Evidence map›Paper›PMID 38395930›Full record

ArticleBreast cancer research : BCR2024

Augmented interpretation of HER2, ER, and PR in breast cancer by artificial intelligence analyzer: enhancing interobserver agreement through a reader study of 201 cases.

Minsun Jung, Seung Geun Song, Soo Ick Cho, Sangwon Shin, Taebum Lee, Wonkyung Jung, Hajin Lee, Jiyoung Park, Sanghoon Song, Gahee Park and 10 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
9.7field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 28 citations in OpenAlex.

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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

20 authors at 3 institutions in 1 country.

Minsun Jung *Department of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Seung Geun Song *Department of Pathology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Soo Ick ChoLunit, Seoul, Republic of Korea.
Sangwon ShinLunit, Seoul, Republic of Korea.
Taebum LeeLunit, Seoul, Republic of Korea.
Wonkyung JungLunit, Seoul, Republic of Korea.
Hajin LeeLunit, Seoul, Republic of Korea.
Jiyoung ParkLunit, Seoul, Republic of Korea.
Sanghoon SongLunit, Seoul, Republic of Korea.
Gahee ParkLunit, Seoul, Republic of Korea.
Heon SongLunit, Seoul, Republic of Korea.
Seonwook ParkLunit, Seoul, Republic of Korea.
Jinhee LeeLunit, Seoul, Republic of Korea.
Mingu KangLunit, Seoul, Republic of Korea.
Jongchan ParkLunit, Seoul, Republic of Korea.
Sergio PereiraLunit, Seoul, Republic of Korea.
Donggeun YooLunit, Seoul, Republic of Korea.
Keunhyung ChungLunit, Seoul, Republic of Korea.
Siraj M AliLunit, Seoul, Republic of Korea.
So-Woon KimDepartment of Pathology, Kyung Hee University Hospital, Kyung Hee University College of Medicine, Seoul, Republic of Korea. swkdek@gmail.com.
Seoul National University · KRKyung Hee University · KRYonsei University · KR

Funding

National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) NRF-2022R1A2C1010536
6 · The paper itself

Abstract

backgroundAccurate classification of breast cancer molecular subtypes is crucial in determining treatment strategies and predicting clinical outcomes. This classification largely depends on the assessment of human epidermal growth factor receptor 2 (HER2), estrogen receptor (ER), and progesterone receptor (PR) status. However, variability in interpretation among pathologists pose challenges to the accuracy of this classification. This study evaluates the role of artificial intelligence (AI) in enhancing the consistency of these evaluations.

methodsAI-powered HER2 and ER/PR analyzers, consisting of cell and tissue models, were developed using 1,259 HER2, 744 ER, and 466 PR-stained immunohistochemistry (IHC) whole-slide images of breast cancer. External validation cohort comprising HER2, ER, and PR IHCs of 201 breast cancer cases were analyzed with these AI-powered analyzers. Three board-certified pathologists independently assessed these cases without AI annotation. Then, cases with differing interpretations between pathologists and the AI analyzer were revisited with AI assistance, focusing on evaluating the influence of AI assistance on the concordance among pathologists during the revised evaluation compared to the initial assessment.

resultsReevaluation was required in 61 (30.3%), 42 (20.9%), and 80 (39.8%) of HER2, in 15 (7.5%), 17 (8.5%), and 11 (5.5%) of ER, and in 26 (12.9%), 24 (11.9%), and 28 (13.9%) of PR evaluations by the pathologists, respectively. Compared to initial interpretations, the assistance of AI led to a notable increase in the agreement among three pathologists on the status of HER2 (from 49.3 to 74.1%, p < 0.001), ER (from 93.0 to 96.5%, p = 0.096), and PR (from 84.6 to 91.5%, p = 0.006). This improvement was especially evident in cases of HER2 2+ and 1+, where the concordance significantly increased from 46.2 to 68.4% and from 26.5 to 70.7%, respectively. Consequently, a refinement in the classification of breast cancer molecular subtypes (from 58.2 to 78.6%, p < 0.001) was achieved with AI assistance.

conclusionsThis study underscores the significant role of AI analyzers in improving pathologists' concordance in the classification of breast cancer molecular subtypes.

Indexed as

Breast NeoplasmsArtificial IntelligenceBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesFemaleHumansObserver VariationReceptors, EstrogenReceptors, ProgesteroneBiomarkers, TumorErb-b2 Receptor Tyrosine KinasesReceptors, EstrogenReceptors, ProgesteroneArtificial intelligence (AI)Breast cancerConcordanceDigital pathologyEstrogen receptor (ER)Human epidermal growth factor receptor 2 (HER2)Progesterone receptor (PR)Whole-slide image (WSI)

Identifiers

PMID38395930
PMCPMC10885430
OpenAlexW4392103977

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.