Evidence map›Paper›PMID 41670784›Full record

ArticleJournal of neuro-oncology2026

High frequency and unique subtypes of meningioma in patients with BAP1 tumor predisposition syndrome.

Kaylee A Ramsey, Lindsey Byrne, Olivia B Taylor, Amr Soliman, Emma Schreiner, Isabella Gray, Alicia Latham, Rania Sheikh, Saman S Ahmadian, Russell R Lonser and 4 more

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Kaylee A RamseyHavener Eye Institute, Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, 400W 12th Ave, Room 225 Wiseman Hall, Columbus, OH , 43210, USA.
Lindsey ByrneDivision of Human Genetics, Department of Internal Medicine, The Ohio State University Columbus, Columbus, OH, USA.
Olivia B TaylorHavener Eye Institute, Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, 400W 12th Ave, Room 225 Wiseman Hall, Columbus, OH , 43210, USA.
Amr SolimanHavener Eye Institute, Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, 400W 12th Ave, Room 225 Wiseman Hall, Columbus, OH , 43210, USA.
Emma SchreinerHavener Eye Institute, Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, 400W 12th Ave, Room 225 Wiseman Hall, Columbus, OH , 43210, USA.
Isabella GrayHavener Eye Institute, Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, 400W 12th Ave, Room 225 Wiseman Hall, Columbus, OH , 43210, USA.
Alicia LathamDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Rania SheikhDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Saman S AhmadianDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Russell R LonserDepartment of Neurological Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Joshua D PalmerDepartment of Radiation Oncology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Maria I CarloDepartment of Medical Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Colleen M CebullaHavener Eye Institute, Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, 400W 12th Ave, Room 225 Wiseman Hall, Columbus, OH , 43210, USA.
Mohamed H Abdel-RahmanHavener Eye Institute, Department of Ophthalmology and Visual Sciences, The Ohio State University Wexner Medical Center, 400W 12th Ave, Room 225 Wiseman Hall, Columbus, OH , 43210, USA. mohamed.abdel-rahman@osumc.edu.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
The Ohio State University Center for Clinical and Translational Science (UL1)UL1TR000090 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2012 to 2013
$7.9M
The Ohio State University Vision Sciences Research Core Program (OSU-VSRCP)P30EY032857 · NEI · OHIO STATE UNIVERSITY · PI Sayoko E Moroi · 2022 to 2026
$3.6M
Spectrum of clinical phenotype of the BAP1-tumor predisposition syndrome (BAP1-TPDS)R01CA255323 · NCI · OHIO STATE UNIVERSITY · PI ABDEL-RAHMAN, MOHAMED H. · 2021 to 2025
$2.9M
Investigating the Role of KEAP1 Germline and Somatic Mutations in Renal Cell CarcinomaK08CA272960 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Maria Carlo · 2023 to 2026
$1.1M
Kidney Cancer Association Trailblazer AwardNCATS NIH HHS 8UL1TR000090-05NCATS NIH HHS UL1 TR000090NCI NIH HHS K08 CA272960NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA255323NCI NIH HHS R01-CA255323NEI NIH HHS P30 EY032857NIH HHS K08-CA272960-02Ohio State University Cancer Center Core Grant 2P30CA016058-40OSU Vision Sciences Research Core Program P30EY032857Research to Prevent Blindness New Chair Challenge Grant
6 · The paper itself

Abstract

purposeBAP1-tumor predisposition syndrome (BAP1-TPDS) is associated with four main cancers: uveal melanoma, cutaneous melanoma, malignant mesothelioma, and renal cell carcinoma. However, additional cancers are found more rarely in BAP1-TPDS patients. The aim of this study was to investigate the association, clinical, and pathologic characteristics of meningioma in BAP1-TPDS.

methodsWe conducted a retrospective chart review of meningiomas in two independent cohorts of patients with germline BAP1 pathogenic or likely pathogenic (P/LP) variants at The Ohio State University Wexner Medical Center and at the Memorial Sloan Kettering Cancer Center from October 1st, 2010 date to April 21st, 2025. Additionally, we conducted a literature review of meningioma case studies for individuals with germline BAP1 (P/LP) variants.

resultsIn a cohort of 237 subjects with BAP1-TPDS, we identified 6.8% (16/237) with a history of meningiomas. The average age of diagnosis was 44.5 years (17–71). For patients with available pathology, 61.5% (8/13) of the tumors were grade 2/3. Patients with available tumor tissue 83.3% (5/6) showed evidence of BAP1 biallelic inactivation. Family history of meningioma was reported in 18.8% (3/16) of patients. Four cases of meningioma were identified during meningioma surveillance imaging, and five cases had recurrences after treatment. Published cases were consistent with the early age of onset, high-grade tumors, and clinical phenotype of tumors.

conclusionThis study provides additional evidence that high-grade brain and spinal meningiomas are part of the clinical spectrum of BAP1-TPDS. Craniospinal imaging surveillance in the BAP1-TPDS population should be considered starting around puberty, enabling early detection and management for individuals with BAP1-TPDS.

Indexed as

Genetic Predisposition to DiseaseMeningeal NeoplasmsMeningiomaTumor Suppressor ProteinsUbiquitin ThiolesteraseAdolescentAdultAgedFemaleFollow-Up StudiesGerm-Line MutationHumansMaleMiddle AgedRetrospective StudiesYoung AdultBAP1 protein, humanTumor Suppressor ProteinsUbiquitin ThiolesteraseBAP1BAP1-TPDSBAP1 tumor predisposition syndromeBRCA associated protein-1Meningioma

Identifiers

PMID41670784
PMCPMC12894157

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.