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Increased proliferation is associated with CNS invasion in meningiomas

INTRODUCTION: Meningiomas are the most common benign intracranial neoplasms. CNS invasion in meningiomas has been integrated into the 2016 WHO classification of CNS tumors as a stand-alone criterion for atypia. Since then, its prognostic impact has been debated based on contradictory results from re...

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Autores principales: Behling, Felix, Fodi, Christina, Wang, Sophie, Hempel, Johann-Martin, Hoffmann, Elgin, Tabatabai, Ghazaleh, Honegger, Jürgen, Tatagiba, Marcos, Schittenhelm, Jens, Skardelly, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651603/
https://www.ncbi.nlm.nih.gov/pubmed/34800210
http://dx.doi.org/10.1007/s11060-021-03892-7
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author Behling, Felix
Fodi, Christina
Wang, Sophie
Hempel, Johann-Martin
Hoffmann, Elgin
Tabatabai, Ghazaleh
Honegger, Jürgen
Tatagiba, Marcos
Schittenhelm, Jens
Skardelly, Marco
author_facet Behling, Felix
Fodi, Christina
Wang, Sophie
Hempel, Johann-Martin
Hoffmann, Elgin
Tabatabai, Ghazaleh
Honegger, Jürgen
Tatagiba, Marcos
Schittenhelm, Jens
Skardelly, Marco
author_sort Behling, Felix
collection PubMed
description INTRODUCTION: Meningiomas are the most common benign intracranial neoplasms. CNS invasion in meningiomas has been integrated into the 2016 WHO classification of CNS tumors as a stand-alone criterion for atypia. Since then, its prognostic impact has been debated based on contradictory results from retrospective analyses. The aim of the study was to elucidate whether histopathological evidence of CNS invasion is associated with increased proliferative potential. METHODS: We have conducted a quantified measurement of the proliferation marker Ki67 and analyzed its association with CNS invasion determined by histology together with other established prognostic markers of progression. Routine, immunohistochemical staining for Ki67 were digitalized and automatic quantification was done using Image J software. RESULTS: Overall, 1718 meningiomas were assessed. Histopathological CNS invasion was seen in 108 cases (6.7%). Uni- and multivariate analysis revealed a significantly higher Ki67 proliferation rate in meningiomas with CNS invasion (p < 0.0001 and p = 0.0098, respectively). CONCLUSIONS: Meningiomas with histopathological CNS invasion show a higher proliferative activity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11060-021-03892-7.
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spelling pubmed-86516032021-12-08 Increased proliferation is associated with CNS invasion in meningiomas Behling, Felix Fodi, Christina Wang, Sophie Hempel, Johann-Martin Hoffmann, Elgin Tabatabai, Ghazaleh Honegger, Jürgen Tatagiba, Marcos Schittenhelm, Jens Skardelly, Marco J Neurooncol Laboratory Investigation INTRODUCTION: Meningiomas are the most common benign intracranial neoplasms. CNS invasion in meningiomas has been integrated into the 2016 WHO classification of CNS tumors as a stand-alone criterion for atypia. Since then, its prognostic impact has been debated based on contradictory results from retrospective analyses. The aim of the study was to elucidate whether histopathological evidence of CNS invasion is associated with increased proliferative potential. METHODS: We have conducted a quantified measurement of the proliferation marker Ki67 and analyzed its association with CNS invasion determined by histology together with other established prognostic markers of progression. Routine, immunohistochemical staining for Ki67 were digitalized and automatic quantification was done using Image J software. RESULTS: Overall, 1718 meningiomas were assessed. Histopathological CNS invasion was seen in 108 cases (6.7%). Uni- and multivariate analysis revealed a significantly higher Ki67 proliferation rate in meningiomas with CNS invasion (p < 0.0001 and p = 0.0098, respectively). CONCLUSIONS: Meningiomas with histopathological CNS invasion show a higher proliferative activity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11060-021-03892-7. Springer US 2021-11-20 2021 /pmc/articles/PMC8651603/ /pubmed/34800210 http://dx.doi.org/10.1007/s11060-021-03892-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Laboratory Investigation
Behling, Felix
Fodi, Christina
Wang, Sophie
Hempel, Johann-Martin
Hoffmann, Elgin
Tabatabai, Ghazaleh
Honegger, Jürgen
Tatagiba, Marcos
Schittenhelm, Jens
Skardelly, Marco
Increased proliferation is associated with CNS invasion in meningiomas
title Increased proliferation is associated with CNS invasion in meningiomas
title_full Increased proliferation is associated with CNS invasion in meningiomas
title_fullStr Increased proliferation is associated with CNS invasion in meningiomas
title_full_unstemmed Increased proliferation is associated with CNS invasion in meningiomas
title_short Increased proliferation is associated with CNS invasion in meningiomas
title_sort increased proliferation is associated with cns invasion in meningiomas
topic Laboratory Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8651603/
https://www.ncbi.nlm.nih.gov/pubmed/34800210
http://dx.doi.org/10.1007/s11060-021-03892-7
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