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Updated: Sep 14, 2025

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Improving appendix cancer prediction with SHAP-based feature engineering for machine learning models: a prediction

Ji Yoon Kim1

  • 1Ewha Womans University College of Medicine, Seoul, Korea.

Ewha Medical Journal
|July 24, 2025
PubMed
Summary
This summary is machine-generated.

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Shapley additive explanation (SHAP) feature engineering improved appendix cancer prediction accuracy and transparency. This interpretable model enhances clinical relevance for rare disease prediction.

Area of Science:

  • Oncology
  • Artificial Intelligence
  • Machine Learning

Background:

  • Traditional appendix cancer prediction models often lack transparency, limiting clinical adoption.
  • Interpretable AI is crucial for integrating predictive models into clinical practice.

Purpose of the Study:

  • To develop and evaluate a Shapley additive explanation (SHAP)-based feature engineering framework for appendix cancer prediction.
  • To enhance model accuracy and clinical interpretability by integrating SHAP for feature selection, construction, and weighting.

Main Methods:

  • Utilized the Kaggle Appendix Cancer Prediction dataset (260,000 samples, 21 features).
  • Applied data preprocessing including label encoding and SMOTE for class imbalance.
  • Compared baseline models (Random Forest, XGBoost, LightGBM), selecting LightGBM for superior performance.
Keywords:
AlgorithmsAppendiceal neoplasmsMachine learningRandom forest

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  • Implemented SHAP analysis for feature selection, interaction-based feature construction, and feature weighting.
  • Main Results:

    • The SHAP-based framework improved LightGBM model performance, with feature weighting achieving the highest F1-score (0.8877) and precision (0.9940).
    • Key predictive features identified included red blood cell count and chronic severity.
    • The engineered models maintained interpretability while enhancing predictive accuracy.

    Conclusions:

    • The SHAP-based feature engineering framework significantly improved appendix cancer prediction accuracy and transparency.
    • This approach offers a scalable and interpretable solution for rare disease prediction.
    • Further validation with real-world data is recommended to ensure generalizability.