Cancer Medicine (Mar 2023)

Deep learning‐based pathology image analysis predicts cancer progression risk in patients with oral leukoplakia

  • Xinyi Zhang,
  • Frederico O. Gleber‐Netto,
  • Shidan Wang,
  • Roberta Rayra Martins‐Chaves,
  • Ricardo Santiago Gomez,
  • Nadarajah Vigneswaran,
  • Arunangshu Sarkar,
  • William N. William Jr,
  • Vassiliki Papadimitrakopoulou,
  • Michelle Williams,
  • Diana Bell,
  • Doreen Palsgrove,
  • Justin Bishop,
  • John V. Heymach,
  • Ann M. Gillenwater,
  • Jeffrey N. Myers,
  • Renata Ferrarotto,
  • Scott M. Lippman,
  • Curtis Rg Pickering,
  • Guanghua Xiao

DOI
https://doi.org/10.1002/cam4.5478
Journal volume & issue
Vol. 12, no. 6
pp. 7508 – 7518

Abstract

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Abstract Background Oral leukoplakia (OL) is associated with an increased risk for oral cancer (OC) development. Prediction of OL cancer progression may contribute to decreased OC morbidity and mortality by favoring early intervention. Current OL progression risk assessment approaches face large interobserver variability and is weakly prognostic. We hypothesized that convolutional neural networks (CNN)‐based histology image analyses could accelerate the discovery of better OC progression risk models. Methods Our CNN‐based oral mucosa risk stratification model (OMRS) was trained to classify a set of nondysplastic oral mucosa (OM) and a set of OC H&E slides. As a result, the OMRS model could identify abnormal morphological features of the oral epithelium. By applying this model to OL slides, we hypothesized that the extent of OC‐like features identified in the OL epithelium would correlate with its progression risk. The OMRS model scored and categorized the OL cohort (n = 62) into high‐ and low‐risk groups. Results OL patients classified as high‐risk (n = 31) were 3.98 (95% CI 1.36–11.7) times more likely to develop OC than low‐risk ones (n = 31). Time‐to‐progression significantly differed between high‐ and low‐risk groups (p = 0.003). The 5‐year OC development probability was 21.3% for low‐risk and 52.5% for high‐risk patients. The predictive power of the OMRS model was sustained even after adjustment for age, OL site, and OL dysplasia grading (HR = 4.52, 1.5–13.7). Conclusion The ORMS model successfully identified OL patients with a high risk of OC development and can potentially benefit OC early diagnosis and prevention policies.

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