{"title":"A Machine Learning Approach to Prognostication in Oral Cancer: Analysis of the Surveillance, Epidemiology, and End Results Database.","authors":"Philips Okeagu, Saranya Murukutla, Afamdi Iwuchukwu, Chukwuebuka Ogwo","doi":"10.1177/11769351261442875","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To develop and validate machine learning models to predict 5-year survival in oral cancer using a large population-based registry and to rank prognostic factors.</p><p><strong>Methods: </strong>We analyzed Surveillance, Epidemiology, and End Results (SEER) data from 1992 to 2020. After applying inclusion criteria, 39 904 patients with complete data on 21 variables were included from 53 611 cases (25.6% exclusion). Selection bias was assessed by comparing included and excluded patients. The outcome was binary 5-year survival. Four models were trained and evaluated using nested fivefold cross-validation: XGBoost, LASSO, Random Forest, and logistic regression. Performance was assessed using the Brier score, area under the receiver operating characteristic curve (AUC), sensitivity, and specificity. Calibration was evaluated using slope and intercept with 95% confidence intervals. Model explainability used permutation feature importance and SHAP values.</p><p><strong>Results: </strong>Random Forest showed the best discrimination (AUC 77.6%, accuracy 71.4%, Brier 0.186) and was selected for risk stratification. However, it overestimated risk in lower deciles. Logistic regression and LASSO showed better calibration, with slopes near 1.0, but slightly lower discrimination (AUCs 75.5% and 76.9%). SHAP analysis identified localized stage as the strongest protective factor (importance 100.0), followed by age (91.1) and chemotherapy (29.3). Excluded patients had more unstaged tumors (3.9% vs 1.7%, <i>P</i> < .001).</p><p><strong>Conclusion: </strong>Random Forest provides strong risk stratification, but miscalibration limits its use for absolute risk prediction. Logistic regression and LASSO may be preferable when accurate probabilities are needed. External validation is required before clinical use.</p>","PeriodicalId":35418,"journal":{"name":"Cancer Informatics","volume":"25 ","pages":"11769351261442875"},"PeriodicalIF":2.1000,"publicationDate":"2026-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13201935/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer Informatics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/11769351261442875","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MATHEMATICAL & COMPUTATIONAL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To develop and validate machine learning models to predict 5-year survival in oral cancer using a large population-based registry and to rank prognostic factors.
Methods: We analyzed Surveillance, Epidemiology, and End Results (SEER) data from 1992 to 2020. After applying inclusion criteria, 39 904 patients with complete data on 21 variables were included from 53 611 cases (25.6% exclusion). Selection bias was assessed by comparing included and excluded patients. The outcome was binary 5-year survival. Four models were trained and evaluated using nested fivefold cross-validation: XGBoost, LASSO, Random Forest, and logistic regression. Performance was assessed using the Brier score, area under the receiver operating characteristic curve (AUC), sensitivity, and specificity. Calibration was evaluated using slope and intercept with 95% confidence intervals. Model explainability used permutation feature importance and SHAP values.
Results: Random Forest showed the best discrimination (AUC 77.6%, accuracy 71.4%, Brier 0.186) and was selected for risk stratification. However, it overestimated risk in lower deciles. Logistic regression and LASSO showed better calibration, with slopes near 1.0, but slightly lower discrimination (AUCs 75.5% and 76.9%). SHAP analysis identified localized stage as the strongest protective factor (importance 100.0), followed by age (91.1) and chemotherapy (29.3). Excluded patients had more unstaged tumors (3.9% vs 1.7%, P < .001).
Conclusion: Random Forest provides strong risk stratification, but miscalibration limits its use for absolute risk prediction. Logistic regression and LASSO may be preferable when accurate probabilities are needed. External validation is required before clinical use.
期刊介绍:
The field of cancer research relies on advances in many other disciplines, including omics technology, mass spectrometry, radio imaging, computer science, and biostatistics. Cancer Informatics provides open access to peer-reviewed high-quality manuscripts reporting bioinformatics analysis of molecular genetics and/or clinical data pertaining to cancer, emphasizing the use of machine learning, artificial intelligence, statistical algorithms, advanced imaging techniques, data visualization, and high-throughput technologies. As the leading journal dedicated exclusively to the report of the use of computational methods in cancer research and practice, Cancer Informatics leverages methodological improvements in systems biology, genomics, proteomics, metabolomics, and molecular biochemistry into the fields of cancer detection, treatment, classification, risk-prediction, prevention, outcome, and modeling.