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Liposomal amphotericin B as a treatment for human leishmaniasis

INTRODUCTION: Leishmaniasis is a parasitic disease transmitted by phlebotomine sandflies. Between 700,000 and 1.2 million cases of cutaneous leishmaniasis and between 200,000 and 400,000 cases of visceral leishmaniasis (VL), which is fatal if left untreated, occur annually worldwide. Liposomal ampho...

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Autores principales: Balasegaram, Manica, Ritmeijer, Koert, Lima, Maria Angeles, Burza, Sakib, Ortiz Genovese, Gemma, Milani, Barbara, Gaspani, Sara, Potet, Julien, Chappuis, François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa UK, Ltd. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518293/
https://www.ncbi.nlm.nih.gov/pubmed/23167833
http://dx.doi.org/10.1517/14728214.2012.748036
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author Balasegaram, Manica
Ritmeijer, Koert
Lima, Maria Angeles
Burza, Sakib
Ortiz Genovese, Gemma
Milani, Barbara
Gaspani, Sara
Potet, Julien
Chappuis, François
author_facet Balasegaram, Manica
Ritmeijer, Koert
Lima, Maria Angeles
Burza, Sakib
Ortiz Genovese, Gemma
Milani, Barbara
Gaspani, Sara
Potet, Julien
Chappuis, François
author_sort Balasegaram, Manica
collection PubMed
description INTRODUCTION: Leishmaniasis is a parasitic disease transmitted by phlebotomine sandflies. Between 700,000 and 1.2 million cases of cutaneous leishmaniasis and between 200,000 and 400,000 cases of visceral leishmaniasis (VL), which is fatal if left untreated, occur annually worldwide. Liposomal amphotericin B (LAMB), alone or in combination with other drugs, has been extensively studied as VL treatment, but data on routine field use are limited, and several challenges to patients' access to this life-saving drug remain. AREAS COVERED: This article provides a review of clinical studies on LAMB for VL and other forms of leishmaniasis. The current development of generic versions of LAMB and related challenges are also discussed. EXPERT OPINION: LAMB proved to be highly efficacious and safe in over 8000 VL patients treated by MÉdecins Sans Frontières in South Asia, and its use was feasible even at primary healthcare level. Despite requiring higher doses, LAMB is the drug of choice to treat vulnerable groups (e.g., pregnant or HIV positive) and relapsing VL patients in East Africa. LAMB should be included in national VL guidelines and registered in all VL endemic countries. Its cost should be further reduced and regulatory pathways to prove bioequivalence for generic LAMB products should be implemented.
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spelling pubmed-35182932012-12-12 Liposomal amphotericin B as a treatment for human leishmaniasis Balasegaram, Manica Ritmeijer, Koert Lima, Maria Angeles Burza, Sakib Ortiz Genovese, Gemma Milani, Barbara Gaspani, Sara Potet, Julien Chappuis, François Expert Opin Emerg Drugs Reviews INTRODUCTION: Leishmaniasis is a parasitic disease transmitted by phlebotomine sandflies. Between 700,000 and 1.2 million cases of cutaneous leishmaniasis and between 200,000 and 400,000 cases of visceral leishmaniasis (VL), which is fatal if left untreated, occur annually worldwide. Liposomal amphotericin B (LAMB), alone or in combination with other drugs, has been extensively studied as VL treatment, but data on routine field use are limited, and several challenges to patients' access to this life-saving drug remain. AREAS COVERED: This article provides a review of clinical studies on LAMB for VL and other forms of leishmaniasis. The current development of generic versions of LAMB and related challenges are also discussed. EXPERT OPINION: LAMB proved to be highly efficacious and safe in over 8000 VL patients treated by MÉdecins Sans Frontières in South Asia, and its use was feasible even at primary healthcare level. Despite requiring higher doses, LAMB is the drug of choice to treat vulnerable groups (e.g., pregnant or HIV positive) and relapsing VL patients in East Africa. LAMB should be included in national VL guidelines and registered in all VL endemic countries. Its cost should be further reduced and regulatory pathways to prove bioequivalence for generic LAMB products should be implemented. Informa UK, Ltd. 2012-12 2012-11-20 /pmc/articles/PMC3518293/ /pubmed/23167833 http://dx.doi.org/10.1517/14728214.2012.748036 Text en © Informa UK, Ltd. http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited.
spellingShingle Reviews
Balasegaram, Manica
Ritmeijer, Koert
Lima, Maria Angeles
Burza, Sakib
Ortiz Genovese, Gemma
Milani, Barbara
Gaspani, Sara
Potet, Julien
Chappuis, François
Liposomal amphotericin B as a treatment for human leishmaniasis
title Liposomal amphotericin B as a treatment for human leishmaniasis
title_full Liposomal amphotericin B as a treatment for human leishmaniasis
title_fullStr Liposomal amphotericin B as a treatment for human leishmaniasis
title_full_unstemmed Liposomal amphotericin B as a treatment for human leishmaniasis
title_short Liposomal amphotericin B as a treatment for human leishmaniasis
title_sort liposomal amphotericin b as a treatment for human leishmaniasis
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3518293/
https://www.ncbi.nlm.nih.gov/pubmed/23167833
http://dx.doi.org/10.1517/14728214.2012.748036
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