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Eribulin in Cancer Treatment

Halichondrin B is a complex, natural, polyether macrolide derived from marine sponges. Eribulin is a structurally-simplified, synthetic, macrocyclic ketone analogue of Halichondrin B. Eribulin was approved by United States Food and Drug Administration in 2010 as a third-line therapy for metastatic b...

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Detalles Bibliográficos
Autores principales: Swami, Umang, Shah, Umang, Goel, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557013/
https://www.ncbi.nlm.nih.gov/pubmed/26262627
http://dx.doi.org/10.3390/md13085016
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author Swami, Umang
Shah, Umang
Goel, Sanjay
author_facet Swami, Umang
Shah, Umang
Goel, Sanjay
author_sort Swami, Umang
collection PubMed
description Halichondrin B is a complex, natural, polyether macrolide derived from marine sponges. Eribulin is a structurally-simplified, synthetic, macrocyclic ketone analogue of Halichondrin B. Eribulin was approved by United States Food and Drug Administration in 2010 as a third-line therapy for metastatic breast cancer patients who have previously been treated with an anthracycline and a taxane. It has a unique microtubule dynamics inhibitory action. Phase III studies have either been completed or are currently ongoing in breast cancer, soft tissue sarcoma, and non-small cell lung cancer. Phase I and II studies in multiple cancers and various combinations are currently ongoing. This article reviews the available information on eribulin with respect to its clinical pharmacology, pharmacokinetics, pharmacodynamics, mechanism of action, metabolism, preclinical studies, and with special focus on clinical trials.
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spelling pubmed-45570132015-09-03 Eribulin in Cancer Treatment Swami, Umang Shah, Umang Goel, Sanjay Mar Drugs Review Halichondrin B is a complex, natural, polyether macrolide derived from marine sponges. Eribulin is a structurally-simplified, synthetic, macrocyclic ketone analogue of Halichondrin B. Eribulin was approved by United States Food and Drug Administration in 2010 as a third-line therapy for metastatic breast cancer patients who have previously been treated with an anthracycline and a taxane. It has a unique microtubule dynamics inhibitory action. Phase III studies have either been completed or are currently ongoing in breast cancer, soft tissue sarcoma, and non-small cell lung cancer. Phase I and II studies in multiple cancers and various combinations are currently ongoing. This article reviews the available information on eribulin with respect to its clinical pharmacology, pharmacokinetics, pharmacodynamics, mechanism of action, metabolism, preclinical studies, and with special focus on clinical trials. MDPI 2015-08-07 /pmc/articles/PMC4557013/ /pubmed/26262627 http://dx.doi.org/10.3390/md13085016 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Swami, Umang
Shah, Umang
Goel, Sanjay
Eribulin in Cancer Treatment
title Eribulin in Cancer Treatment
title_full Eribulin in Cancer Treatment
title_fullStr Eribulin in Cancer Treatment
title_full_unstemmed Eribulin in Cancer Treatment
title_short Eribulin in Cancer Treatment
title_sort eribulin in cancer treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557013/
https://www.ncbi.nlm.nih.gov/pubmed/26262627
http://dx.doi.org/10.3390/md13085016
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