Molecular and Clinical Stratification of Astroblastomas: Three distinct Fusion-Defined Groups Informing Risk-Adapted Treatment Strategies
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Publication date
2026-04
Authors
Federico, Aniello
Schmitt-Hoffner, Felix
Fonseca, Adriana
Geisemeyer, Neal
Bruckner, Katharina
Mauermann, Monika
Sill, Martin
Stichel, Damian
Sturm, Dominik
Schüller, Ulrich
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Abstract
Background: Astroblastomas are rare brain tumors predominantly affecting children and young adults, for which molecular subtypes and clinical management remain undefined. Methods: We analyzed tumor samples, molecular profiles, and clinical data from 200 patients, classified as “Astroblastoma, MN1-altered” under WHO criteria, using DNA methylation profiling, DNA/RNA profiling/sequencing, and survival analyses. Results: DNA methylation analyses identified 3 groups: Group A (n = 143, characterized by MN1::BEND2 fusions, predominantly supratentorial location, with striking female predominance and favorable survival); Group B (n = 37, epigenetically and transcriptionally closely related to Group A, but characterized by EWSR1::BEND2 fusions, with spinal and infratentorial locations and poor prognosis); and Group C (n = 20, epigenetically and transcriptionally distinct, characterized by MN1::CXXC5 fusions, exclusively supratentorially located, with favorable survival). Progression-free and overall survival were significantly shorter in Group B (5-year PFS 14%; 10-year OS 54%) compared to A (5-year PFS 47%; 10-year OS 89%) and C (5-year PFS 75%; 10-year OS 89%). Radiotherapy improved PFS in Group B (hazard ratio 0.25), while no clear benefit was identified for Groups A and C. Conclusions: Astroblastoma, MN1-altered, comprises 3 molecularly and clinically distinct groups, characterized by different fusion genes, including those without MN1. These new insights, including the identification of potential predictive biomarkers like 14q/16q loss, provide a framework for the development of risk-stratified therapeutic approaches. Importantly, we identified a molecularly defined high-risk group that benefits from radiation therapy. Our findings redefine Astroblastoma as a molecularly diverse tumor type, propose a refined classification, support the development of risk-adapted therapeutic strategies and provide a rational standard of care.
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Federico, A, Schmitt-Hoffner, F, Fonseca, A, Geisemeyer, N, Bruckner, K, Mauermann, M, Sill, M, Stichel, D, Sturm, D, Schüller, U, Tauziede-Espariat, A, Varlet, P, Capper, D, Abdullaev, Z, Schrimpf, D, Selt, F, Williamson, L, Donson, A M, Antonelli, M, Miele, E, Snuderl, M, Brandner, S, Łastowska, M, Van Der Lugt, J, Bunt, J, Kramm, C, Kolenova, A, Raghunathan, A, Wilson, Y, Weintraub, L, Hansford, J R, Spiegl-Kreinecker, S, Aistleitner, B, Baroni, L, Zapotocky, M, Ramaswamy, V, Korshunov, A, Jones, B, Kjaersgaard, M, Kranendonk, M E, Haberler, C, Packer, R J, Jäger, N, Deimling, A V, Sahm, F, Koster, J, Aldape, K, Pfister, S M, Hoff, K V, Gojo, J & Kool, M 2026, 'Molecular and Clinical Stratification of Astroblastomas : Three distinct Fusion-Defined Groups Informing Risk-Adapted Treatment Strategies', Neuro-oncology, vol. 28, no. 4, pp. 1005-1019. https://doi.org/10.1093/neuonc/noaf283