Evidence map›Paper›PMID 40898298›Full record

ArticleBreast cancer research : BCR2025

Global scoring method of Ki67 immunohistochemistry in breast cancer demonstrates improved concordance using real-world multi-institutional data.

Ceren Boyaci, Wenwen Sun, Johan Hartman, Balázs Ács

Abstract readMulticenter Study
In one paragraph

Article in Breast cancer research : BCR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ceren BoyaciDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Wenwen SunDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Johan HartmanDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden.
Balázs ÁcsDepartment of Oncology and Pathology, Karolinska Institutet, Stockholm, Sweden. balazs.acs@ki.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ki67 is a broadly available biomarker of proliferation with various approaches to its evaluation in breast cancer. The International Ki67 in Breast Cancer Working Group (IKWG) recommends calculating Ki67 globally across the tumor area, as this method offers high interobserver concordance. These recommendations have been integrated into many international breast cancer guidelines (ASCO, ESMO), yet there is no real-world data on if it improved inter-pathologists and inter-laboratory variability. Here, we present the first real-world data on the variability and impact of Ki67 scores on clinical decision-making in breast cancer when using hotspot scoring and after implementing IKWG global scoring method in clinical practice. We extracted hotspot and global scoring results from 4313 breast cancer patients from routine diagnostics, categorizing the scores into three clinical risk groups over a one-year period across two large breast centers in Stockholm, Sweden. Variability between pathologists was not clinically significant. The global scoring method improved inter-laboratory consistency but also led to a notable increase in cases classified as intermediate at both centers This has been captured in the 2022 Swedish clinical breast cancer guidelines recommending molecular profiling test for patients with Grade II, global Ki67 intermediate score, T1c / T2 breast cancer. To conclude, our findings demonstrate acceptable consistency in Ki67 scores among individual pathologists across both scoring methods, however high inter-laboratory variability was observed with hot spot scoring. Global Ki67 scoring demonstrated low inter-laboratory variability in real world breast cancer care, thereby increasing the reliability of Ki67 assessment in clinical decision-making.

Indexed as

Biomarkers, TumorBreast NeoplasmsImmunohistochemistryKi-67 AntigenAdultAgedClinical Decision-MakingFemaleHumansMiddle AgedNeoplasm GradingObserver VariationReproducibility of ResultsSwedenBiomarkers, TumorKi-67 AntigenMKI67 protein, humanBreast cancerGlobal scoringIKWGInterobserver variabilityKi67

Identifiers

PMID40898298
PMCPMC12406372

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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.