To explore the use of AI applications in the diagnosis and risk assessment of oral epithelial dysplasia (OED) within the context of a Cancer Research UK-funded project.
Approach:
Research Background: Adam Shephard discusses his transition from neuroimaging to computational pathology, focusing on OED as part of a Cancer Research UK-funded project.
Challenges in Grading OED: The subjective nature of histological grading leads to variability among pathologists and does not reliably predict clinical outcomes.
AI Model Development: HoVer-Net+ was developed to analyze histology images at the nuclear level, extracting biologically meaningful features for predicting cancer risk.
Risk Prediction Importance: AI models aim to improve early detection and treatment by providing consistent risk assessments to support clinical decision-making.
Biomarkers Identification: The study identified new biomarkers, such as increased lymphocyte infiltration, linked to malignant progression.
Performance Comparison: AI-derived biomarkers showed strong agreement with expert pathologists, though performance varied with external datasets.
Multimodal AI Models: Combining histology with clinical data offers a more comprehensive understanding of patient risk factors.
Key Findings:
AI models can provide more consistent risk predictions than traditional histological grading.
New biomarkers linked to cancer risk were identified, enhancing understanding of disease progression.
AI-derived tools achieved performance comparable to expert pathologists in risk assessment.
Interpretation:
AI applications in OED diagnostics may enhance risk assessment and support clinical decision-making.
Limitations:
Variability in performance when tested on external datasets due to differences in clinical practices.
Challenges in collecting consistent clinical data across multiple sites for multimodal studies.
Conclusion:
AI has the potential to improve risk assessment in OED.
An ancillary analysis found less than 2-percentage-point differences in 10-year recurrence across margin thresholds, with no statistically significant adjusted association.