Objective: To construct a risk prediction model for delayed chemotherapy-induced nausea and vomiting(CINV) in ovarian cancer patients undergoing chemotherapy based on machine learning algorithms, and to screen the optimal model, so as to provide evidence for clinical individualized prediction, prevention and control. Methods: A total of ovarian cancer patients who received chemotherapy in our hospital from June 2023 to June 2025 were enrolled by convenience sampling. All subjects were randomly divided into the training set and test set at a ratio of 7∶3. General Information Questionnaire, Common Terminology Criteria for Adverse Events(CTCAE 3.0), Self-Rating Anxiety Scale(SAS), Revised Piper Fatigue Scale(RPFS), and Chinese version of Patient Activation Measure(PAM) 13 were adopted for investigation. Participants were divided into the delayed CINV group and non-delayed CINV group according to the occurrence of delayed CINV. LASSO regression was used to screen predictive variables in the training set. Four machine learning models including Logistic regression, support vector machine(SVM), random forest and extreme gradient boosting(XGBoost) were established. Model performance indicators including the area under the curve(AUC), accuracy, precision, recall rate and F1-score were compared to select the optimal model. Results: A total of 409 ovarian cancer patients undergoing chemotherapy were finally included, among whom 192 cases developed delayed CINV, with an incidence rate of 46.94%. In the training set(286 cases), 134 cases had delayed CINV(46.85%); In the test set(123 cases), 58 cases had delayed CINV(47.15%). Eight predictive variables were screened out by LASSO regression: emetogenic risk of chemotherapeutic drugs, history of motion sickness, history of hyperemesis gravidarum, ECOG performance status score, nutritional risk, anxiety, fatigue, and patient activation level. In the training set, the XGBoost model yielded the highest values of AUC, accuracy, precision, recall rate, and F1-score among the four models(0.898, 0.806, 0.825, 0.741, 0.780). In the test set, the AUC of the XGBoost model was 0.861(95%CI: 0.787-0.920), with the highest accuracy, recall rate, and F1-score of 0.765, 0.691, 0.733, respectively. Conclusion: Among the four prediction models, the XGBoost model presents the relatively optimal predictive performance. It can provide a basis for early clinical identification of patients for high risk of delayed CINV and the formulation of individualized preventive and intervention strategies. |
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