Prognostic role of Ki-67 in glioblastomas excluding contribution from non-neoplastic cells

Abstract Survival of glioblastoma patients varies and prognostic markers are important in the clinical setting. With digital pathology and improved immunohistochemical multiplexing becoming a part of daily diagnostics, we investigated the prognostic value of the Ki-67 labelling index (LI) in gliobla...

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Autores principales: Rikke H. Dahlrot, Julie A. Bangsø, Jeanette K. Petersen, Ann Mari Rosager, Mia D. Sørensen, Guido Reifenberger, Steinbjørn Hansen, Bjarne W. Kristensen
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/e9d2b1e38f8143a7b7f811815123cf89
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spelling oai:doaj.org-article:e9d2b1e38f8143a7b7f811815123cf892021-12-02T17:41:12ZPrognostic role of Ki-67 in glioblastomas excluding contribution from non-neoplastic cells10.1038/s41598-021-95958-92045-2322https://doaj.org/article/e9d2b1e38f8143a7b7f811815123cf892021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-95958-9https://doaj.org/toc/2045-2322Abstract Survival of glioblastoma patients varies and prognostic markers are important in the clinical setting. With digital pathology and improved immunohistochemical multiplexing becoming a part of daily diagnostics, we investigated the prognostic value of the Ki-67 labelling index (LI) in glioblastomas more precisely than previously by excluding proliferation in non-tumor cells from the analysis. We investigated the Ki-67 LI in a well-annotated population-based glioblastoma patient cohort (178 IDH-wildtype, 3 IDH-mutated). Ki-67 was identified in full tumor sections with automated digital image analysis and the contribution from non-tumor cells was excluded using quantitative double-immunohistochemistry. For comparison of the Ki-67 LI between WHO grades (II-IV), 9 IDH-mutated diffuse astrocytomas and 9 IDH-mutated anaplastic astrocytomas were stained. Median Ki-67 LI increased with increasing WHO grade (median 2.7%, 6.4% and 27.5%). There was no difference in median Ki-67 LI between IDH-mutated and IDH-wildtype glioblastomas (p = 0.9) and Ki-67 LI was not associated with survival in glioblastomas in neither univariate (p = 0.9) nor multivariate analysis including MGMT promoter methylation status and excluding IDH-mutated glioblastomas (p = 0.2). Ki-67 may be of value in the differential diagnostic setting, but it must not be over-interpreted in the clinico-pathological context.Rikke H. DahlrotJulie A. BangsøJeanette K. PetersenAnn Mari RosagerMia D. SørensenGuido ReifenbergerSteinbjørn HansenBjarne W. KristensenNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Rikke H. Dahlrot
Julie A. Bangsø
Jeanette K. Petersen
Ann Mari Rosager
Mia D. Sørensen
Guido Reifenberger
Steinbjørn Hansen
Bjarne W. Kristensen
Prognostic role of Ki-67 in glioblastomas excluding contribution from non-neoplastic cells
description Abstract Survival of glioblastoma patients varies and prognostic markers are important in the clinical setting. With digital pathology and improved immunohistochemical multiplexing becoming a part of daily diagnostics, we investigated the prognostic value of the Ki-67 labelling index (LI) in glioblastomas more precisely than previously by excluding proliferation in non-tumor cells from the analysis. We investigated the Ki-67 LI in a well-annotated population-based glioblastoma patient cohort (178 IDH-wildtype, 3 IDH-mutated). Ki-67 was identified in full tumor sections with automated digital image analysis and the contribution from non-tumor cells was excluded using quantitative double-immunohistochemistry. For comparison of the Ki-67 LI between WHO grades (II-IV), 9 IDH-mutated diffuse astrocytomas and 9 IDH-mutated anaplastic astrocytomas were stained. Median Ki-67 LI increased with increasing WHO grade (median 2.7%, 6.4% and 27.5%). There was no difference in median Ki-67 LI between IDH-mutated and IDH-wildtype glioblastomas (p = 0.9) and Ki-67 LI was not associated with survival in glioblastomas in neither univariate (p = 0.9) nor multivariate analysis including MGMT promoter methylation status and excluding IDH-mutated glioblastomas (p = 0.2). Ki-67 may be of value in the differential diagnostic setting, but it must not be over-interpreted in the clinico-pathological context.
format article
author Rikke H. Dahlrot
Julie A. Bangsø
Jeanette K. Petersen
Ann Mari Rosager
Mia D. Sørensen
Guido Reifenberger
Steinbjørn Hansen
Bjarne W. Kristensen
author_facet Rikke H. Dahlrot
Julie A. Bangsø
Jeanette K. Petersen
Ann Mari Rosager
Mia D. Sørensen
Guido Reifenberger
Steinbjørn Hansen
Bjarne W. Kristensen
author_sort Rikke H. Dahlrot
title Prognostic role of Ki-67 in glioblastomas excluding contribution from non-neoplastic cells
title_short Prognostic role of Ki-67 in glioblastomas excluding contribution from non-neoplastic cells
title_full Prognostic role of Ki-67 in glioblastomas excluding contribution from non-neoplastic cells
title_fullStr Prognostic role of Ki-67 in glioblastomas excluding contribution from non-neoplastic cells
title_full_unstemmed Prognostic role of Ki-67 in glioblastomas excluding contribution from non-neoplastic cells
title_sort prognostic role of ki-67 in glioblastomas excluding contribution from non-neoplastic cells
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/e9d2b1e38f8143a7b7f811815123cf89
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