二期昏睡病:刚果的一项随机临床试验

Nifurtimox-eflornithine combination therapy for second-stage Trypanosoma brucei gambiense sleeping sickness: a randomized clinical trial in Congo.

作者信息

Priotto Gerardo, Kasparian Serena, Ngouama Daniel, Ghorashian Sara, Arnold Ute, Ghabri Salah, Karunakara Unni

机构信息

Epicentre, Paris, France.

出版信息

Clin Infect Dis. 2007 Dec 1;45(11):1435-42. doi: 10.1086/522982. Epub 2007 Oct 22.

Abstract

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.

摘要

背景

由布氏冈比亚锥虫引起的人类非洲锥虫病是一种致命疾病。目前针对二期疾病患者的治疗选择要么毒性极高,要么在野外条件下不实用。我们比较了硝呋莫司-依氟鸟氨酸联合用药与标准依氟鸟氨酸方案治疗二期疾病的疗效和安全性。

方法

在刚果共和国布恩泽省恩卡伊由无国界医生组织运营的昏睡病治疗中心进行了一项随机、开放标签、活性对照的III期临床试验,比较两个治疗组。对患者进行筛选以确定是否符合纳入标准,并随机分配接受单独的依氟鸟氨酸治疗(每天400mg/kg,每6小时静脉注射一次,共14天)或依氟鸟氨酸(每天400mg/kg,每12小时静脉注射一次,共7天)加硝呋莫司(每天15mg/kg,每8小时口服一次,共10天)。对患者进行18个月的观察。研究结果为治愈情况和治疗引起的不良事件。

结果

共招募了103例二期疾病患者。依氟鸟氨酸组的治愈率为94.1%,硝呋莫司-依氟鸟氨酸组为96.2%。两组药物反应均很常见,严重反应分别影响了依氟鸟氨酸组25.5%的患者和硝呋莫司-依氟鸟氨酸组9.6%的患者,分别导致2例和1例治疗中断。依氟鸟氨酸组有1例死亡,硝呋莫司-依氟鸟氨酸组无死亡病例。

结论

硝呋莫司-依氟鸟氨酸联合用药似乎是二期昏睡病有前景的一线治疗方法。如果我们的研究结果得到其他地点正在进行的研究结果(本研究的多中心扩展)的证实,新的硝呋莫司-依氟鸟氨酸联合疗法将标志着相对于当前疗法的重大且多方面的进步。

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