Tropical Medicine Centre, Infectious Diseases Department, Ramón y Cajal Hospital, Madrid, Spain.
Clin Infect Dis. 2015 May 1;60(9):1398-404. doi: 10.1093/cid/civ004. Epub 2015 Jan 18.
Miltefosine is the only recognized oral agent with potential to treat leishmaniasis. Miltefosine had demonstrated very good cure rates for visceral leishmaniasis (VL) in India, Nepal, and Bangladesh, but high rates of clinical failures have been recently reported. Moderate efficacy has been observed for VL in East Africa, whereas data from Mediterranean countries and Latin America are scarce. Results have not been very promising for patients coinfected with VL and human immunodeficiency virus. However, miltefosine's long half-life and its oral administration could make it a good option for maintenance prophylaxis. Good evidence of efficacy has been documented in Old World cutaneous leishmaniasis (CL), and different cure rates among New World CL have been obtained depending on the geographical areas and species involved. Appropriate regimens for New World mucocutaneous leishmaniasis need to be established, although longer treatment duration seems to confer better results. Strategies to prevent the development and spread of miltefosine resistance are urgently needed.
米替福新是唯一被认可的具有治疗内脏利什曼病(VL)潜力的口服药物。在印度、尼泊尔和孟加拉国,米替福新已被证明对内脏利什曼病(VL)有非常好的治愈率,但最近有报道称其临床失败率很高。在东非,米替福新对 VL 的疗效中等,而来自地中海国家和拉丁美洲的数据则很少。对于同时感染 VL 和人类免疫缺陷病毒(HIV)的患者,疗效并不十分理想。然而,米替福新的半衰期长且为口服制剂,这使其成为维持预防的一个不错的选择。在旧世界皮肤利什曼病(CL)中已经有了很好的疗效证据,而在新世界 CL 中,由于涉及的地理区域和物种不同,获得了不同的治愈率。需要建立针对新世界黏膜皮肤利什曼病的适当治疗方案,尽管较长的治疗时间似乎能带来更好的效果。迫切需要制定预防米替福新耐药性发展和传播的策略。