Multidimensional Artificial Intelligence–Based Cancer Progression Prediction in Oral Leukoplakia

医学 癌症 一致性 白斑 概化理论 肿瘤科 分级(工程) 发育不良 内科学 布里氏评分 免疫组织化学 口腔白斑 回顾性队列研究 口腔颌面外科 病理 上皮发育不良 口腔颌面病理学 判别式 转移 肿瘤进展 活检 生存分析 头颈部癌 多元分析 口腔粘膜
作者
John Adeoye,Hongqiu Wang,Anthony W.I. Lo,US Khoo,Yu‐Xiong Su
出处
期刊:Journal of Dental Research [SAGE Publishing]
卷期号:105 (6): 727-736 被引量:2
标识
DOI:10.1177/00220345251378053
摘要

Oral cancer often develops from oral potentially malignant disorders. Oral leukoplakia (OL) is the most common oral potentially malignant disorder. However, not all patients with OL develop oral cancer in their lifetimes, and cancer risk assessment is challenging. This study developed a time-to-event artificial intelligence–based model (termed OralCancerPredict ) that integrated patient characteristics, histologic features, and immunohistochemical indicators for precise prediction of cancer progression in OL. We performed a retrospective analysis of patient data ( n = 456) and tissue samples ( n = 1,312) obtained before cancer progression or at last follow-up for patients with OL. KRT13 and p53 immunohistochemistry and quantitative analyses were performed for tissue samples, while independent prognostic features, including demographic characteristics, clinical information, and histopathologic findings, were obtained for patients in the cohort. KRT13 and p53 expression was combined with histologic and patient data for model training, testing, and external validation. Performance evaluation for OralCancerPredict included model discriminative ability, calibration, explainability, and net benefit analysis via decision curves. External validation was also performed to ensure model generalizability based on patient data ( n = 119) and tissue samples ( n = 322) unused for training and testing. Our findings showed that OralCancerPredict trained on multidimensional data had good concordance indices (0.855 to 0.867), areas under the curve (0.877 to 0.882), and integrated Brier scores (0.046 to 0.069) at testing and external validation. Explainability analysis confirmed the importance of KRT13 and p53 deregulated expression and World Health Organization dysplasia grading to OralCancerPredict in predicting the risk of cancerization and cancer progression–free survival. Moreover, the model had a better net benefit than the World Health Organization and binary dysplasia grading systems alone, which represent the current risk stratification methods in OL management. Overall, OralCancerPredict can predict the risk of cancer development and cancer progression–free survival for patients with OL, with good discrimination, calibration, and net benefit. The explainable artificial intelligence model has the potential to streamline intervention and close monitoring in the clinical management of OL.
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