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Molecular classifications of meningiomas improve biological and prognostic stratification, but their complexity can hinder routine implementation, and their treatment implications remain unclear. This study aimed to establish a whole-exome sequencing (WES)–based molecular grading (MG) system, evaluate its prognostic utility, and examine the associations of gross total resection (GTR) and postoperative adjuvant radiotherapy (RT) with recurrence-free survival (RFS). We retrospectively analyzed 456 patients who underwent resection of intracranial meningiomas (1999–2024) with WES-based MG and the prognostic associations of GTR and adjuvant RT for RFS were evaluated within each MG using propensity score–matched analysis. MG A was defined by the presence of NF2 mutation/22q loss and absence of high-risk molecular alterations; MG B by the absence of both NF2 mutation/22q loss and high-risk alterations; and MG C by the presence of high-risk molecular alterations. RFS differed significantly among MG A, B, and C in the entire cohort and in the subset of patients with WHO grade 1 meningiomas (all pairwise FDR-adjusted p values < 0.05). GTR was associated with longer RFS in matched MG B and MG C (both FDR-adjusted p < 0.01), whereas no statistically significant association was observed in MG A. In exploratory analyses, postoperative adjuvant RT was associated with longer RFS in the matched MG B cohort (FDR-adjusted p = 0.005), whereas analyses in MG A and MG C were inconclusive. This simplified WES-based grading system stratified RFS and enabled exploratory evaluation of treatment-associated outcomes within molecular subgroups.
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Sakai et al. (2026) studied this question.
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