Improved concordance of challenging human epidermal growth factor receptor 2 dual in-situ hybridisation cases with the use of a digital image analysis algorithm in breast cancer.


Journal

Histopathology
ISSN: 1365-2559
Titre abrégé: Histopathology
Pays: England
ID NLM: 7704136

Informations de publication

Date de publication:
Oct 2023
Historique:
revised: 09 06 2023
received: 25 04 2023
accepted: 12 06 2023
medline: 13 9 2023
pubmed: 27 6 2023
entrez: 27 6 2023
Statut: ppublish

Résumé

Accurate assessment of human epidermal growth factor receptor 2 (HER2) expression by HER2 immunohistochemistry and in-situ hybridisation (ISH) is critical for the management of patients with breast cancer. The revised 2018 ASCO/CAP guidelines define 5 groups based on HER2 expression and copy number. Manual pathologist quantification by light microscopy of equivocal and less common HER2 ISH groups (groups 2-4) can be challenging, and there are no data on interobserver variability in reporting of these cases. We sought to determine whether a digital algorithm could improve interobserver variability in the assessment of difficult HER2 ISH cases. HER2 ISH was evaluated in a cohort enriched for less common HER2 patterns using standard light microscopy versus analysis of whole slide images using the Roche uPath HER2 dual ISH image analysis algorithm. Standard microscopy demonstrated significant interobserver variability with a Fleiss's kappa value of 0.471 (fair-moderate agreement) improving to 0.666 (moderate-good) with the use of the algorithm. For HER2 group designation (groups 1-5), there was poor-moderate reliability between pathologists by microscopy [intraclass correlation coefficient (ICC) = 0.526], improving to moderate-good agreement (ICC = 0.763) with the use of the algorithm. In subgroup analysis, the algorithm improved concordance particularly in groups 2, 4 and 5. Time to enumerate cases was also significantly reduced. This work demonstrates the potential of a digital image analysis algorithm to improve the concordance of pathologist HER2 amplification status reporting in less common HER2 groups. This has the potential to improve therapy selection and outcomes for patients with HER2-low and borderline HER2-amplified breast cancers.

Identifiants

pubmed: 37366040
doi: 10.1111/his.15000
doi:

Substances chimiques

ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Biomarkers, Tumor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

647-656

Subventions

Organisme : RCPA Quality Assurance Programs Research
Organisme : Mater Foundation
Organisme : Roche Diagnostics
Organisme : University of Queensland Graduate School
Organisme : Mater Foundation and Equity Trustees (The KC & BM Thomson Memorial Fund)

Informations de copyright

© 2023 The Authors. Histopathology published by John Wiley & Sons Ltd.

Références

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Auteurs

Madeline Gough (M)

Mater Pathology, Duncombe Building, Raymond Terrace, South Brisbane, Australia.
Mater Research Institute, Translational Research Institute, Woolloongabba, Australia.

Cheng Liu (C)

Mater Pathology, Duncombe Building, Raymond Terrace, South Brisbane, Australia.
Faculty of Medicine, The University of Queensland, Herston, Australia.

Bhuvana Srinivasan (B)

Mater Pathology, Duncombe Building, Raymond Terrace, South Brisbane, Australia.

Lisa Wilkinson (L)

Mater Pathology, Duncombe Building, Raymond Terrace, South Brisbane, Australia.

Louisa Dunk (L)

Mater Pathology, Duncombe Building, Raymond Terrace, South Brisbane, Australia.

Yuanhao Yang (Y)

Mater Research Institute, Translational Research Institute, Woolloongabba, Australia.

Veronika Schreiber (V)

Mater Research Institute, Translational Research Institute, Woolloongabba, Australia.

Haitham Tuffaha (H)

Centre for the Business and Economics of Health, The University of Queensland, St Lucia, Australia.

Thomas Kryza (T)

Mater Research Institute, Translational Research Institute, Woolloongabba, Australia.

John D Hooper (JD)

Mater Research Institute, Translational Research Institute, Woolloongabba, Australia.

Sunil R Lakhani (SR)

Centre for Clinical Research, The University of Queensland, Herston, Australia.
Pathology Queensland, The Royal Brisbane Women's Hospital, Herston, Australia.

Cameron E Snell (CE)

Mater Pathology, Duncombe Building, Raymond Terrace, South Brisbane, Australia.
Mater Research Institute, Translational Research Institute, Woolloongabba, Australia.
Anatomical Pathology, Peter MacCallum Cancer Centre, Melbourne, Australia.

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