At a glance
- Leishmaniasis treatment depends on a variety of factors, and healthcare providers should consider safety precautions of different medications in different populations.
Treatment options
Note: The information provided here does not constitute a primer on treating leishmaniasis; rather, the focus is on basic principles and perspective, geared towards clinicians treating patients in the United States. Treatment decisions should be individualized, with expert consultation. In general, all clinically manifest cases of visceral leishmaniasis and mucosal leishmaniasis should be treated, whereas not all cases of cutaneous leishmaniasis (CL) require treatment.
The treatment approach depends in part on host and parasite factors. Some approaches/regimens are effective only against certain Leishmania species/strains and only from particular geographic regions. Even data from well-conducted clinical trials are not necessarily generalizable to other settings. Of particular note, data from the many clinical trials of therapy for VL in parts of India are not necessarily directly applicable to VL caused by L. donovani in other areas, to VL caused by other species, or to treatment of CL and ML.
Special groups (e.g., young children, elderly persons, pregnant/lactating women, and persons who are immunocompromised or who have other comorbidities) may need different medications or dosage regimens.
The relative merits of various treatment approaches/regimens can be discussed with CDC staff. In addition, in the United States, special considerations apply regarding the availability of particular medications to treat leishmaniasis:
- One parenteral agent, liposomal amphotericin B (AmBisome®), which is administered by IV infusion, is FDA-approved for treatment of VL (the approved indications do not include CL or ML).
- In 2014, FDA approved the oral agent miltefosine for treatment of CL, ML, and VL caused by particular Leishmania species (see below for details), in adults and adolescents at least 12 years of age who weigh at least 30 kg (66 pounds).
- Some medications that might have merit for treating selected cases of leishmaniasis are commercially available in the United States but the FDA-approved indications do not include leishmaniasis. Examples of such medications include the parenteral agents amphotericin B deoxycholate and pentamidine isethionate, as well as the orally administered "azoles" (ketoconazole, and fluconazole).
- Other medications that might have merit for treating selected cases of leishmaniasis currently are not available in the United States (such as the parenteral formulation of the aminoglycoside paromomycin) or are potentially available only through special mechanisms. For example, particular topical formations of paromomycin may be available through compounding pharmacies.
- Pentavalent antimonial (SbV) compounds, including sodium stibogluconate (Pentostam®) and meglumine antimoniate (Glucantime), are the traditional mainstays for treating leishmaniasis since the 1940s. They have not been approved by the Food and Drug Administration (FDA) and are not commercially available in the United States. Glucantime is available in the United States only under an individual investigational new drug protocol through the FDA. Sodium stibogluconate maybe be available in some countries outside of the US.
Cutaneous Leishmaniasis (CL)
Decisions about whether and how to treat should be individualized. The treatment approach depends in part on the Leishmania species/strain and the geographic area in which infection was acquired; the natural history of infection, the risk for mucosal dissemination/disease, the parasite's drug susceptibilities in the pertinent setting; and the number, size, location, evolution, and other clinical characteristics of the patient's skin lesions.
Treatment of CL may be indicated to:
- Decrease the risk for mucosal dissemination/disease (particularly for Western Hemisphere species in the Viannia subgenus);
- Accelerate the healing of the skin lesions;
- Decrease the risk for relapse (clinical reactivation) of the skin lesions;
- Decrease the local morbidity caused by large or persistent skin lesions, particularly those on the face or ears or near joints; and/or
- Decrease the reservoir of infection in geographic areas where infected persons (instead if other mammals) serve as reservoir hosts (such as in Kabul, Afghanistan, and other Leishmania tropica-endemic areas, where transmission is anthroponotic).
In general, the first sign of a therapeutic response to adequate treatment is decreasing induration (lesion flattening). The healing process for large, ulcerative lesions often continues after the end of therapy. Relapse (clinical reactivation) typically is noticed first at the margin of the lesion.
Conventional amphotericin B deoxycholate traditionally has been used as rescue therapy for CL and ML. Lipid formulations of amphotericin B typically are better tolerated than conventional amphotericin B. However, the data supporting their use for treatment of CL and ML are from case reports/series rather than from controlled clinical trials; standard dosage regimens have not been established. When liposomal amphotericin B has been used for treatment of CL, patients typically have received 3 mg per kg daily, by IV infusion, for a total of 6 to 10 or more doses.
In the United States, pentamidine isethionate is uncommonly used for treatment of CL. Its limitations include the potential for irreversible toxicity and variable effectiveness.
For pentavalent antimonial (SbV) therapy, including meglumine antimoniate (Glucantime) the standard daily dose is 20 mg of SbV per kg, administered IV or IM. The traditional duration of therapy is 20 days for CL (10 days may suffice in some settings) and 28 days for ML and VL. For some patients, adjustment of the daily dose or the duration of therapy may be indicated.
In 2014, FDA approved the oral agent miltefosine for treatment of CL in adults and adolescents who are not pregnant or breastfeeding. The FDA-approved indications are limited to infection caused by three particular species, all three of which are Western Hemisphere species in the Viannia subgenus—namely, Leishmania (V.) braziliensis, L. (V.) panamensis, and L. (V.) guyanensis. Even for these species, the effectiveness of miltefosine therapy has been variable in different geographic regions. Use of miltefosine for treatment of infection caused by other Leishmania species in the Western Hemisphere or by any species in the Eastern Hemisphere would constitute off-label use, as would treatment of children less than 12 years of age. See above for additional perspective and considerations regarding miltefosine.
- The FDA-approved treatment regimen for persons who weigh from 30 to 44 kg is as follows: one 50-mg oral capsule of miltefosine twice a day (total of 100 mg per day) for 28 consecutive days. The FDA-approved regimen for persons who weigh at least 45 kg (99 pounds) is one 50-mg capsule three times a day (total of 150 mg per day) for 28 consecutive days. Miltefosine is contraindicated in pregnant women. Women of reproductive potential should have a negative pregnancy test before starting therapy; they should be advised to use effective contraception during the treatment course and for 5 months thereafter. Nursing mothers should be advised not to breastfeed during the treatment course and for 5 months thereafter.
The "azoles" ketoconazole, itraconazole, and fluconazole—administered orally—have been used with mixed results, in various settings. For example:
- Ketoconazole (adult regimen: 600 mg daily for 28 days) showed modest activity against L. mexicana and L. (V.) panamensis infection in small studies in Guatemala and Panama, respectively.
- Itraconazole (adult regimen: 200 mg twice daily for 28 days) was ineffective against L. (V.) panamensis infection in a clinical trial in Colombia.
- Use of fluconazole (adult regimen: 200 mg daily for 6 weeks) for treatment of L. major infection in various countries in the Eastern Hemisphere has been associated with mixed results. Preliminary data from Iran suggested that a higher daily dose (400 vs. 200 mg) might be more effective against L. major infection. In northeastern Brazil, a low response rate to treatment with fluconazole (6.5–8.0 mg per kg per day for 28 days) was noted among adults infected with L. (V.) braziliensis.
Local Therapy
Some cases of CL might be candidates for local therapy, in part depending on the risk, if any, for mucosal dissemination/disease and on the number, location, size, and other characteristics of the skin lesions. Examples of local therapies that might have utility in some settings include cryotherapy (with liquid nitrogen), thermotherapy (use of localized current field radiofrequency heat), topical application of particular formulations of paromomycin, and intralesional (IL) administration of SbV. No standard IL treatment regimen has been established; various regimens have been used depending in part on the size and characteristics of the lesions.
The use of highly effective systemic therapy for VL is important, as is supportive care—for example, therapy for malnutrition, anemia/bleeding, and intercurrent infections. For HIV-coinfected patients, antiretroviral therapy (ART) should be started or optimized according to standard practice; appropriate use of ART may delay relapses and improve survival.
Liposomal amphotericin B is FDA-approved for treatment of VL and generally is the treatment of choice for U.S. patients. Although various regimens have been suggested in the published literature, the FDA-approved regimen for immunocompetent patients consists of 3 mg per kg daily, by IV infusion, on days 1–5, 14, and 21 (total dose of 21 mg/kg). The FDA-approved regimen for immunosuppressed patients consists of 4 mg per kg daily on days 1–5, 10, 17, 24, 31, and 38 (total dose of 40 mg/kg). Some immunosuppressed patients, including HIV-coinfected patients with CD4 counts <200 cells/mm3, may need even higher total doses and/or secondary prophylaxis (chronic maintenance therapy). However, standard approaches to antileishmanial treatment and secondary prophylaxis have not been established—for example, the optimal agent, dose, and dosing interval for maintenance therapy are unknown. Conventional amphotericin B deoxycholate is highly effective therapy for VL but generally is more toxic than liposomal amphotericin B.
In 2014, FDA approved the oral agent miltefosine for treatment of VL caused by Leishmania donovani, in adults and adolescents who are not pregnant or breastfeeding. Use of miltefosine for VL caused by other species (e.g., L. infantum) would constitute off-label use, as would treatment of children less than 12 years of age or weighing less than 30kg. See above for additional perspective and considerations regarding miltefosine.
Pentavalent antimonial (SbV) therapy generally remains highly effective therapy for VL in most geographic regions, with the notable exception of parts of South Asia. The standard dosage regimen for immunocompetent patients consists of 20 mg of SbV per kg daily, IV or IM, for 28 days. For some patients, adjustment of the daily dose or the duration of therapy may be indicated.
Other parenteral agents that have merit in some settings include paromomycin sulfate (the chemical equivalent of aminosidine), which is not available for parenteral administration in the United States—and—pentamidine isethionate, a second-line agent whose limitations include suboptimal effectiveness (most notably in parts of South Asia) and the potential for irreversible toxicity.