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. 2024 Nov 11;26(Suppl 8):viii312. doi: 10.1093/neuonc/noae165.1238

TMIC-60. BRATS-PATH: ASSESSING HETEROGENEOUS HISTOPATHOLOGIC REGIONS IN GLIOBLASTOMA

Siddhesh Thakur 1, Shahriar Faghani 2, Mana Moassefi 3, Ujjwal Baid 4, Verena Chung 5, Sarthak Pati 6, Shubham Innani 7, Bhakti Baheti 8, Jacob Albrecht 9, Alexandros Karargyris 10, Hasan Kassem 11, Maclean Nasrallah 12, Jared Ahrendsen 13, Valeria Barresi 14, Maria Gubbiotti 15, Giselle Lopez 16, Calixto-Hope Lucas 17, Michael Miller 18, Lee Cooper 19, Jason Huse 20, William Bell 21, Spyridon Bakas 22,23
PMCID: PMC11554170

Abstract

Glioblastoma, the most common malignant primary adult brain tumor, poses significant diagnostic and treatment challenges due to its heterogeneous molecular and micro-environmental profiles. To this end, we organize the BraTS-Path challenge to provide a public benchmarking environment and a comprehensive dataset to develop and validate AI models for identifying distinct histopathologic glioblastoma sub-regions in H&E-stained digitized tissue sections. We identified 188 multi-institutional diagnostic slides of glioblastoma (IDH-wt, Gr.4) cases, from the TCGA-GBM and TCGA-LGG data collections, following their reclassification according to the 2021 WHO classification criteria. Sub-regions were selected according to distinctive morphology of histopathologic features and included aggressive tumor biology and areas consistent with potential treatment effect. Selected sub-region annotations included cellular tumor, geographic necrosis, cortical infiltration, pseudopalisading necrosis, microvascular proliferation, white matter penetration, regions dense with macrophages, leptomeningeal infiltration, and presence of lymphocytes. We obtained 107,340 patches of size 512x512 from the 9 sub-regions. A global network of board-certified expert neuropathologists defined and followed a systematic annotation protocol based on clinical definitions and only delineated sub-regions with high confidence, thus ensuring high-quality standardized data. Each tissue section was assigned to an annotator-approver pair, with the annotator delineating sub-regions and the approver ensuring the consistency of the annotations. By crowdsourcing annotations, the BraTS-Path challenge harnesses the collective expertise of clinical neuropathologists and fosters a collaborative environment to advance the neuro-oncology field. The anticipated developed algorithms are expected to integrate state-of-the-art computational methods, achieving high accuracy in identifying diverse histopathologic features and advancing clinical decision-making processes. The BraTS-Path challenge aims to bridge the gap between research and clinical practice by promoting the development of AI-driven tools for precise tumor characterization. This collaborative effort can significantly enhance our understanding of glioblastoma, improve diagnostic accuracy, and inform treatment strategies, thereby contributing to better patient outcomes.


Articles from Neuro-Oncology are provided here courtesy of Society for Neuro-Oncology and Oxford University Press

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