Evidence map›Paper›PMID 37847456›Full record

ArticleBreast cancer research and treatment2024

Evaluation of the international Ki67 working group cut point recommendations for early breast cancer: comparison with 21-gene assay results in a large integrated health care system.

Veronica C Shim, Robin J Baker, Wen Jing, Roisin Puentes, Sally S Agersborg, Thomas K Lee, Wamda GoreaI, Ninah Achacoso, Catherine Lee, Marvella Villasenor and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

3 citing papers in PubMed, 5 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

13 authors at 2 institutions in 1 country.

Veronica C ShimThe Permanente Medical Group, Northern California Kaiser Permanente, Oakland, CA, USA.
Robin J BakerThe Permanente Medical Group, Northern California Kaiser Permanente, San Francisco, CA, USA.
Wen JingThe Permanente Medicine, Northern California Kaiser Permanente, San Francisco, CA, USA.
Roisin PuentesNeoGenomics Laboratories, Inc., Aliso Viejo, CA, USA.
Sally S AgersborgNeoGenomics Laboratories, Inc., Aliso Viejo, CA, USA.
Thomas K LeeNeoGenomics Laboratories, Inc., Aliso Viejo, CA, USA.
Wamda GoreaINeoGenomics Laboratories, Inc., Aliso Viejo, CA, USA.
Ninah AchacosoThe Division of Research, Northern California Kaiser Permanente, 2000 Broadway, Oakland, CA, 94612, USA.
Catherine LeeThe Division of Research, Northern California Kaiser Permanente, 2000 Broadway, Oakland, CA, 94612, USA.
Marvella VillasenorThe Division of Research, Northern California Kaiser Permanente, 2000 Broadway, Oakland, CA, 94612, USA.
Amy LinThe Permanente Medical Group, Northern California Kaiser Permanente, San Francisco, CA, USA.
Malathy KapaliThe Permanente Medical Group, Northern California Kaiser Permanente, Sacramento, CA, USA.
Laurel A HabelThe Division of Research, Northern California Kaiser Permanente, 2000 Broadway, Oakland, CA, 94612, USA. laurel.habel@kp.org.ORCID http://orcid.org/0000-0002-7230-587X
Kaiser Permanente · USNeoGenomics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe International Ki67 Working Group (IKWG) has developed training for immunohistochemistry (IHC) scoring reproducibility and recommends cut points of ≤ 5% and ≥ 30% for prognosis in ER+, HER2-, stage I/II breast cancer. We examined scoring reproducibility following IKWG training and evaluated these cut points for selecting patients for further testing with the 21-gene Recurrence Score (RS) assay.

methodsWe included 307 women aged 50+ years with node-negative, ER+PR+HER2- breast cancer and with available RS results. Slides from the diagnostic biopsy were stained for Ki67 and scored using digital image analysis (IA). Two IHC pathologists underwent IKWG training and visually scored slides, blinded to each other and IA readings. Interobserver reproducibility was examined using intraclass correlation (ICC) and Kappa statistics.

resultsDepending on reader, 8.8-16.0% of our cohort had Ki67 ≤ 5% and 11.4-22.5% had scores ≥ 30%. The ICC for Ki67 scores by the two pathologists was 0.82 (95% CI 0.78-0.85); it was 0.79 (95% CI 0.74-0.83) for pathologist 1 and IA and 0.76 (95% CI 0.71-0.80) for pathologist 2 and IA. For Ki67 scores ≤ 5%, the percentages with RS < 26 were 92.6%, 91.8%, and 90.9% for pathologist 1, pathologist 2, and IA, respectively. For Ki67 scores ≥ 30%, the percentages with RS ≥ 26 were 41.5%, 51.4%, and 27.5%, respectively.

conclusionThe IKWG's Ki67 training resulted in moderate to strong reproducibility across readers but cut points had only moderate overlap with RS cut points, especially for Ki67 ≥ 30% and RS ≥ 26; thus, their clinical utility for a 21-gene assay testing pathway remains unclear.

Indexed as

Breast NeoplasmsBiomarkers, TumorFemaleHumansImmunohistochemistryKi-67 AntigenPrognosisReproducibility of ResultsBiomarkers, TumorKi-67 AntigenBreast cancerImmunohistochemistryKi67PrognosisReproducibility

Identifiers

PMID37847456
PMCPMC10787679
OpenAlexW4387692679

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.