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Accepted for/Published in: JMIR Cancer

Date Submitted: Jun 2, 2024
Date Accepted: Mar 20, 2025

The final, peer-reviewed published version of this preprint can be found here:

Association Between Risk Factors and Major Cancers: Explainable Machine Learning Approach

Huang X, Ren S, Mao X, Chen S, Chen E, He Y, Jiang Y

Association Between Risk Factors and Major Cancers: Explainable Machine Learning Approach

JMIR Cancer 2025;11:e62833

DOI: 10.2196/62833

PMID: 40315870

PMCID: 12064211

Leveraging Explainable Machine Learning to Uncover the Association between Risk Factors and Major Cancers: Cancer Risk Factor Association Study

  • Xiayuan Huang; 
  • ShuShun Ren; 
  • Xinyue Mao; 
  • Serena Chen; 
  • Elle Chen; 
  • Yuqi He; 
  • Yun Jiang

ABSTRACT

Background:

Cancer is a life-threatening disease and a leading cause of death worldwide, with an estimated 611,000 deaths and over 2 million new cases in the United States in 2024. The rising incidence of major cancers, including among younger individuals, highlights the need for early screening and monitoring of risk factors to manage and decrease cancer risk.

Objective:

This study aimed to leverage explainable machine learning models to identify and analyze the key risk factors associated with breast, colorectal, lung, and prostate cancers. By uncovering significant associations between risk factors and these major cancer types, we sought to enhance the understanding of cancer risk profiles. Our goal was to facilitate more precise screening, early detection, and personalized prevention strategies, ultimately contributing to better patient outcomes and promoting health equity.

Methods:

De-identified electronic health record data from MIMIC-III was used to identify patients with four types of cancer who had longitudinal hospital visits prior to their diagnosis presence. Their records were matched and combined with those of patients without cancer diagnoses using propensity scores based on demographic factors. Three advanced models, penalized Logistic Regression (LR), Random Forest (RF), and Multilayer Perceptron (MLP), were conducted to identify the rank of risk factors for each cancer type, with feature importance analysis for RF and MLP models. The Rank Biased Overlap was adopted to compare the similarity of ranked risk factors across cancer types.

Results:

Our framework evaluated the prediction performance of explainable machine learning models, with MLP model demonstrating the best performance. It achieved an AUC of 0.78 for breast cancer (N=58), 0.76 for colorectal cancer (N=140), 0.84 for lung cancer (N=398), and 0.78 for prostate cancer (N=104), outperforming other baseline models (P-value<0.01). In addition to demographic risk factors, the most prominent non-traditional risk factors overlapped across models and cancer types, including hyperlipidemia (OR=1.14, 95% CI: 1.11-1.17, P-value<0.01), diabetes (OR=1.34, 95% CI: 1.29-1.39, P-value<0.01), depressive disorders (OR=1.11, 95% CI: 1.06-1.16, P-value<0.01), heart diseases (OR=1.42, 95% CI: 1.32-1.52, P-value<0.01), and anemia (OR=1.22, 95% CI: 1.14-1.30, P-value<0.01). The similarity analysis indicated the unique risk factor pattern for lung cancer from other cancer types.

Conclusions:

The study’s findings demonstrated the effectiveness of explainable ML models in assessing non-traditional risk factors for major cancers and highlighted the importance of considering unique risk profiles for different cancer types. Moreover, this research served as a hypothesis-generating foundation, providing preliminary results for future investigation into cancer risk analysis and management. Furthermore, expanding collaboration with clinical experts for external validation would be essential to refine model outputs, integrate findings into practice, and enhance their impact on patient care and cancer prevention efforts.


 Citation

Please cite as:

Huang X, Ren S, Mao X, Chen S, Chen E, He Y, Jiang Y

Association Between Risk Factors and Major Cancers: Explainable Machine Learning Approach

JMIR Cancer 2025;11:e62833

DOI: 10.2196/62833

PMID: 40315870

PMCID: 12064211

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