Development and validation of interpretable machine learning model for pre-treatment predicting the response to targeted and immune therapy in hepatocellular carcinoma.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
413 patients from two institutions who received targeted and immune therapy.
I · Intervention 중재 / 시술
targeted and immune therapy
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Kaplan-Meier analysis showed that high-risk scores stratified by XGBoost model were associated with shorter OS (HR: 0.740, 95 % CI: 0.665-0.823, P < 0.001). [CONCLUSION] XGBoost model effectively predicted treatment response and prognosis in HCC patients undergoing targeted and immune therapy, offering a noninvasive tool to guide treatment decisions and optimize clinical outcomes.
[BACKGROUND] Targeted and immune therapies are used for unresectable hepatocellular carcinoma (HCC), but their efficacy is limited by tumor heterogeneity.
- p-value P < 0.001
- 95% CI 0.744-0.860
- HR 0.740
APA
Huang R, Liu K, et al. (2025). Development and validation of interpretable machine learning model for pre-treatment predicting the response to targeted and immune therapy in hepatocellular carcinoma.. European journal of radiology, 191, 112353. https://doi.org/10.1016/j.ejrad.2025.112353
MLA
Huang R, et al.. "Development and validation of interpretable machine learning model for pre-treatment predicting the response to targeted and immune therapy in hepatocellular carcinoma.." European journal of radiology, vol. 191, 2025, pp. 112353.
PMID
40818216
Abstract
[BACKGROUND] Targeted and immune therapies are used for unresectable hepatocellular carcinoma (HCC), but their efficacy is limited by tumor heterogeneity. Identifying patients who will benefit from targeted and immune therapy is crucial for optimizing treatment strategies and prognosis. We aimed to develop and validate interpretable machine learning (ML) models integrating clinical and CT imaging characteristics for pretreatment prediction of objective response and prognosis to targeted and immune therapy in HCC.
[METHODS] This retrospective multicenter study included 413 patients from two institutions who received targeted and immune therapy. Clinical and CT characteristics were collected. Logistic Regression (LR), Support Vector Machine (SVM), Random Forest (RF), and eXtreme Gradient Boosting (XGBoost) models were developed and validated to predict treatment response and overall survival (OS). Model performance was assessed by area under the curve (AUC) and Kaplan-Meier analysis. Additionally, SHAP (SHapley Additive exPlanations) analysis explained model predictions by aggregating the attribution values for each input feature.
[RESULTS] The XGBoost model demonstrated the best performance with AUCs of 0.802 (95 % CI: 0.744-0.860) and 0.805 (95 % CI: 0.741-0.868) in training and validation cohorts. Significant predictors included Barcelona Clinic Liver Cancer (BCLC) stage, tumor number, tumor margin, peritumoral enhancement and macrovascular invasion. Kaplan-Meier analysis showed that high-risk scores stratified by XGBoost model were associated with shorter OS (HR: 0.740, 95 % CI: 0.665-0.823, P < 0.001).
[CONCLUSION] XGBoost model effectively predicted treatment response and prognosis in HCC patients undergoing targeted and immune therapy, offering a noninvasive tool to guide treatment decisions and optimize clinical outcomes.
[METHODS] This retrospective multicenter study included 413 patients from two institutions who received targeted and immune therapy. Clinical and CT characteristics were collected. Logistic Regression (LR), Support Vector Machine (SVM), Random Forest (RF), and eXtreme Gradient Boosting (XGBoost) models were developed and validated to predict treatment response and overall survival (OS). Model performance was assessed by area under the curve (AUC) and Kaplan-Meier analysis. Additionally, SHAP (SHapley Additive exPlanations) analysis explained model predictions by aggregating the attribution values for each input feature.
[RESULTS] The XGBoost model demonstrated the best performance with AUCs of 0.802 (95 % CI: 0.744-0.860) and 0.805 (95 % CI: 0.741-0.868) in training and validation cohorts. Significant predictors included Barcelona Clinic Liver Cancer (BCLC) stage, tumor number, tumor margin, peritumoral enhancement and macrovascular invasion. Kaplan-Meier analysis showed that high-risk scores stratified by XGBoost model were associated with shorter OS (HR: 0.740, 95 % CI: 0.665-0.823, P < 0.001).
[CONCLUSION] XGBoost model effectively predicted treatment response and prognosis in HCC patients undergoing targeted and immune therapy, offering a noninvasive tool to guide treatment decisions and optimize clinical outcomes.
🏷️ 키워드 / MeSH
- Humans
- Carcinoma
- Hepatocellular
- Liver Neoplasms
- Male
- Female
- Retrospective Studies
- Machine Learning
- Middle Aged
- Tomography
- X-Ray Computed
- Aged
- Immunotherapy
- Treatment Outcome
- Prognosis
- Reproducibility of Results
- Adult
- Hepatocellular carcinoma
- Immune therapy
- Machine learning
- Prognosis prediction
- Targeted therapy
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