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单次服用他非诺喹预防间日疟原虫疟疾复发。

Single-Dose Tafenoquine to Prevent Relapse of Plasmodium vivax Malaria.

机构信息

From Fundação de Medicina Tropical Dr Heitor Vieira Dourado, Manaus (M.V.G.L., F.V., W.M.M., M.A.M.B., M.R.F.C.), Fundação Oswaldo Cruz, Manguinhos, Rio de Janeiro (M.V.G.L.), and Centro de Pesquisa em Medicina Tropical Rondônia, Porto Velho (D.B.P., M.S.T.) - all in Brazil; Universidad Peruana Cayetano Heredia, Lima, Peru (A.L.-C., R.C., M.C.); Mahidol University (S.K.) and the Armed Forces Research Institute of Medical Sciences (C.L., D.L.S., N.B.), Bangkok, Thailand; the University of Gondar, Gondar (R.M., E.D., S.G., K.M.W.), and Jimma University, Jimma (D.Y., A.A., A.Z., C.A.) - both in Ethiopia; Research Institute for Tropical Medicine, Manila (F.E.J.E.), and Rio Tuba Nickel Foundation Hospital, Palawan (R.Z.M.) - both in the Philippines; Medical University of Vienna, Vienna (H.N.); Swiss Tropical and Public Health Institute and University of Basel, Basel (F.B., H.-P.B.), and Medicines for Malaria Venture, Geneva (S.D.) - both in Switzerland; Oxford University, Oxford (B.A.), and GlaxoSmithKline, Stockley Park West (J.-P.K., L.M.K., V.M.R., S.W.J., E.H., K.M., D.D.C., K.F., C.O.U., J.A.G., G.C.K.W.K.) - both in the United Kingdom; and GlaxoSmithKline, Collegeville, PA (J.J.B.).

出版信息

N Engl J Med. 2019 Jan 17;380(3):215-228. doi: 10.1056/NEJMoa1710775.

Abstract

BACKGROUND

Treatment of Plasmodium vivax malaria requires the clearing of asexual parasites, but relapse can be prevented only if dormant hypnozoites are cleared from the liver (a treatment termed "radical cure"). Tafenoquine is a single-dose 8-aminoquinoline that has recently been registered for the radical cure of P. vivax.

METHODS

This multicenter, double-blind, double-dummy, parallel group, randomized, placebo-controlled trial was conducted in Ethiopia, Peru, Brazil, Cambodia, Thailand, and the Philippines. We enrolled 522 patients with microscopically confirmed P. vivax infection (>100 to <100,000 parasites per microliter) and normal glucose-6-phosphate dehydrogenase (G6PD) activity (with normal activity defined as ≥70% of the median value determined at each trial site among 36 healthy male volunteers who were otherwise not involved in the trial). All patients received a 3-day course of chloroquine (total dose of 1500 mg). In addition, patients were assigned to receive a single 300-mg dose of tafenoquine on day 1 or 2 (260 patients), placebo (133 patients), or a 15-mg dose of primaquine once daily for 14 days (129 patients). The primary outcome was the Kaplan-Meier estimated percentage of patients who were free from recurrence at 6 months, defined as P. vivax clearance without recurrent parasitemia.

RESULTS

In the intention-to-treat population, the percentage of patients who were free from recurrence at 6 months was 62.4% in the tafenoquine group (95% confidence interval [CI], 54.9 to 69.0), 27.7% in the placebo group (95% CI, 19.6 to 36.6), and 69.6% in the primaquine group (95% CI, 60.2 to 77.1). The hazard ratio for the risk of recurrence was 0.30 (95% CI, 0.22 to 0.40) with tafenoquine as compared with placebo (P<0.001) and 0.26 (95% CI, 0.18 to 0.39) with primaquine as compared with placebo (P<0.001). Tafenoquine was associated with asymptomatic declines in hemoglobin levels, which resolved without intervention.

CONCLUSIONS

Single-dose tafenoquine resulted in a significantly lower risk of P. vivax recurrence than placebo in patients with phenotypically normal G6PD activity. (Funded by GlaxoSmithKline and Medicines for Malaria Venture; DETECTIVE ClinicalTrials.gov number, NCT01376167 .).

摘要

背景

治疗间日疟原虫疟疾需要清除无性体寄生虫,但只有清除肝脏中的休眠原虫(称为“根治性治疗”)才能预防复发。他非诺喹是一种单剂量 8-氨基喹啉,最近已注册用于根治间日疟原虫。

方法

这项多中心、双盲、双模拟、平行组、随机、安慰剂对照试验在埃塞俄比亚、秘鲁、巴西、柬埔寨、泰国和菲律宾进行。我们招募了 522 名显微镜证实的间日疟原虫感染(每微升>100 至<100,000 个寄生虫)且葡萄糖-6-磷酸脱氢酶(G6PD)活性正常的患者(正常活性定义为在每个试验地点的 36 名健康男性志愿者中确定的中位数的 70%以上,这些志愿者未参与试验)。所有患者均接受 3 天氯喹治疗(总剂量 1500mg)。此外,患者被分配在第 1 天或第 2 天接受单次 300mg 他非诺喹(260 名患者)、安慰剂(133 名患者)或每日 15mg 伯氨喹治疗 14 天(129 名患者)。主要结局是 Kaplan-Meier 估计的 6 个月无复发患者比例,定义为无复发寄生虫血症的间日疟原虫清除。

结果

在意向治疗人群中,他非诺喹组 6 个月无复发患者的比例为 62.4%(95%置信区间[CI],54.9 至 69.0),安慰剂组为 27.7%(95%CI,19.6 至 36.6),伯氨喹组为 69.6%(95%CI,60.2 至 77.1)。与安慰剂相比,他非诺喹组的复发风险比为 0.30(95%CI,0.22 至 0.40)(P<0.001),与安慰剂相比,伯氨喹组的复发风险比为 0.26(95%CI,0.18 至 0.39)(P<0.001)。他非诺喹与血红蛋白水平无症状下降有关,无需干预即可自行恢复。

结论

在表型正常 G6PD 活性的患者中,单次剂量他非诺喹与安慰剂相比,降低间日疟复发的风险显著降低。(由葛兰素史克和疟疾药物开发伙伴关系资助;临床试验编号:DETECTIVE,NCT01376167)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92bf/6657226/43ba2516d58b/NEJM-2019-1710775-g001.jpg

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