Evidence map›Paper›PMID 42400710›Full record

ArticleDiscover oncology2026

Tumor location and morphological MRI features in relation to combined 1p/22q deletion in meningioma.

Alim Emre Basaran, Laura Wolter, Max Braune, Alonso-Barrantes Freer, Wolf C Müller, Erdem Güresir, Johannes Wach

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Article in Discover 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Alim Emre BasaranDepartment of Neurosurgery, University Hospital Leipzig, University of Leipzig, Liebigstr. 20, 04103, Leipzig, Germany. alim.basaran@medizin.uni-leipzig.de.ORCID http://orcid.org/0009-0006-6872-5528
Laura WolterDepartment of Neurosurgery, University Hospital Leipzig, University of Leipzig, Liebigstr. 20, 04103, Leipzig, Germany.
Max BraunePaul-Flechsig-Institute of Neuropathology, University Hospital Leipzig, 04103, Leipzig, Germany.
Alonso-Barrantes FreerPaul-Flechsig-Institute of Neuropathology, University Hospital Leipzig, 04103, Leipzig, Germany.
Wolf C MüllerPaul-Flechsig-Institute of Neuropathology, University Hospital Leipzig, 04103, Leipzig, Germany.
Erdem GüresirDepartment of Neurosurgery, University Hospital Leipzig, University of Leipzig, Liebigstr. 20, 04103, Leipzig, Germany.
Johannes WachDepartment of Neurosurgery, University Hospital Leipzig, University of Leipzig, Liebigstr. 20, 04103, Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCombined chromosomal 1p/22q deletion is associated with aggressive tumor biology and an increased risk of recurrence in meningiomas. Since C-IMPACT-NOW Update 8, this molecular alteration has gained relevance in the stratification of WHO grade 2 tumors. However, reliable preoperative predictors of combined 1p/22q deletion remain limited. The present study aimed to identify clinical and radiological predictors of combined 1p/22q deletion in meningiomas.

methodsIn this retrospective single-center study, 197 patients with histopathologically confirmed meningiomas and available chromosomal status were analyzed. Preoperative MRI-based tumor characteristics, including tumor volume, surface area, roundness, flatness, and length of dural attachment, were assessed on gadolinium-enhanced T1-weighted MRI. Tumor volumetry was performed using the SmartBrush tool within the BrainLAB software (BrainLAB, Munich, Germany) via a semi-automatic segmentation flow. Surface area, roundness and flatness were derived using the open-source software 3D Slicer. Optimal cut-off values were determined using receiver operating characteristic (ROC) curve analysis with the Youden index. Variables were evaluated using uni- and multivariable analyses. Anatomical subgroup analysis was performed in non-skull base (NSB) meningiomas.

resultsIn the overall cohort, NSB location was independently associated with combined 1p/22q deletion (OR 3.267, 95% CI 1.012-10.545; p = 0.048). In the NSB subgroup (n = 102), tumor volume (p = 0.027), tumor surface area (p = 0.020), and length of dural attachment (p = 0.042) were significantly associated with combined 1p/22q deletion in univariate analyses.

conclusionNSB meningiomas are independently associated with combined 1p/22q deletion. Quantitative and anatomically interpretable MRI-based tumor characteristics, particularly in NSB tumors, may provide supplementary information for preoperative risk stratification. These characteristics may contribute to decision-making process and identifying those necessitating surgery due to potential aggressive biological behavior.

Identifiers

PMID42400710
PMCPMC13332919

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