A MAGIBU-based model for pediatric and juvenile CNS tumors: an in-house epigenetic decision-support framework compared with online DNA methylation classifiers
DOI:
https://doi.org/10.17879/freeneuropathology-2026-9648Keywords:
DNA methylation, Central nervous system, Tumor, Children, Epigenetic, Brain, MAGIBUAbstract
Background: DNA methylation profiling is a tool that provides key support for central nervous system (CNS) tumor classification. However, diagnostically ambiguous pediatric cases may result in discordant outputs across classifiers. We developed MAGIBU, a cross-platform, projection-based framework that embeds individual methylomes into a fixed CNS reference landscape, ranking diagnostic entities by local epigenetic proximity to support clinician-led integrative diagnosis.
Methods: As a proof-of-concept, we evaluated MAGIBU in eight morphologically challenging pediatric/juvenile CNS tumors with unresolved diagnoses after institutional and central pathology review. To establish a benchmark in the absence of a definitive histopathological ground truth, a consensus epigenetic reference was defined a priori for cases showing concordant results between the Heidelberg CNS Tumor Methylation Classifier and Methylscape Analysis. Comparisons were also performed with Epigenomic Digital Pathology (EpiDiP). To validate MAGIBU beyond this discovery cohort, performance was assessed across four independent cohorts
(n = 670), restricted to the diagnostic categories represented in the study framework, specifically low-grade glioma and diffuse midline glioma.
Results: In the discovery cohort, MAGIBU achieved high concordance with the consensus reference (Cohen’s κ = 0.855), outperforming EpiDiP (κ = 0.278), which frequently placed low-grade tumors in proximity to higher-grade reference regions. Extended validation across four independent cohorts (n = 670) demonstrated consistent performance within the diagnostic categories represented in the study framework, with class-level recall ranging from 96.1 % to 99.8 % for low-grade glioma and diffuse midline glioma categories
Conclusions: MAGIBU provides a stable, quantitative differential diagnosis framework that mitigates the limitations of rigid categorical assignments. By leveraging a distance-based proximity metric, it offers a transparent decision-support tool that integrates effectively with clinical, radiological, and molecular data. While performance is inherently dependent on reference atlas composition, MAGIBU represents a robust complementary approach for the diagnostic workup of ambiguous CNS tumors.
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Copyright (c) 2026 Gianluca Mattei, Laura Giunti, Mirko Scagnet, Rina Agushi, Federico Mussa, Chiara Caporalini, Iacopo Sardi, Vincenzo Yuto Civale, Alberto Magi, Lorenzo Genitori, Anna Maria Buccoliero

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