Evidence map›Paper›PMID 38218973›Full record

ArticleScientific reports2024

AI improves accuracy, agreement and efficiency of pathologists for Ki67 assessments in breast cancer.

Amanda Dy, Ngoc-Nhu Jennifer Nguyen, Julien Meyer, Melanie Dawe, Wei Shi, Dimitri Androutsos, Anthony Fyles, Fei-Fei Liu, Susan Done, April Khademi

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Artificial intelligence-based quantification of epidermal proliferation and apoptosis in human skin.JID innovations : skin science from molecules to population health · 2026
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  19. Patient outcomes and clinician perspectives following one year ofTranslational breast cancer research : a journal focusing on translational research in breast cancer · 2025
    Article
  20. Article
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

10 authors.

Amanda DyElectrical, Computer, and Biomedical Engineering, Toronto Metropolitan University, Toronto, ON, Canada. amanda.dy@torontomu.ca.
Ngoc-Nhu Jennifer NguyenDepartment of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
Julien MeyerSchool of Health Services Management, Toronto Metropolitan University, Toronto, ON, Canada.
Melanie DawePrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Wei ShiPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Dimitri AndroutsosElectrical, Computer, and Biomedical Engineering, Toronto Metropolitan University, Toronto, ON, Canada.
Anthony FylesPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Fei-Fei LiuPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Susan DonePrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
April KhademiElectrical, Computer, and Biomedical Engineering, Toronto Metropolitan University, Toronto, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Ki-67 proliferation index (PI) guides treatment decisions in breast cancer but suffers from poor inter-rater reproducibility. Although AI tools have been designed for Ki-67 assessment, their impact on pathologists' work remains understudied. 90 international pathologists were recruited to assess the Ki-67 PI of ten breast cancer tissue microarrays with and without AI. Accuracy, agreement, and turnaround time with and without AI were compared. Pathologists' perspectives on AI were collected. Using AI led to a significant decrease in PI error (2.1% with AI vs. 5.9% without AI, p < 0.001), better inter-rater agreement (ICC: 0.70 vs. 0.92; Krippendorff's α: 0.63 vs. 0.89; Fleiss' Kappa: 0.40 vs. 0.86), and an 11.9% overall median reduction in turnaround time. Most pathologists (84%) found the AI reliable. For Ki-67 assessments, 76% of respondents believed AI enhances accuracy, 82% said it improves consistency, and 83% trust it will improve efficiency. This study highlights AI's potential to standardize Ki-67 scoring, especially between 5 and 30% PI-a range with low PI agreement. This could pave the way for a universally accepted PI score to guide treatment decisions, emphasizing the promising role of AI integration into pathologist workflows.

Indexed as

Breast NeoplasmsFemaleHumansImmunohistochemistryKi-67 AntigenPathologistsReproducibility of ResultsKi-67 Antigen

Identifiers

PMID38218973
PMCPMC10787826

What OpenQuestion holds

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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.