4.5 Article

Development and validation of machine learning-based risk prediction models of oral squamous cell carcinoma using salivary autoantibody biomarkers

Journal

BMC ORAL HEALTH
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12903-022-02607-2

Keywords

Oral cavity squamous cell carcinoma; Autoantibodies; Biomarker; Machine learning

Funding

  1. Ministry of Science and Technology, Taiwan [MOST 108-2320-B-182-030-MY3]
  2. Chang Gung Memorial Hospital [BMRPC77]

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A machine learning model using salivary autoantibody levels and demographic and behavioral data was successfully established to predict high-risk cases of oral cavity squamous cell carcinoma (OSCC). The model can be applied clinically through an online calculator to provide personalized information and reduce disease morbidity and mortality rates.
Introduction The incidence of oral cavity squamous cell carcinoma (OSCC) continues to rise. OSCC is associated with a low average survival rate, and most patients have a poor disease prognosis because of delayed diagnosis. We used machine learning techniques to predict high-risk cases of OSCC by using salivary autoantibody levels and demographic and behavioral data. Methods We collected the salivary samples of patients recruited from a teaching hospital between September 2008 and December 2012. Ten salivary autoantibodies, sex, age, smoking, alcohol consumption, and betel nut chewing were used to build prediction models for identifying patients with a high risk of OSCC. The machine learning algorithms applied in the study were logistic regression, random forest, support vector machine with the radial basis function kernel, eXtreme Gradient Boosting (XGBoost), and a stacking model. We evaluated the performance of the models by using the area under the receiver operating characteristic curve (AUC), with simulations conducted 100 times. Results A total of 337 participants were enrolled in this study. The best predictive model was constructed using a stacking algorithm with original forms of age and logarithmic levels of autoantibodies (AUC = 0.795 +/- 0.055). Adding autoantibody levels as a data source significantly improved the prediction capability (from 0.698 +/- 0.06 to 0.795 +/- 0.055, p < 0.001). Conclusions We successfully established a prediction model for high-risk cases of OSCC. This model can be applied clinically through an online calculator to provide additional personalized information for OSCC diagnosis, thereby reducing the disease morbidity and mortality rates.

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