Evidence map›Paper›PMID 42014495›Full record

ArticleEuropean radiology2026

From pixels to pathology: how artificial intelligence mammographic risk scores capture tumor biology through imaging.

Zi Zhang, Jafer Elabeid, Thowaiba Ali, Jennifer Pantleo, Nelda Gonzalez, Chirag Parghi

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Article in European radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Zi ZhangLewis Katz School of Medicine at Temple University, Philadelphia, PA, USA. Jill.zi.zhang@gmail.com.ORCID http://orcid.org/0000-0002-3062-3511
Jafer ElabeidFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Thowaiba AliFaculty of Medicine, University of Khartoum, Khartoum, Sudan.
Jennifer PantleoSolis Mammography, Addison, TX, USA.
Nelda GonzalezSolis Mammography, Addison, TX, USA.
Chirag ParghiSolis Mammography, Addison, TX, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo characterize clinical-pathologic tumor features associated with artificial intelligence (AI)-generated risk scores from prior-year screening mammograms. MATERIALS AND

methodsThis retrospective study included women who underwent breast biopsy following a screening mammogram in 2021 across four U.S. states. AI risk scores were obtained from prior-year screening mammograms using an FDA-approved AI model. Receiver operating characteristic (ROC) analysis was used to evaluate the discriminative ability of AI risk scores. Among patients with breast cancer, linear regression was used to assess associations between prior-year risk scores and cancer characteristics.

resultsAmong 1509 patients included (mean age 58.56 ± 12.28 years), 508 (33.7%) had biopsy-confirmed breast cancer. The area under the ROC curve (AUC) for prior-year AI risk score predicting biopsy-confirmed cancer was 0.62 (95% CI: 0.59-0.65). In univariate analysis of biopsy-positive patients, invasive lobular carcinoma (ILC) had significantly higher prior-year AI risk scores than ductal carcinoma in situ (p = 0.009), while Grade 3 tumors had significantly lower scores than Grade 1 (p = 0.016). After adjusting for tumor grade, the ILC association was no longer significant (p = 0.136), suggesting that tumor grade may mediate this relationship; Grade 3 tumors showed a marginal association with lower risk scores (p = 0.068).

conclusionAI-generated risk scores from prior-year screening mammograms demonstrated modest discrimination between biopsy-confirmed malignant and non-malignant cases and may capture imaging features associated with low-grade tumors. Our findings suggest AI risk scores may reflect subtle imaging patterns of low-grade malignancy 1 year before clinical detection, thereby enhancing our understanding of AI model behavior and informing future research on clinical utility. KEY POINTS: Question What clinical-pathologic tumor characteristics are reflected in artificial intelligence (AI)-generated risk scores from prior-year screening mammograms among patients with biopsy-confirmed outcomes? Findings Prior-year AI risk scores demonstrated modest discrimination between biopsy-confirmed malignant and non-malignant cases and may capture imaging features associated with low-grade tumors. Clinical relevance AI-generated risk scores from prior-year screening mammograms may capture subtle imaging features of evolving low-grade malignancy 1 year before clinical detection, offering insights into AI model behavior, enhancing explainability for clinicians, and informing future research on clinical utility.

Indexed as

Artificial IntelligenceBreast NeoplasmsMammographyAgedBiopsyFemaleHumansMiddle AgedNeoplasm GradingRetrospective StudiesRisk AssessmentArtificial intelligenceBreast neoplasmsMammographyRisk assessment

Identifiers

PMID42014495
PMCPMC13341831

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