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内脏利什曼病联合治疗的现状:更新综述。

The status of combination therapy for visceral leishmaniasis: an updated review.

机构信息

Institute of Tropical Medicine, Antwerp, Belgium.

Department of Pharmacy, Uppsala University, Uppsala, Sweden; Department of Pharmacy and Pharmacology, Netherlands Cancer Institute, Amsterdam, Netherlands.

出版信息

Lancet Infect Dis. 2024 Jan;24(1):e36-e46. doi: 10.1016/S1473-3099(23)00353-5. Epub 2023 Aug 25.

Abstract

For the past 15 years, trials of combination therapy options for visceral leishmaniasis have been conducted with the aim of identifying effective, and safe treatment regimens that were shorter than existing monotherapy regimens and could also prevent or delay the emergence of drug resistance. Although first-line treatment currently relies on combination therapy in east Africa, this is not true in Latin America owing to disappointing trial results, with lower than expected efficacy seen for the combination treatment group. By contrast, several effective combination therapy regimens have been identified through trials on the Indian subcontinent; yet, first-line therapy is still AmBisome monotherapy as the drug is part of a free donation programme and is highly effective in this region. Achieving a short all-oral combination treatment will require new chemical entities, several of which are currently under evaluation. Future studies should systematically include pharmacological substudies to ensure optimal dosing for all patient groups. To achieve maximal impact of new combination treatments, mechanisms to ensure drug availability and access after trials should be established. Enhancing the longevity of current and novel treatments will require effective systems for early detection of emerging drug resistance.

摘要

在过去的 15 年中,一直在进行内脏利什曼病联合治疗方案的试验,目的是确定比现有单一疗法更短、更有效且能预防或延迟耐药性出现的治疗方案。尽管在东非,一线治疗目前依赖联合疗法,但在拉丁美洲并非如此,因为试验结果令人失望,联合治疗组的疗效低于预期。相比之下,通过在印度次大陆进行的试验已经确定了几种有效的联合治疗方案;然而,一线治疗仍然是两性霉素 B 脂质体单药治疗,因为该药物是一项免费捐赠计划的一部分,在该地区非常有效。实现一种短期的全口服联合治疗方案将需要新的化学实体,目前正在对其中几种进行评估。未来的研究应系统地包括药理学子研究,以确保所有患者群体的最佳剂量。为了实现新的联合治疗方案的最大影响,应建立试验后确保药物供应和可及性的机制。为了延长现有和新型治疗方案的寿命,需要建立有效的系统来早期发现新出现的耐药性。

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