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New therapies for recurrent glioblastomas
Glioblastomas are the most common and deadliest form of malignant primary brain tumor. Until recently, therapies for tumors that recur after standard treatment have been largely ineffective. Recent phase II studies with the humanized monoclonal antibody against vascular endothelial growth factor bev...
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Formato: | Texto |
Lenguaje: | English |
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Medicine Reports
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948331/ https://www.ncbi.nlm.nih.gov/pubmed/20948683 http://dx.doi.org/10.3410/M1-94 |
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author | Wen, Patrick Y |
author_facet | Wen, Patrick Y |
author_sort | Wen, Patrick Y |
collection | PubMed |
description | Glioblastomas are the most common and deadliest form of malignant primary brain tumor. Until recently, therapies for tumors that recur after standard treatment have been largely ineffective. Recent phase II studies with the humanized monoclonal antibody against vascular endothelial growth factor bevacizumab suggest that this agent is active in recurrent glioblastomas, producing response rates of 26-40% and prolonging 6-month progression-free survival to 36-50%. As a result of these studies, the US Food and Drug Administration recently granted accelerated approval for bevacizumab as a treatment for recurrent glioblastomas. |
format | Text |
id | pubmed-2948331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Medicine Reports |
record_format | MEDLINE/PubMed |
spelling | pubmed-29483312010-10-14 New therapies for recurrent glioblastomas Wen, Patrick Y F1000 Med Rep Review Article Glioblastomas are the most common and deadliest form of malignant primary brain tumor. Until recently, therapies for tumors that recur after standard treatment have been largely ineffective. Recent phase II studies with the humanized monoclonal antibody against vascular endothelial growth factor bevacizumab suggest that this agent is active in recurrent glioblastomas, producing response rates of 26-40% and prolonging 6-month progression-free survival to 36-50%. As a result of these studies, the US Food and Drug Administration recently granted accelerated approval for bevacizumab as a treatment for recurrent glioblastomas. Medicine Reports 2009-12-09 /pmc/articles/PMC2948331/ /pubmed/20948683 http://dx.doi.org/10.3410/M1-94 Text en © 2009 Medicine Reports Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use this work for commercial purposes |
spellingShingle | Review Article Wen, Patrick Y New therapies for recurrent glioblastomas |
title | New therapies for recurrent glioblastomas |
title_full | New therapies for recurrent glioblastomas |
title_fullStr | New therapies for recurrent glioblastomas |
title_full_unstemmed | New therapies for recurrent glioblastomas |
title_short | New therapies for recurrent glioblastomas |
title_sort | new therapies for recurrent glioblastomas |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948331/ https://www.ncbi.nlm.nih.gov/pubmed/20948683 http://dx.doi.org/10.3410/M1-94 |
work_keys_str_mv | AT wenpatricky newtherapiesforrecurrentglioblastomas |