A randomized, open-label clinical trial comparing the long-term effects of miltefosine and meglumine antimoniate for mucosal leishmaniasis
Rev. Soc. Bras. Med. Trop
; 52: e20180292, 2019. tab, graf
Article
em En
| LILACS
| ID: biblio-990435
Biblioteca responsável:
BR1.1
ABSTRACT
Abstract INTRODUCTION:
The treatment of mucosal leishmaniasis (ML) is difficult due to the toxicity and route of administration of standard drugs. Miltefosine is an oral agent used for leishmaniasis treatment; however, no data exist regarding its use for ML in Brazil. In this study, we aimed to evaluate the efficacy of miltefosine for ML treatment compared to that of pentavalent antimonial in a pilot study.METHODS:
We performed a randomized clinical trial with two parallel groups. The tested intervention consisted of miltefosine 1.3-2 mg/kg/day (two capsules) for 28 days or intravenous 20 mg SbV/kg/day of meglumine antimoniate (N-MA) for 30 days. The final endpoint was defined as complete healing of the lesion four years after treatment. We also analyzed an early endpoint at 90 days after treatment.RESULTS:
Forty patients were included in this study each experimental group comprised 20 patients. Applying a multivariate model in an intention-to-treat analysis, we observed that patients treated with miltefosine had a cure probability 2.08 times greater (95% confidence interval [CI] = 1.03-4.18) than those treated with N-MA at 90 days after treatment. At the final endpoint, we observed no differences in cure probability between miltefosine and N-MA (relative risk = 0.66; 95% CI = 0.33-1.32). With respect to adverse reactions, significant differences between groups were related to gastrointestinal effects, which were more frequent in the miltefosine group.CONCLUSIONS:
Miltefosine may be an interesting alternative for treating ML because of its oral administration and cure rate after long-term follow-up.Palavras-chave
Texto completo:
1
Base de dados:
LILACS
Assunto principal:
Fosforilcolina
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Leishmaniose Mucocutânea
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Antimoniato de Meglumina
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Antiprotozoários
Tipo de estudo:
Clinical_trials
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Etiology_studies
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Prognostic_studies
Limite:
Female
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Humans
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Male
Idioma:
En
Ano de publicação:
2019
Tipo de documento:
Article