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Molecular and clinical stratification of astroblastomas: Three distinct fusion-defined groups informing risk-adapted treatment strategies

  • Aniello Federico
  • , Felix Schmitt-Hoffner
  • , Adriana Fonseca
  • , Neal Geisemeyer
  • , Katharina Bruckner
  • , Monika Mauermann
  • , Martin Sill
  • , Damian Stichel
  • , Dominik Sturm
  • , Ulrich Schüller
  • , Arnault Tauziede-Espariat
  • , Pascale Varlet
  • , David Capper
  • , Zied Abdullaev
  • , Daniel Schrimpf
  • , Florian Selt
  • , Lane Williamson
  • , Andrew M. Donson
  • , Manila Antonelli
  • , Evelina Miele
  • Matija Snuderl, Sebastian Brandner, Maria Łastowska, Jasper van der Lugt, Jens Bunt, Christof Kramm, Alexandra Kolenova, Aditya Raghunathan, Yelena Wilson, Lauren Weintraub, Jordan R. Hansford, Sabine Spiegl-Kreinecker, Barbara Aistleitner, Lorena Baroni, Michal Zapotocky, Vijay Ramaswamy, Andrey Korshunov, Barbara Jones, Mimi Kjaersgaard, Mariëtte E. Kranendonk, Christine Haberler, Roger J. Packer, Natalie Jäger, Andreas von Deimling, Felix Sahm, Jan Koster, Kenneth Aldape, Stefan M. Pfister, Katja von Hoff, Johannes Gojo, Marcel Kool

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

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.

Original languageEnglish
Pages (from-to)1005-1019
Number of pages15
JournalNeuro-Oncology
Volume28
Issue number4
DOIs
Publication statusPublished - Apr 2026

Keywords

  • EWSR1::BEND2
  • MN1-altered
  • MN1::BEND2
  • MN1::CXXC5
  • astroblastoma
  • gene fusion
  • Neoplasms, Neuroepithelial/genetics
  • Prognosis
  • Follow-Up Studies
  • Humans
  • Middle Aged
  • Child, Preschool
  • Male
  • Biomarkers, Tumor/genetics
  • Young Adult
  • DNA Methylation
  • Female
  • Adult
  • Oncogene Proteins, Fusion/genetics
  • Child
  • Trans-Activators
  • Survival Rate
  • Brain Neoplasms/genetics
  • Tumor Suppressor Proteins/genetics
  • Adolescent
  • Aged

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