Machine learning and SHAP value interpretation for predicting the response to neoadjuvant chemotherapy and long-term clinical outcomes in Chinese female breast cancer.

backgroundMost models of neoadjuvant chemotherapy (NACT) for breast cancer (BC) suffer from insufficient data and lack interpretability. Additionally, there is a notable absence of reports from China in this field. This study is also the first to integrate the Advanced Lung Cancer Inflammation Index (ALI) into such a model to evaluate its effectiveness.

methodsData from 3,036 female BC patients receiving NACT at Heilongjiang Provincial Tumor Hospital (2008-2019, median follow-up 7.28 years) were analyzed. After screening, 2,909 patients were randomized into training and validation cohorts (7:3). Using eXtreme Gradient Boosting (XGBoost), Gradient Boosting Classifier (GBC), Support Vector Machine (SVM) models, and SHapley Additive exPlanations (SHAP), the best predicting pathological complete response (pCR) model was identified, and key features were interpreted. The Least Absolute Shrinkage and Selection Operator (LASSO) Cox algorithm, combined with XGBoost and Random Forest (RF) models, identified 9 overlapping prognostic features, enhancing the nomogram's predictive accuracy for overall survival (OS). Kaplan-Meier (KM) analysis revealed varying prognostic outcomes.

resultsThe XGBoost model performed best in predicting pCR, with Area Under Curve (AUC) values of 0.88 and 0.72 in the training and validation sets, respectively. SHAP analysis indicated that ER, HER2 status, ALI, and albumin (Alb) level were the four most important features. The prognostic model was also validated by high AUC values in both training and test sets. KM analysis indicated that lower ALI, non-pCR, and triple-negative BC manifested as worse clinical outcomes. However, the adverse impact of ALI on the prognosis of this cohort was mainly reflected in the long-term recurrence outcomes and non-pCR groups.

conclusionThis study is the first to introduce ALI into the prediction model for BC completing NACT and develop a large-sample model based on XGBoost. Owing to the particularity of the indicators, training and validation were conducted on real clinical data.