Evidence map›Paper›PMID 38528136›Full record

ArticleEuropean radiology2024

AI performance by mammographic density in a retrospective cohort study of 99,489 participants in BreastScreen Norway.

Marie Burns Bergan, Marthe Larsen, Nataliia Moshina, Hauke Bartsch, Henrik Wethe Koch, Hildegunn Siv Aase, Zhanbolat Satybaldinov, Ingfrid Helene Salvesen Haldorsen, Christoph I Lee, Solveig Hofvind

Open access · hybridAbstract read
In one paragraph

Article in European radiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.8field-weighted citation impact, top 7% of its field
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

9 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Marie Burns BerganSection for Breast Cancer Screening, Cancer Registry of Norway, Norwegian Institute of Public Health, P.O. Box 5313, 0304, Oslo, Norway.
Marthe LarsenSection for Breast Cancer Screening, Cancer Registry of Norway, Norwegian Institute of Public Health, P.O. Box 5313, 0304, Oslo, Norway.
Nataliia MoshinaSection for Breast Cancer Screening, Cancer Registry of Norway, Norwegian Institute of Public Health, P.O. Box 5313, 0304, Oslo, Norway.
Hauke BartschDepartment of Radiology, Mohn Medical Imaging and Visualization Centre (MMIV), Haukeland University Hospital, Bergen, Norway.
Henrik Wethe KochDepartment of Radiology, Stavanger University Hospital, Stavanger, Norway.
Hildegunn Siv AaseDepartment of Radiology, Haukeland University Hospital, Bergen, Norway.
Zhanbolat SatybaldinovDepartment of Radiology, Mohn Medical Imaging and Visualization Centre (MMIV), Haukeland University Hospital, Bergen, Norway.
Ingfrid Helene Salvesen HaldorsenDepartment of Radiology, Mohn Medical Imaging and Visualization Centre (MMIV), Haukeland University Hospital, Bergen, Norway.
Christoph I LeeDepartment of Radiology, University of Washington School of Medicine, Seattle, WA, USA.
Solveig HofvindSection for Breast Cancer Screening, Cancer Registry of Norway, Norwegian Institute of Public Health, P.O. Box 5313, 0304, Oslo, Norway. sshh@kreftregisteret.no.ORCID http://orcid.org/0000-0003-0178-8939
Haukeland University Hospital · NONorwegian Institute of Public Health · NOCancer Registry of Norway · NOStavanger University Hospital · NOUniversity of Washington · US

Funding

Kreftforeningen 214931
6 · The paper itself

Abstract

objectiveTo explore the ability of artificial intelligence (AI) to classify breast cancer by mammographic density in an organized screening program. MATERIALS AND

methodWe included information about 99,489 examinations from 74,941 women who participated in BreastScreen Norway, 2013-2019. All examinations were analyzed with an AI system that assigned a malignancy risk score (AI score) from 1 (lowest) to 10 (highest) for each examination. Mammographic density was classified into Volpara density grade (VDG), VDG1-4; VDG1 indicated fatty and VDG4 extremely dense breasts. Screen-detected and interval cancers with an AI score of 1-10 were stratified by VDG.

resultsWe found 10,406 (10.5% of the total) examinations to have an AI risk score of 10, of which 6.7% (704/10,406) was breast cancer. The cancers represented 89.7% (617/688) of the screen-detected and 44.6% (87/195) of the interval cancers. 20.3% (20,178/99,489) of the examinations were classified as VDG1 and 6.1% (6047/99,489) as VDG4. For screen-detected cancers, 84.0% (68/81, 95% CI, 74.1-91.2) had an AI score of 10 for VDG1, 88.9% (328/369, 95% CI, 85.2-91.9) for VDG2, 92.5% (185/200, 95% CI, 87.9-95.7) for VDG3, and 94.7% (36/38, 95% CI, 82.3-99.4) for VDG4. For interval cancers, the percentages with an AI score of 10 were 33.3% (3/9, 95% CI, 7.5-70.1) for VDG1 and 48.0% (12/25, 95% CI, 27.8-68.7) for VDG4.

conclusionThe tested AI system performed well according to cancer detection across all density categories, especially for extremely dense breasts. The highest proportion of screen-detected cancers with an AI score of 10 was observed for women classified as VDG4. CLINICAL RELEVANCE STATEMENT: Our study demonstrates that AI can correctly classify the majority of screen-detected and about half of the interval breast cancers, regardless of breast density. KEY POINTS: • Mammographic density is important to consider in the evaluation of artificial intelligence in mammographic screening. • Given a threshold representing about 10% of those with the highest malignancy risk score by an AI system, we found an increasing percentage of cancers with increasing mammographic density. • Artificial intelligence risk score and mammographic density combined may help triage examinations to reduce workload for radiologists.

Indexed as

Artificial IntelligenceBreast DensityBreast NeoplasmsMammographyAdultAgedBreastEarly Detection of CancerFemaleHumansMass ScreeningMiddle AgedNorwayRetrospective StudiesArtificial intelligenceBreast cancerBreast densityMammographyScreening

Identifiers

PMID38528136
PMCPMC11399294
OpenAlexW4393162877

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.