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Clinical trials with anti-angiogenic agents in hematological malignancies

New blood vessel formation (angiogenesis) is not only essential for the growth of solid tumors but there is also emerging evidence that progression of hematological malignancies like multiple myeloma, acute leukemias, and myeloproliferative neoplasms, also depends on new blood vessel formation. Anti...

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Detalles Bibliográficos
Autores principales: Medinger, Michael, Mross, Klaus
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902424/
https://www.ncbi.nlm.nih.gov/pubmed/20569499
http://dx.doi.org/10.1186/2040-2384-2-10
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author Medinger, Michael
Mross, Klaus
author_facet Medinger, Michael
Mross, Klaus
author_sort Medinger, Michael
collection PubMed
description New blood vessel formation (angiogenesis) is not only essential for the growth of solid tumors but there is also emerging evidence that progression of hematological malignancies like multiple myeloma, acute leukemias, and myeloproliferative neoplasms, also depends on new blood vessel formation. Anti-angiogenic strategies have become an important therapeutic modality for solid tumors. Several anti-angiogenic agents targeting angiogenesis-related pathways like monoclonal antibodies, receptor tyrosine kinase inhibitors, immunomodulatory drugs, and proteasome inhibitors have been entered clinical trials or have been already approved for the treatment of hematological malignancies as well and in some instances these pathways have emerged as promising therapeutic targets. This review summarizes recent advances in the basic understanding of the role of angiogenesis in hematological malignancies and clinical trials with novel therapeutic approaches targeting angiogenesis.
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spelling pubmed-29024242010-07-13 Clinical trials with anti-angiogenic agents in hematological malignancies Medinger, Michael Mross, Klaus J Angiogenes Res Review New blood vessel formation (angiogenesis) is not only essential for the growth of solid tumors but there is also emerging evidence that progression of hematological malignancies like multiple myeloma, acute leukemias, and myeloproliferative neoplasms, also depends on new blood vessel formation. Anti-angiogenic strategies have become an important therapeutic modality for solid tumors. Several anti-angiogenic agents targeting angiogenesis-related pathways like monoclonal antibodies, receptor tyrosine kinase inhibitors, immunomodulatory drugs, and proteasome inhibitors have been entered clinical trials or have been already approved for the treatment of hematological malignancies as well and in some instances these pathways have emerged as promising therapeutic targets. This review summarizes recent advances in the basic understanding of the role of angiogenesis in hematological malignancies and clinical trials with novel therapeutic approaches targeting angiogenesis. BioMed Central 2010-06-22 /pmc/articles/PMC2902424/ /pubmed/20569499 http://dx.doi.org/10.1186/2040-2384-2-10 Text en Copyright ©2010 Medinger and Mross; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Medinger, Michael
Mross, Klaus
Clinical trials with anti-angiogenic agents in hematological malignancies
title Clinical trials with anti-angiogenic agents in hematological malignancies
title_full Clinical trials with anti-angiogenic agents in hematological malignancies
title_fullStr Clinical trials with anti-angiogenic agents in hematological malignancies
title_full_unstemmed Clinical trials with anti-angiogenic agents in hematological malignancies
title_short Clinical trials with anti-angiogenic agents in hematological malignancies
title_sort clinical trials with anti-angiogenic agents in hematological malignancies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902424/
https://www.ncbi.nlm.nih.gov/pubmed/20569499
http://dx.doi.org/10.1186/2040-2384-2-10
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