Cargando…
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...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1782252553133621248 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3518293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Informa UK, Ltd. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT balasegarammanica liposomalamphotericinbasatreatmentforhumanleishmaniasis AT ritmeijerkoert liposomalamphotericinbasatreatmentforhumanleishmaniasis AT limamariaangeles liposomalamphotericinbasatreatmentforhumanleishmaniasis AT burzasakib liposomalamphotericinbasatreatmentforhumanleishmaniasis AT ortizgenovesegemma liposomalamphotericinbasatreatmentforhumanleishmaniasis AT milanibarbara liposomalamphotericinbasatreatmentforhumanleishmaniasis AT gaspanisara liposomalamphotericinbasatreatmentforhumanleishmaniasis AT potetjulien liposomalamphotericinbasatreatmentforhumanleishmaniasis AT chappuisfrancois liposomalamphotericinbasatreatmentforhumanleishmaniasis |