Evidence map›Paper›PMID 40249223›Full record

ArticleJournal of the National Cancer Institute2025

Mammographic classification of interval breast cancers and artificial intelligence performance.

Tiffany T Yu, Anne C Hoyt, Melissa M Joines, Cheryce P Fischer, Nazanin Yaghmai, James S Chalfant, Lucy Chow, Shabnam Mortazavi, Christopher D Sears, James Sayre and 3 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
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  4. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Tiffany T YuDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.ORCID 0000-0002-8722-2700
Anne C HoytDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.ORCID 0000-0002-3927-5349
Melissa M JoinesDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.
Cheryce P FischerDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.
Nazanin YaghmaiDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.
James S ChalfantDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.ORCID 0000-0001-6385-604X
Lucy ChowDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.ORCID 0000-0003-4084-442X
Shabnam MortazaviDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.
Christopher D SearsDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.ORCID 0009-0002-4446-5486
James SayreDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.ORCID 0000-0001-6090-8713
Joann G ElmoreDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.ORCID 0000-0002-7311-6835
William HsuDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.ORCID 0000-0002-5168-070X
Hannah S MilchDavid Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, United States.

Funding

Artificial Intelligence for Improved Breast Cancer Screening Accuracy: External Validation, Refinement, and Clinical TranslationR37CA240403 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI CHRISTOPH I LEE · 2020 to 2026
$3.8M
AHRQ HHS R21 HS029257AHRQ HHS R33 HS029257Early Diagnostics IncNCI NIH HHS R37 CA240403NIH HHS
6 · The paper itself

Abstract

backgroundEuropean studies suggest that artificial intelligence (AI) can reduce interval breast cancers. Research on interval breast cancer classification and AI's effectiveness in the United States, however, particularly using digital breast tomosynthesis and annual screening, is limited. We aimed to mammographically classify interval breast cancers and assess AI performance using a 12-month screening interval.

methodsFrom digital mammography and digital breast tomosynthesis screening mammograms acquired between 2010 and 2019 at a US tertiary-care academic center, we identified interval breast cancers diagnosed less than 12 months after a negative mammogram. At least 3 breast radiologists retrospectively classified interval breast cancers as missed-reading error, minimal signs-actionable, minimal signs-nonactionable, true interval, occult, or missed-technical error. A deep-learning AI tool assigned risk scores ranging from 1 to 10 to the negative index screening mammograms, with scores of 8 or higher considered "flagged." Statistical analysis evaluated associations among interval breast cancer types and AI exam scores, AI markings, and patient and tumor characteristics.

resultsFrom 184 935 screening mammograms (65% digital mammography, 35% digital breast tomosynthesis), we identified 148 interval breast cancers in 148 women (mean [SD] age = 61 [12] years). Of these, 26% were minimal signs-actionable, 24% were occult, 22% were minimal signs-nonactionable, 17% were missed-reading error, 6% were true interval, and 5% were missed-technical error (P < .001). AI scored 131 mammograms (17 errors excluded); it most frequently flagged exams with missed-reading error (90%), minimal signs-actionable (89%), and minimal signs-nonactionable (72%) (P = .02). AI localized mammographically visible types more accurately (35%-68%) than nonvisible types (0%-50%; P = .02).

conclusionAI more frequently flagged and accurately localized interval breast cancer types that were mammographically visible at screening (missed or minimal signs) compared with true interval or occult cancers.

Indexed as

Artificial IntelligenceBreast NeoplasmsEarly Detection of CancerMammographyAgedFemaleHumansMiddle AgedRetrospective Studies

Identifiers

PMID40249223
PMCPMC12342771

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.