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Contrasts in Glioblastoma—Venous Thromboembolism versus Bleeding Risk

Glioblastoma is among the tumor entities with an extreme thrombogenic potential and patients are at very high risk of developing a venous thromboembolism (VTE) over the course of the disease, with an incidence of up to 30% per year. Major efforts are currently being made to understand and gain novel...

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Detalles Bibliográficos
Autores principales: Muster, Viktoria, Gary, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228034/
https://www.ncbi.nlm.nih.gov/pubmed/34200229
http://dx.doi.org/10.3390/cells10061414
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author Muster, Viktoria
Gary, Thomas
author_facet Muster, Viktoria
Gary, Thomas
author_sort Muster, Viktoria
collection PubMed
description Glioblastoma is among the tumor entities with an extreme thrombogenic potential and patients are at very high risk of developing a venous thromboembolism (VTE) over the course of the disease, with an incidence of up to 30% per year. Major efforts are currently being made to understand and gain novel insights into the underlying pathomechanisms of the development of VTE in patients with glioblastoma and to find appropriate biomarkers. Yet, patients with glioblastoma not only face a high thromboembolic risk but are also at risk of bleeding events. In the case of VTE, a therapeutic anticoagulation with low molecular weight heparin or, in the case of low bleeding risk, treatment with a direct oral anticoagulant, is recommended, according to recently published guidelines. With respect to an elevated bleeding risk in glioblastoma patients, therapeutic anticoagulation remains challenging in this patient group and prospective data for this vulnerable patient group are scarce, particularly with regard to direct oral anticoagulants.
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spelling pubmed-82280342021-06-26 Contrasts in Glioblastoma—Venous Thromboembolism versus Bleeding Risk Muster, Viktoria Gary, Thomas Cells Review Glioblastoma is among the tumor entities with an extreme thrombogenic potential and patients are at very high risk of developing a venous thromboembolism (VTE) over the course of the disease, with an incidence of up to 30% per year. Major efforts are currently being made to understand and gain novel insights into the underlying pathomechanisms of the development of VTE in patients with glioblastoma and to find appropriate biomarkers. Yet, patients with glioblastoma not only face a high thromboembolic risk but are also at risk of bleeding events. In the case of VTE, a therapeutic anticoagulation with low molecular weight heparin or, in the case of low bleeding risk, treatment with a direct oral anticoagulant, is recommended, according to recently published guidelines. With respect to an elevated bleeding risk in glioblastoma patients, therapeutic anticoagulation remains challenging in this patient group and prospective data for this vulnerable patient group are scarce, particularly with regard to direct oral anticoagulants. MDPI 2021-06-07 /pmc/articles/PMC8228034/ /pubmed/34200229 http://dx.doi.org/10.3390/cells10061414 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Muster, Viktoria
Gary, Thomas
Contrasts in Glioblastoma—Venous Thromboembolism versus Bleeding Risk
title Contrasts in Glioblastoma—Venous Thromboembolism versus Bleeding Risk
title_full Contrasts in Glioblastoma—Venous Thromboembolism versus Bleeding Risk
title_fullStr Contrasts in Glioblastoma—Venous Thromboembolism versus Bleeding Risk
title_full_unstemmed Contrasts in Glioblastoma—Venous Thromboembolism versus Bleeding Risk
title_short Contrasts in Glioblastoma—Venous Thromboembolism versus Bleeding Risk
title_sort contrasts in glioblastoma—venous thromboembolism versus bleeding risk
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228034/
https://www.ncbi.nlm.nih.gov/pubmed/34200229
http://dx.doi.org/10.3390/cells10061414
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