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New Frontiers in the Treatment of Multiple Myeloma

Recent leaps in elucidating the biology of myeloma, particularly the intracellular pathways and the complex interaction with the bone marrow microenvironment, have resulted in an unprecedented surge of novel, targeted therapies and therapeutic regimens. There are currently over 30 new agents being t...

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Detalles Bibliográficos
Autores principales: Hwang, Janice Jin, Ghobrial, Irene M., Anderson, Kenneth C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133623/
https://www.ncbi.nlm.nih.gov/pubmed/17160337
http://dx.doi.org/10.1100/tsw.2006.236
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author Hwang, Janice Jin
Ghobrial, Irene M.
Anderson, Kenneth C.
author_facet Hwang, Janice Jin
Ghobrial, Irene M.
Anderson, Kenneth C.
author_sort Hwang, Janice Jin
collection PubMed
description Recent leaps in elucidating the biology of myeloma, particularly the intracellular pathways and the complex interaction with the bone marrow microenvironment, have resulted in an unprecedented surge of novel, targeted therapies and therapeutic regimens. There are currently over 30 new agents being tested in the treatment of multiple myeloma (MM). Many of these are novel, targeted agents that have demonstrated significant efficacy and prolonged survival. In this review, we summarize the current understanding of the mechanisms of action of novel therapies being tested in the preclinical and clinical settings in MM. These include agents that act directly on the intracellular signaling pathways, cell maintenance processes, and cell surface receptors. Finally, we present the clinical responses to some of these agents when used alone or in combination in clinical trials of patients with MM. Indeed, MM has become a model disease for the development of novel, therapeutic agents.
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spelling pubmed-31336232011-07-12 New Frontiers in the Treatment of Multiple Myeloma Hwang, Janice Jin Ghobrial, Irene M. Anderson, Kenneth C. ScientificWorldJournal Review Article Recent leaps in elucidating the biology of myeloma, particularly the intracellular pathways and the complex interaction with the bone marrow microenvironment, have resulted in an unprecedented surge of novel, targeted therapies and therapeutic regimens. There are currently over 30 new agents being tested in the treatment of multiple myeloma (MM). Many of these are novel, targeted agents that have demonstrated significant efficacy and prolonged survival. In this review, we summarize the current understanding of the mechanisms of action of novel therapies being tested in the preclinical and clinical settings in MM. These include agents that act directly on the intracellular signaling pathways, cell maintenance processes, and cell surface receptors. Finally, we present the clinical responses to some of these agents when used alone or in combination in clinical trials of patients with MM. Indeed, MM has become a model disease for the development of novel, therapeutic agents. TheScientificWorldJOURNAL 2006-12-06 /pmc/articles/PMC3133623/ /pubmed/17160337 http://dx.doi.org/10.1100/tsw.2006.236 Text en Copyright © 2006 Janice Jin Hwang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hwang, Janice Jin
Ghobrial, Irene M.
Anderson, Kenneth C.
New Frontiers in the Treatment of Multiple Myeloma
title New Frontiers in the Treatment of Multiple Myeloma
title_full New Frontiers in the Treatment of Multiple Myeloma
title_fullStr New Frontiers in the Treatment of Multiple Myeloma
title_full_unstemmed New Frontiers in the Treatment of Multiple Myeloma
title_short New Frontiers in the Treatment of Multiple Myeloma
title_sort new frontiers in the treatment of multiple myeloma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133623/
https://www.ncbi.nlm.nih.gov/pubmed/17160337
http://dx.doi.org/10.1100/tsw.2006.236
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