Medicines for Malaria Venture, Route de Pré-Bois 20, 1215, Geneva 15, Switzerland.
Bill and Melinda Gates Foundation, Seattle, USA.
Malar J. 2020 Mar 14;19(1):111. doi: 10.1186/s12936-020-03184-x.
Tafenoquine is an 8-aminoquinoline anti-malarial drug recently approved as a single-dose (300 mg) therapy for Plasmodium vivax relapse prevention, when co-administered with 3-days of chloroquine or other blood schizonticide. Tafenoquine 200 mg weekly after a loading dose is also approved as travellers' prophylaxis. The development of tafenoquine has been conducted over many years, using various dosing regimens in diverse populations.
This review brings together all the preclinical and clinical data concerning tafenoquine central nervous system safety. Data were assembled from published sources. The risk of neuropsychiatric adverse events (NPAEs) with single-dose tafenoquine (300 mg) in combination with chloroquine to achieve P. vivax relapse prevention is particularly examined.
There was no evidence of neurotoxicity with tafenoquine in preclinical animal models. In clinical studies in P. vivax relapse prevention, nervous system adverse events, mainly headache and dizziness, occurred in 11.4% (36/317) of patients with tafenoquine (300 mg)/chloroquine versus 10.2% (19/187) with placebo/chloroquine; and in 15.5% (75/483) of patients with tafenoquine/chloroquine versus 13.3% (35/264) with primaquine (15 mg/day for 14 days)/chloroquine. Psychiatric adverse events, mainly insomnia, occurred in 3.8% (12/317) of patients with tafenoquine/chloroquine versus 2.7% (5/187) with placebo/chloroquine; and in 2.9% (14/483) of patients with tafenoquine/chloroquine versus 3.4% (9/264) for primaquine/chloroquine. There were no serious or severe NPAEs observed with tafenoquine (300 mg)/chloroquine in these studies.
The risk:benefit of single-dose tafenoquine/chloroquine in P. vivax relapse prevention is favourable in the presence of malaria, with a low risk of NPAEs, similar to that seen with chloroquine alone or primaquine/chloroquine.
他非喹啉是一种 8-氨基喹啉抗疟药物,最近被批准与氯喹或其他血裂殖体药物联合使用 3 天,作为预防间日疟原虫复发的单次剂量(300mg)疗法。每周给予负荷剂量 200mg 的他非喹啉也被批准用于旅行者预防。他非喹啉的开发已经进行了多年,在不同人群中使用了各种剂量方案。
本综述汇集了所有关于他非喹啉中枢神经系统安全性的临床前和临床数据。数据来自已发表的资料。特别检查了单剂量他非喹啉(300mg)联合氯喹预防间日疟原虫复发的神经精神不良事件(NPAEs)的风险。
在临床前动物模型中,他非喹啉没有神经毒性的证据。在预防间日疟原虫复发的临床研究中,用他非喹啉(300mg)/氯喹治疗的患者中,神经系统不良事件(主要是头痛和头晕)发生率为 11.4%(36/317),而用安慰剂/氯喹治疗的患者中为 10.2%(19/187);用他非喹啉/氯喹治疗的患者中为 15.5%(75/483),而用 15mg/天,连用 14 天的伯氨喹/氯喹治疗的患者中为 13.3%(35/264)。用他非喹啉/氯喹治疗的患者中,精神不良事件(主要是失眠)发生率为 3.8%(12/317),而用安慰剂/氯喹治疗的患者中为 2.7%(5/187);用他非喹啉/氯喹治疗的患者中为 2.9%(14/483),而用伯氨喹/氯喹治疗的患者中为 3.4%(9/264)。在这些研究中,没有观察到用他非喹啉(300mg)/氯喹治疗时出现严重或严重的 NPAEs。
在存在疟疾的情况下,用单剂量他非喹啉/氯喹预防间日疟原虫复发的风险:效益是有利的,NPAEs 的风险低,与单独使用氯喹或伯氨喹/氯喹相似。