Cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome

Integrins αvβ3 and αvβ5 regulate angiogenesis and invasiveness in cancer, potentially by modulating activation of the transforming growth factor (TGF)-β pathway. The randomized phase III CENTRIC and phase II CORE trials explored the integrin inhibitor cilengitide in patients with newly diagnosed gli...

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Main Authors: Weller, Michael, Nabors, Louis Burt, Gorlia, Thierry, Leske, Henning, Rushing, Elisabeth, Bady, Pierre, Hicking, Christine, Perry, James, Hong, Yong-Kil, Roth, Patrick, Wick, Wolfgang, Goodman, Simon L., Hegi, Monika E., Picard, Martin, Moch, Holger, Straub, Josef, Stupp, Roger
Format: Online
Language:English
Published: Impact Journals LLC 2016
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924768/
id pubmed-4924768
recordtype oai_dc
spelling pubmed-49247682016-07-13 Cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome Weller, Michael Nabors, Louis Burt Gorlia, Thierry Leske, Henning Rushing, Elisabeth Bady, Pierre Hicking, Christine Perry, James Hong, Yong-Kil Roth, Patrick Wick, Wolfgang Goodman, Simon L. Hegi, Monika E. Picard, Martin Moch, Holger Straub, Josef Stupp, Roger Research Paper Integrins αvβ3 and αvβ5 regulate angiogenesis and invasiveness in cancer, potentially by modulating activation of the transforming growth factor (TGF)-β pathway. The randomized phase III CENTRIC and phase II CORE trials explored the integrin inhibitor cilengitide in patients with newly diagnosed glioblastoma with versus without O6-methylguanine DNA methyltransferase (MGMT) promoter methylation. These trials failed to meet their primary endpoints. Impact Journals LLC 2016-02-22 /pmc/articles/PMC4924768/ /pubmed/26918452 http://dx.doi.org/10.18632/oncotarget.7588 Text en Copyright: © 2016 Weller et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Weller, Michael
Nabors, Louis Burt
Gorlia, Thierry
Leske, Henning
Rushing, Elisabeth
Bady, Pierre
Hicking, Christine
Perry, James
Hong, Yong-Kil
Roth, Patrick
Wick, Wolfgang
Goodman, Simon L.
Hegi, Monika E.
Picard, Martin
Moch, Holger
Straub, Josef
Stupp, Roger
spellingShingle Weller, Michael
Nabors, Louis Burt
Gorlia, Thierry
Leske, Henning
Rushing, Elisabeth
Bady, Pierre
Hicking, Christine
Perry, James
Hong, Yong-Kil
Roth, Patrick
Wick, Wolfgang
Goodman, Simon L.
Hegi, Monika E.
Picard, Martin
Moch, Holger
Straub, Josef
Stupp, Roger
Cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome
author_facet Weller, Michael
Nabors, Louis Burt
Gorlia, Thierry
Leske, Henning
Rushing, Elisabeth
Bady, Pierre
Hicking, Christine
Perry, James
Hong, Yong-Kil
Roth, Patrick
Wick, Wolfgang
Goodman, Simon L.
Hegi, Monika E.
Picard, Martin
Moch, Holger
Straub, Josef
Stupp, Roger
author_sort Weller, Michael
title Cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome
title_short Cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome
title_full Cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome
title_fullStr Cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome
title_full_unstemmed Cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome
title_sort cilengitide in newly diagnosed glioblastoma: biomarker expression and outcome
description Integrins αvβ3 and αvβ5 regulate angiogenesis and invasiveness in cancer, potentially by modulating activation of the transforming growth factor (TGF)-β pathway. The randomized phase III CENTRIC and phase II CORE trials explored the integrin inhibitor cilengitide in patients with newly diagnosed glioblastoma with versus without O6-methylguanine DNA methyltransferase (MGMT) promoter methylation. These trials failed to meet their primary endpoints.
publisher Impact Journals LLC
publishDate 2016
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4924768/
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