Incidental meningiomas have favorable clinical outcomes across molecular classification systems
Year: 2026
Type: article
Study design: Observational Study
Abstract: BACKGROUND: Clinical and radiographic models predict incidental meningioma growth, but their molecular architecture is unknown. METHODS: We analyzed serial magnetic resonance imaging, IMPACT groups (Incidental Meningioma: Prognostic Analysis Using Patient Comorbidity and MRI Tests), targeted gene expression, DNA methylation, and copy number (CNA) profiling of 238 consecutive incidental meningiomas from a single neurosurgical center. RESULTS: The cohort was 81% female, with a median age of 59 years at detection and median tumor volume of 3.83 cm³. Symptoms developed in 15.5%; 93.7% were treated (median time-to-treatment 1.06 years), with 5% recurrence. IMPACT groups stratified treatment-free (P < .0001) and symptom-free survival (P = .0007). Most meningiomas were molecularly low risk, although those from the hypermitotic DNA methylation group had higher IMPACT scores (P = .0020). Incidental meningiomas had distinct CNA and gene expression patterns and favorable outcomes compared to 1434 nonincidental meningiomas. CONCLUSIONS: These findings support surveillance for most incidental meningiomas, but early treatment may improve outcomes for molecularly higher-risk cases.
Source: Neuro-Oncology
Institution: University of California, San Francisco
Language: English
Subfield: Epidemiology
Field: Medicine
Domain: Health Sciences
Open Access status: green
Awards: G5340498288, G9000045896, Understanding druggable drivers of meningioma tumorigenesis, UCSF Paul Calabresi K12 Career Development Program in Clinical Oncology, Interplay of tumor genomic and immune characteristics and external drivers of health to improve cancer health outcomes, Mechanistic and Functional Genomic Interrogation of Meningioma Radiotherapy Response Genes
OpenAlex ID: W7154845985
