Fairness Evaluation of Risk Estimation Models for Lung Cancer Screening

Lung cancer is the leading cause of cancer-related mortality in adults worldwide. Screening high-risk individuals with annual low-dose CT (LDCT) can support earlier detection and reduce deaths, but widespread implementation may strain the already limited radiology workforce. Artificial intelligence (AI) models have shown potential in estimating lung cancer risk from LDCT scans. However, high-risk populations for lung cancer are diverse, and these models’ performance across diverse demographic groups remains an open question. In this study, we used the JustEFAB ethical framework to evaluate potential performance disparities and fairness in two AI-based risk estimation models for lung cancer screening: the Sybil lung cancer risk model and the Venkadesh21 nodule risk estimator. We also examined disparities in the PanCan2b logistic regression model recommended in the British Thoracic Society nodule management guideline. Both AI-based models were trained on data from the U.S.-based National Lung Screening Trial (NLST), and assessed on a held-out NLST validation set. We evaluated area under the ROC curve (AUROC), sensitivity, and specificity across demographic subgroups, and explored potential confounding from clinical risk factors. We observed a statistically significant AUROC difference in Sybil’s performance between women (0.88, 95% CI: 0.86, 0.90) and men (0.81, 95% CI: 0.78, 0.84, p < .001). At 90% specificity, Venkadesh21 showed lower sensitivity for Black (0.39, 95% CI: 0.23, 0.59) than White participants (0.69, 95% CI: 0.65, 0.73). These differences were not explained by available clinical confounders and may be classified as unfair biases according to JustEFAB. Our findings highlight the importance of improving and monitoring model performance across underrepresented subgroups in lung cancer screening, as well as further research on algorithmic fairness in this field.

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Publication Details

Journal
The Journal of Machine Learning for Biomedical Imaging
Published
2025-12-21
DOI
https://doi.org/10.59275/j.melba.2025-1e7f
Primary Topic
Lung Cancer Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Fairness Evaluation of Risk Estimation Models for Lung Cancer Screening

Colin Jacobs, Fennie Van der Graaf, Michel G. Vitale, Shaurya Gaur et al.
The Journal of Machine Learning for Biomedical Imaging
Lung Cancer Diagnosis and Treatment
article

Fairness Evaluation of Risk Estimation Models for Lung Cancer Screening

Colin Jacobs, Fennie Van der Graaf, Michel G. Vitale, Shaurya Gaur, Alessa Hering, Lena Philipp, Johan Kwisthout
article en

Abstract

Lung cancer is the leading cause of cancer-related mortality in adults worldwide. Screening high-risk individuals with annual low-dose CT (LDCT) can support earlier detection and reduce deaths, but widespread implementation may strain the already limited radiology workforce. Artificial intelligence (AI) models have shown potential in estimating lung cancer risk from LDCT scans. However, high-risk populations for lung cancer are diverse, and these models’ performance across diverse demographic groups remains an open question. In this study, we used the JustEFAB ethical framework to evaluate potential performance disparities and fairness in two AI-based risk estimation models for lung cancer screening: the Sybil lung cancer risk model and the Venkadesh21 nodule risk estimator. We also examined disparities in the PanCan2b logistic regression model recommended in the British Thoracic Society nodule management guideline. Both AI-based models were trained on data from the U.S.-based National Lung Screening Trial (NLST), and assessed on a held-out NLST validation set. We evaluated area under the ROC curve (AUROC), sensitivity, and specificity across demographic subgroups, and explored potential confounding from clinical risk factors. We observed a statistically significant AUROC difference in Sybil’s performance between women (0.88, 95% CI: 0.86, 0.90) and men (0.81, 95% CI: 0.78, 0.84, p < .001). At 90% specificity, Venkadesh21 showed lower sensitivity for Black (0.39, 95% CI: 0.23, 0.59) than White participants (0.69, 95% CI: 0.65, 0.73). These differences were not explained by available clinical confounders and may be classified as unfair biases according to JustEFAB. Our findings highlight the importance of improving and monitoring model performance across underrepresented subgroups in lung cancer screening, as well as further research on algorithmic fairness in this field.

The Journal of Machine Learning for Biomedical ImagingVol. 3(Special on FAIMI)
Radboud University Nijmegen (NL), Radboud University Medical Center (NL)
Siemens Healthineers
Good health and well-being
Openalex Percentile: Top 29%
Lung Cancer Diagnosis and Treatment
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