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Histopathological predictors of progression-free survival in atypical meningioma: a single-center retrospective cohort and meta-analysis.

Authors :
Kim MS
Chun SW
Dho YS
Seo Y
Lee JH
Won JK
Kim JW
Park CK
Park SH
Kim YH
Source :
Brain tumor pathology [Brain Tumor Pathol] 2022 Apr; Vol. 39 (2), pp. 99-110. Date of Electronic Publication: 2022 Jan 15.
Publication Year :
2022

Abstract

To determine the prognostic significance of histopathological features included in the diagnostic criteria of atypical meningioma for progression-free survival (PFS). We performed a retrospective cohort study and meta-analysis. Brain invasion, mitotic index, spontaneous necrosis, sheeting, prominent nucleoli, high cellularity, and small cells were the histopathological features of interest. The data from 25 studies involving 3590 patients including our cohort (nā€‰=ā€‰262) were included. The pooled HR of mitotic index at a cutoff value of 4 showed no statical significance in the gross analysis (pooled HR, 1.09; 95% CI 0.61-1.96; pā€‰=ā€‰0.7699). Furthermore, it failed to prognosticate PFS in other pooled analyses. For brain invasion, no consistent association with the progression was found in each pooled analysis according to the included studies. Among the remaining five atypical features, spontaneous necrosis, sheeting, and prominent nucleoli showed a significant correlation with PFS in the gross analysis. In the analysis that pooled the HRs from the multivariate analyses, only spontaneous necrosis had significant association with PFS. The available evidence supports that the current cutoff value of mitotic index for diagnosing atypical meningioma might be improper to have prognostic value. The prognostic significance of brain invasion also needs further evaluation.<br /> (© 2021. The Author(s) under exclusive licence to The Japan Society of Brain Tumor Pathology.)

Details

Language :
English
ISSN :
1861-387X
Volume :
39
Issue :
2
Database :
MEDLINE
Journal :
Brain tumor pathology
Publication Type :
Academic Journal
Accession number :
35031884
Full Text :
https://doi.org/10.1007/s10014-021-00419-w