Fast intraoperative detection of primary central nervous system lymphoma and differentiation from common central nervous system tumors using stimulated Raman histology and deep learning
- PMID: 39673805
- PMCID: PMC12187372
- DOI: 10.1093/neuonc/noae270
Fast intraoperative detection of primary central nervous system lymphoma and differentiation from common central nervous system tumors using stimulated Raman histology and deep learning
Abstract
Background: Accurate intraoperative diagnosis is crucial for differentiating between primary central nervous system (CNS) lymphoma (PCNSL) and other CNS entities, guiding surgical decision-making, but represents significant challenges due to overlapping histomorphological features, time constraints, and differing treatment strategies. We combined stimulated Raman histology (SRH) with deep learning to address this challenge.
Methods: We imaged unprocessed, label-free tissue samples intraoperatively using a portable Raman scattering microscope, generating virtual H&E-like images within <3 min. We developed a deep learning pipeline called RapidLymphoma based on a self-supervised learning strategy to (1) detect PCNSL, (2) differentiate from other CNS entities, and (3) test the diagnostic performance in a prospective international multicenter cohort and 2 additional independent test cohorts. We trained on 54 000 SRH patch images sourced from surgical resections and stereotactic-guided biopsies, including various CNS neoplastic/nonneoplastic lesions. Training and test data were collected from 4 tertiary international medical centers. The final histopathological diagnosis served as ground truth.
Results: In the prospective test cohort of PCNSL and non-PCNSL entities (n = 160), RapidLymphoma achieved an overall balanced accuracy of 97.81% ± 0.91, non-inferior to frozen section analysis in detecting PCNSL (100% vs. 77.77%). The additional test cohorts (n = 420, n = 59) reached balanced accuracy rates of 95.44% ± 0.74 and 95.57% ± 2.47 in differentiating IDH-wildtype diffuse gliomas and various brain metastasis from PCNSL. Visual heatmaps revealed RapidLymphoma's capabilities to detect class-specific histomorphological key features.
Conclusions: RapidLymphoma proves reliable and valid for intraoperative PCNSL detection and differentiation from other CNS entities. It provides visual feedback within 3 min, enabling fast clinical decision-making and subsequent treatment strategy planning.
Keywords: artificial intelligence; brain tumor; deep learning; intraoperative histopathology; optical imaging; primary CNS lymphoma; stimulated Raman histology.
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Conflict of interest statement
D.A.O and T.C.H. are shareholders in Invenio Imaging, Inc. M.S. is a scientific advisor and shareholder of Heidelberg Epignostix and Halo Dx, and a scientific advisor of Arima Genomics, and InnoSIGN, and received research funding from Lilly USA, not related to this work. All other authors do not have any competing interests.
Update of
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Fast intraoperative detection of primary CNS lymphoma and differentiation from common CNS tumors using stimulated Raman histology and deep learning.medRxiv [Preprint]. 2024 Aug 26:2024.08.25.24312509. doi: 10.1101/2024.08.25.24312509. medRxiv. 2024. Update in: Neuro Oncol. 2025 Jun 21;27(5):1297-1310. doi: 10.1093/neuonc/noae270. PMID: 39252932 Free PMC article. Updated. Preprint.
Comment in
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When machines start examining tissue specimens on their own.Neuro Oncol. 2025 Jun 21;27(5):1311-1312. doi: 10.1093/neuonc/noaf021. Neuro Oncol. 2025. PMID: 39864074 No abstract available.
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