ArticleJournal of imaging informatics in medicine2026
Tomosynthesis and Synthesized-2D Breast AI Outputs in a Biopsy-Referred Cohort: A Diagnostic Study of Agreement and Incremental Decision-Support Value.
Article in Journal of imaging informatics in medicine, 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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Abstract
To determine whether two malignancy scores co-reported by a deployed breast artificial intelligence (AI) platform, one tomosynthesis-based and one synthesized-image-based, are interchangeable, and whether either adds information beyond clinical-radiological assessment. This single-center retrospective study analyzed 139 breast-level observations (84 malignant, 55 benign) from 134 biopsy-referred women, with histopathology as reference. Agreement between the two scores was assessed by paired comparison, by whether each output marked a lesion, and by threshold classification. A baseline logistic model (age, radiological suspicion, lesion size) was compared with models adding each score. Cancers negative by the tomosynthesis output at the cohort-derived threshold underwent targeted, AI-masked re-review. The outputs differed within individual breasts despite similar overall discrimination (area under the receiver operating characteristic curve [AUC] 0.728 versus 0.717; p = 0.786). Agreement was moderate (kappa = 0.53); among malignant breasts, 21 were flagged by the tomosynthesis output alone versus 6 by the synthesized output (p = 0.006). Adding either score improved model fit (p < 0.001), but discrimination gains were small (AUC 0.809 to 0.841-0.848) and decision-curve improvements uncertain. Of 30 cancers negative by the tomosynthesis output, 25 had no mammographic correlate on re-review, and breast density did not fully explain this pattern. Within this biopsy-referred cohort, the two AI outputs were not interchangeable. This supports treating co-reported outputs as distinct, context-dependent signals and not using a low AI score by itself to downgrade a suspicious finding. The reporting and governance implications require prospective multireader, multicenter validation.
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