Abstract

BackgroundComplex cutaneous and muco-cutaneous leishmaniasis (CL and MCL) often requires systemic therapy. Liposomal amphotericin B (L-AmB) has a strong potential for a solid clinical benefit in this indication.MethodsWe conducted a retrospective analysis of data from a French centralized referral treatment program and from the “LeishMan” European consortium database. All patients with parasitologically proven CL or MCL who received at least one dose of L-AmB were included. Positive outcome was based on ulcer closure as per recent WHO workshop guidelines.ResultsFrom 2008 through 2016, 43 travelers returning from 18 countries (Old World n = 28; New World n = 15) were analyzed with a median follow-up duration of 79 days [range 28–803]. Main clinical forms were: localized CL with one or multiple lesions (n = 32; 74%) and MCL (n = 8; 19%). As per published criteria 19 of 41 patients (46%) were cured 90 days after one course of L-AmB. When the following items -improvement before day 90 but no subsequent follow-up, delayed healing (>3 months) and healing after a second course of L-AmB- were included in the definition of cure, 27 of 43 patients (63%) had a positive outcome. Five patients (MCL = 1; CL = 4) experienced a relapse after a median duration of 6 months [range 3–27] post treatment and 53% of patients (23/43) experienced at least one adverse event including severe hypokalaemia and acute cardiac failure (one patient each). In multivariate analysis, tegumentary infection with L. infantum was associated with complete healing after L-AmB therapy (OR 5.8 IC 95% [1.03–32]) while infection with other species had no impact on outcome.ConclusionIn conditions close to current medical practice, the therapeutic window of L-AmB was narrow in travellers with CL or MCL, with the possible exception of those infected with L. infantum. Strict follow-up is warranted when using L-AmB in patients with mild disease.

Highlights

  • Tegumentary leishmaniasis (TL) occurs when one of the 20 Leishmania species that can infect humans causes lesions of the skin or mucosae

  • Tegumentary infection with L. infantum was associated with complete healing after liposomal amphotericin B (L-AmB) therapy while infection with other species had no impact on outcome

  • In conditions close to current medical practice, the therapeutic window of L-AmB was narrow in travellers with CL or MCL, with the possible exception of those infected with L. infantum

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Summary

Introduction

Tegumentary leishmaniasis (TL) occurs when one of the 20 Leishmania species that can infect humans causes lesions of the skin or mucosae. Because TL is observed in patients of all ages, Liposomal amphotericin B in cutaneous and muco-cutaneous leishmaniasis either immunocompetent or immunocompromised, the result is a wide continuum of clinical forms and medical situations for which a multiplicity of treatment approaches have been proposed. Despite the high global burden of cutaneous and muco-cutaneous leishmaniasis (CL and MCL) and the rising number of travels to endemic areas, there is still relatively sparse evidence to support an accurate choice between local (e.g. cryotherapy and/or intralesional antimony, topical paromomycin) or systemic therapy (e.g. amphotericin B, miltefosine, pentavalent antimonials, pentamidine, fluconazole). Among the currently available systemic antileishmanial agents, liposomal amphotericin B (L-AmB) has a strong potential for a high clinical benefit in TL. Cure rates around 90% were reported in the treatment of MCL with deoxycholate amphotericin B or with liposomal forms [10]. Liposomal amphotericin B (L-AmB) has a strong potential for a solid clinical benefit in this indication

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