# AI-driven label-free Raman spectromics for intraoperative spinal tumor assessment

**Authors:** David Reinecke, Nina Müller, Anna-Katharina Meissner, Gina Fürtjes, Lili Leyer, Claire Wang, Adrian Ion-Margineanu, Nader Maarouf, Andrew Smith, Todd C. Hollon, Cheng Jiang, Xinhai Hou, Abdulkader Al-Shughri, Lisa I. Körner, Georg Widhalm, Thomas Roetzer-Pejrimovsky, Matija Snuderl, Sandra Camelo-Piragua, John G. Golfinos, Roland Goldbrunner, Daniel A. Orringer, Niklas von Spreckelsen, Volker Neuschmelting

PMC · DOI: 10.1038/s41746-025-02279-6 · NPJ Digital Medicine · 2026-03-17

## TL;DR

A new AI system called SpineXtract enables rapid spinal tumor diagnosis during surgery using Raman spectromics, offering faster and more accurate results than current methods.

## Contribution

The first AI-powered system for intraoperative spinal tumor classification using label-free Raman histology.

## Key findings

- SpineXtract achieved 92.9% macro-average balanced accuracy in classifying spinal tumors within 5 minutes.
- The system outperformed existing brain tumor classifiers by 15.6% in accuracy.
- Performance remained consistent across multiple institutions and tumor types.

## Abstract

Spinal tumor surgery requires rapid tissue diagnosis to guide surgical decisions and further treatment strategies, yet current intraoperative methods are time-intensive and require specialized expertise. No AI systems exist for real-time spinal tumor classification during surgery. We developed SpineXtract, the first AI-powered system for rapid intraoperative spinal tumor diagnosis using stimulated Raman histology (SRH) — a label-free Raman spectromics imaging technique without tissue processing available during surgery. We created a transformer-based classifier optimized for spinal tissue characteristics to identify common tumor types: meningioma, schwannoma, ependymoma, and metastasis. The system was tested in an international, multicenter, simulated, single-arm study using existing SRH datasets (44 patients, 142 slide-images) from three international institutions, with final pathological diagnosis as reference standard. SpineXtract achieved a 92.9% macro-average balanced accuracy (95% CI: 85.5–98.2) within 5 minutes (tumor-specific accuracy range, 84.2–98.6%), while providing quantitative microscopic feedback for granular tissue analysis. Performance remained consistent across institutions (macro balanced accuracy 91.4–92.0%) and outperformed existing brain tumor classifiers by 15.6%. Our results demonstrate clinical applicability, enabling rapid intraoperative diagnosis with performance exceeding current methods, potentially transforming intraoperative diagnostic workflows in spinal tumor surgery.

## Linked entities

- **Diseases:** meningioma (MONDO:0003057), schwannoma (MONDO:0002546), ependymoma (MONDO:0003478)

## Full-text entities

- **Diseases:** SRH (MESH:D009370), Metastatic tumors (MESH:D009369), spinal neoplasm (MESH:D013125), benign nerve sheath tumors (MESH:D018317), Meningioma (MESH:D008579), ewing sarcoma (MESH:D012512), space-occupying lesions (MESH:D008158), bladder (MESH:D001745), breast, and prostate cancer (MESH:D001943), spinal lesion (MESH:D013122), brain tumor (MESH:D001932), lymphomas (MESH:D008223), Metastatic lesion (MESH:D000092182), Schwannoma (MESH:D009442), metastases (MESH:D009362), kidney (MESH:D007674), nerve compression (MESH:D009408), CNS tumor (MESH:D016543), intracranial lesions (MESH:D020765), lung (MESH:D008171), oncological (MESH:D000072716), non-small cell lung cancer (MESH:D002289), spinal astrocytomas (MESH:D001254), esophagus (MESH:D004938), Spinal Ependymoma (MESH:D004806)
- **Chemicals:** H&amp;E (MESH:D006371), formalin (MESH:D005557), paraffin (MESH:D010232), fatty acids (MESH:D005227), acrylic (-), lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12996391/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12996391/full.md

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Source: https://tomesphere.com/paper/PMC12996391