Evidence map›Paper›PMID 42057919›Full record

ArticleJournal of pathology informatics2026

Defining hotspot for estimation of Ki-67 proliferation index of neuroendocrine tumors: QuPath algorithm vs. manual assessment.

Ruben Oganesyan, Osman Yilmaz, Yevgen Chornenkyy, Kanchan Kantekure, Yuho Ono, Buthania Hakamy, Nandan Padmanabha, Vikram Deshpande, Raul S Gonzalez, Monika Vyas

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Article in Journal of pathology informatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Ruben OganesyanBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Osman YilmazEmory University Hospital, Atlanta, GA, USA.
Yevgen ChornenkyyBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Kanchan KantekureBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Yuho OnoBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Buthania HakamyBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Nandan PadmanabhaBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Vikram DeshpandeBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.
Raul S GonzalezEmory University Hospital, Atlanta, GA, USA.
Monika VyasBeth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Ki-67 proliferation index (PI) is essential for grading well-differentiated neuroendocrine tumors (WD-NETs). Pathologists traditionally assess Ki-67 PI by identifying hotspots and manually counting the positive cells among negative cells, which is expressed as a percentage. We developed an algorithm to objectively determine Ki-67 hotspots and calculate PI in WD-NETs, comparing its results with pathologists' selected hotspots to assess reliability. Methods: Hotspots for gastroenteropancreatic WD-NETs ( Results: Pathologists showed moderate agreement (Fleiss's Kappa = 0.42, 80% agreement), whereas pathologist-algorithm agreement was fair (Cohen's Kappa = 0.32, 58.9% agreement). Among cases with pathologist consensus grade ( Conclusion: Manual Ki-67 hotspot assessment is subjective, leading to grading variability. Algorithm-based assessment enhances reproducibility, though this occasionally leads to tumor upgrading, highlighting the need for standardization and further validation.

Indexed as

Computer assisted gradingKi-67QuPathWell-differentiated neuroendocrine tumors

Identifiers

PMID42057919
PMCPMC13121424

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