Foundation models for fast, label-free detection of glioma infiltration
A critical challenge in glioma treatment is detecting tumour infiltration during surgery to achieve safe maximal resection<sup>1-3</sup>. Unfortunately, safely resectable residual tumour is found in the majority of patients with glioma after surgery, causing early recurrence and decreased survival<sup>4-6</sup>. Here we present FastGlioma, a visual foundation model for fast (<10 s) and accurate detection of glioma infiltration in fresh, unprocessed surgical tissue. FastGlioma was pretrained using large-scale self-supervision (around 4 million images) on rapid, label-free optical microscopy, and fine-tuned to output a normalized score that indicates the degree of tumour infiltration within whole-slide optical images. In a prospective, multicentre, international testing cohort of patients with diffuse glioma (n = 220), FastGlioma was able to detect and quantify the degree of tumour infiltration with an average area under the receiver operating characteristic curve of 92.1 ± 0.9%. FastGlioma outperformed image-guided and fluorescence-guided adjuncts for detecting tumour infiltration during surgery by a wide margin in a head-to-head, prospective study (n = 129). The performance of FastGlioma remained high across diverse patient demographics, medical centres and diffuse glioma molecular subtypes as defined by the World Health Organization. FastGlioma shows zero-shot generalization to other adult and paediatric brain tumour diagnoses, demonstrating the potential for our foundation model to be used as a general-purpose adjunct for guiding brain tumour surgeries. These findings represent the transformative potential of medical foundation models to unlock the role of artificial intelligence in the care of patients with cancer.
Authors
- Christian W. Freudiger
- Akhil Kondepudi (ORCID: https://orcid.org/0000-0002-2643-7580)
- Mitchel Stuart Berger (ORCID: https://orcid.org/0000-0003-1983-4892)
- Edward Harake (ORCID: https://orcid.org/0000-0002-8865-1267)
- Katie Scotford
- Xinhai Hou
- Shawn L. Hervey‐Jumper (ORCID: https://orcid.org/0000-0003-4699-260X)
- Thomas Roetzer-Pejrimovsky (ORCID: https://orcid.org/0000-0001-8875-7304)
- Cheng Jiang (ORCID: https://orcid.org/0000-0003-1759-4960)
- Wajd N. Al‐Holou (ORCID: https://orcid.org/0000-0001-8528-4855)
- Todd Charles Hollon (ORCID: https://orcid.org/0000-0001-5987-6531)
- Aditya S. Pandey (ORCID: https://orcid.org/0000-0003-0789-4273)
- Daniel A. Orringer (ORCID: https://orcid.org/0000-0001-6427-8376)
- Georg Widhalm (ORCID: https://orcid.org/0000-0001-6014-0273)
- Melike Pekmezci (ORCID: https://orcid.org/0000-0003-2548-8359)
- Akshay Rao (ORCID: https://orcid.org/0000-0001-6920-6355)
- Asadur Chowdury (ORCID: https://orcid.org/0000-0002-5653-9721)
- Misha Movahed-Ezazi (ORCID: https://orcid.org/0000-0002-9249-5498)
- Lisa Koerner (ORCID: https://orcid.org/0000-0002-9227-461X)
- Lin Wang (ORCID: https://orcid.org/0000-0002-6449-4930)
- Honglak Lee (ORCID: https://orcid.org/0000-0002-4109-327X)
- P R Lowenstein
- Maria G. Castro
- Sandra Camelo‐Piragua
Institutions
- Rutgers, The State University of New Jersey (US)
- University of California, San Francisco (US)
- University of Michigan (US)
- Invenio Imaging (United States) (US)
- Michigan Medicine (US)
- Neurological Surgery (US)
- New York University (US)
- Medical University of Vienna (AT)
Publication Details
- Journal
- Nature
- Published
- 2024-11-13
- DOI
- https://doi.org/10.1038/s41586-024-08169-3
- Citations
- 59
- Primary Topic
- Glioma Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 25.84