Identifying Data-Driven Clinical Subgroups for Cervical Cancer Prevention With Machine Learning: Population-Based, External, and Diagnostic Validation Study

cervical cancer
human papillomavirus
screening
machine learning
cervical tumor
cancer
carcinoma
tumor
malignant
ml
phenomapping strategy
logistic regression
regression
population-based
validation study
cancer prevention
validity
usability
algorithm
surveillance
electronic health record
ehr

Lu Z, Dong B, Cai H, et al. Identifying Data-Driven Clinical Subgroups for Cervical Cancer Prevention With Machine Learning: Population-Based, External, and Diagnostic Validation Study. JMIR Public Health Surveill 2025; 11: e67840.

Author
Affiliation

School of Public Health (Shenzhen), Sun Yat-sen University

Published

March 2025

Doi

Abstract

BACKGROUND: Cervical cancer remains a major global health issue. Personalized, data-driven cervical cancer prevention (CCP) strategies tailored to phenotypic profiles may improve prevention and reduce disease burden. OBJECTIVE: This study aimed to identify subgroups with differential cervical precancer or cancer risks using machine learning, validate subgroup predictions across datasets, and propose a computational phenomapping strategy to enhance global CCP efforts. METHODS: We explored the data-driven CCP subgroups by applying unsupervised machine learning to a deeply phenotyped, population-based discovery cohort. We extracted CCP-specific risks of cervical intraepithelial neoplasia (CIN) and cervical cancer through weighted logistic regression analyses providing odds ratio (OR) estimates and 95% CIs. We trained a supervised machine learning model and developed pathways to classify individuals before evaluating its diagnostic validity and usability on an external cohort. RESULTS: This study included 551,934 women (median age, 49 years) in the discovery cohort and 47,130 women (median age, 37 years) in the external cohort. Phenotyping identified 5 CCP subgroups, with CCP4 showing the highest carcinoma prevalence. CCP2-4 had significantly higher risks of CIN2+ (CCP2: OR 2.07 [95% CI: 2.03-2.12], CCP3: 3.88 [3.78-3.97], and CCP4: 4.47 [4.33-4.63]) and CIN3+ (CCP2: 2.10 [2.05-2.14], CCP3: 3.92 [3.82-4.02], and CCP4: 4.45 [4.31-4.61]) compared to CCP1 (P<.001), consistent with the direction of results observed in the external cohort. The proposed triple strategy was validated as clinically relevant, prioritizing high-risk subgroups (CCP3-4) for colposcopies and scaling human papillomavirus screening for CCP1-2. CONCLUSIONS: This study underscores the potential of leveraging machine learning algorithms and large-scale routine electronic health records to enhance CCP strategies. By identifying key determinants of CIN2+/CIN3+ risk and classifying 5 distinct subgroups, our study provides a robust, data-driven foundation for the proposed triple strategy. This approach prioritizes tailored prevention efforts for subgroups with varying risks, offering a novel and scalable tool to complement existing cervical cancer screening guidelines. Future work should focus on independent external and prospective validation to maximize the global impact of this strategy.

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@article{RN1179,
   author = {Lu, Z. and Dong, B. and Cai, H. and Tian, T. and Wang, J. and Fu, L. and Wang, B. and Zhang, W. and Lin, S. and Tuo, X. and Wang, J. and Yang, T. and Huang, X. and Zheng, Z. and Xue, H. and Xu, S. and Liu, S. and Sun, P. and Zou, H.},
   title = {Identifying Data-Driven Clinical Subgroups for Cervical Cancer Prevention With Machine Learning: Population-Based, External, and Diagnostic Validation Study},
   journal = {JMIR Public Health Surveill},
   volume = {11},
   pages = {e67840},
   ISSN = {2369-2960 (Electronic)
2369-2960 (Linking)},
   DOI = {10.2196/67840},
   url = {https://www.ncbi.nlm.nih.gov/pubmed/40106366},
   year = {2025},
   type = {Journal Article}
}