Machine learning integrates imaging and intraoperative flow cytometry to enhance glioma molecular subtype diagnosis, suggesting improved surgical outcomes.
Introduction Accurate intraoperative identification of glioma molecular subtypes, such as isocitrate dehydrogenase mutation and 1p/19q co-deletion, is essential for precise diagnosis, prognostication, and determining the extent of tumor resection—balancing maximal tumor removal with preservation of neurological function. Methods We developed a machine learning model that integrates preoperative imaging features [magnetic resonance imaging, computed tomography, and 11 C-methionine positron emission tomography (PET)] and intraoperative flow cytometry (iFC) data to predict molecular subtypes of glioma in real-time. Results Analyzing 288 cases of diffuse gliomas, this model achieved an overall accuracy of 76.0%, with a macro-average ROC-AUC of 0.88 and a micro-average ROC-AUC of 0.89. Key predictive factors included the tumor-to-normal uptake ratio on PET, malignancy index from iFC, and patient age, all of which showed significant differences between correctly and incorrectly classified cases. We also developed a prototype application that visualizes the prediction results intraoperatively, thereby supporting real-time surgical decision-making. Conclusion This integrated approach enhances the precision of intraoperative molecular diagnosis and has the potential to optimize surgical strategies for glioma treatment.
No takes yet. Share an insight, caveat, or question.
Koriyama et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: