Faculty, Staff and Student Publications

Language

English

Publication Date

4-29-2025

Journal

Bioengineering

DOI

10.3390/bioengineering12050472

PMID

40428091

PMCID

PMC12108849

PubMedCentral® Posted Date

4-29-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Background: Cancer is a leading cause of death worldwide, and its early detection is crucial for improving patient outcomes. This study aimed to develop and evaluate ensemble learning models, specifically stacking, for the accurate prediction of lung, breast, and cervical cancers using lifestyle and clinical data.

Methods: 12 base learners were trained on datasets for lung, breast, and cervical cancer. Stacking ensemble models were then developed using these base learners. The models were evaluated for accuracy, precision, recall, F1-score, AUC-ROC, MCC, and kappa. An explainable AI technique, SHAP, was used to interpret model predictions.

Results: The stacking ensemble model outperformed individual base learners across all three cancer types. On average, for three cancer datasets, it achieved 99.28% accuracy, 99.55% precision, 97.56% recall, and 98.49% F1-score. A similar high performance was observed in terms of AUC, Kappa, and MCC. The SHAP analysis revealed the most influential features for each cancer type, e.g., fatigue and alcohol consumption for lung cancer, worst concave points, mean concave points, and worst perimeter for breast cancer and Schiller test for cervical cancer.

Conclusions: The stacking-based multi-cancer prediction model demonstrated superior accuracy and interpretability compared with traditional models. Combining diverse base learners with explainable AI offers predictive power and transparency in clinical applications. Key demographic and clinical features driving cancer risk were also identified. Further research should validate the model on more diverse populations and cancer types.

Keywords

cancer prediction, ensemble learning, stacking, lung cancer, breast cancer, cervical cancer, XAI, SHAP

Published Open-Access

yes

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