Re-evaluation of HER2 status in 606 breast cancers-gene protein assay on tissue microarrays versus routine pathological assessment.


Journal

Virchows Archiv : an international journal of pathology
ISSN: 1432-2307
Titre abrégé: Virchows Arch
Pays: Germany
ID NLM: 9423843

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 15 11 2019
accepted: 04 02 2020
revised: 13 01 2020
pubmed: 23 2 2020
medline: 30 7 2020
entrez: 22 2 2020
Statut: ppublish

Résumé

Human epidermal growth factor receptor 2 (HER2) status in breast cancer is routinely determined through immunohistochemistry (IHC) and/or in situ hybridisation (ISH) performed on whole tissue sections (WS). The purpose was to evaluate whether a gene protein assay (GPA) combining IHC with ISH, performed on breast cancer tissue microarray (TMA), is suitable for large-scale retrospective HER2 status evaluation. TMAs from 606 tumours from a Swedish population-based cohort (2005-2012) were stained with GPA. GPA IHC on TMA yielded weaker staining than IHC on WS during routine pathological assessment (86.0% agreement). However, final HER2 status agreement between GPA on TMA and WS based on both IHC and ISH was 97.7%. Only 14 tumours were discordant and one tumour with IHC score 1+ on both TMA and WS was HER2 amplified on TMA. In conclusion, GPA on TMA is suitable for large-scale retrospective evaluation of HER2 status.

Identifiants

pubmed: 32080761
doi: 10.1007/s00428-020-02768-x
pii: 10.1007/s00428-020-02768-x
pmc: PMC7371653
doi:

Substances chimiques

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

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

317-320

Subventions

Organisme : Cancerfonden
ID : 2017/368
Organisme : Medicinska Fakulteten, Lunds Universitet
ID : NA
Organisme : Fru Berta Kamprads Stiftelse
ID : 2017-4
Organisme : Region Skåne
ID : 40620
Organisme : Skånes universitetssjukhus
ID : NA

Références

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Auteurs

Emma Sandén (E)

Department of Clinical Sciences in Lund, Oncology and Pathology, Faculty of Medicine, Lund University Cancer Center / Kamprad, Lund University and Skåne University Hospital, Lund, Sweden.

Somayeh Khazaei (S)

Department of Clinical Sciences in Lund, Oncology and Pathology, Faculty of Medicine, Lund University Cancer Center / Kamprad, Lund University and Skåne University Hospital, Lund, Sweden.

Helga Tryggvadottir (H)

Department of Clinical Sciences in Lund, Oncology and Pathology, Faculty of Medicine, Lund University Cancer Center / Kamprad, Lund University and Skåne University Hospital, Lund, Sweden.

Signe Borgquist (S)

Department of Clinical Sciences in Lund, Oncology and Pathology, Faculty of Medicine, Lund University Cancer Center / Kamprad, Lund University and Skåne University Hospital, Lund, Sweden.
Departments of Oncology and Clinical Medicine, Aarhus University and Aarhus University Hospital, Aarhus, Denmark.

Karolin Isaksson (K)

Department of Clinical Sciences in Lund, Surgery, Faculty of Medicine, Lund University Cancer Center, Lund University and Skåne University Hospital, Lund, Sweden, and Central Hospital Kristianstad, Kristianstad, Sweden.

Karin Jirström (K)

Department of Clinical Sciences in Lund, Oncology and Pathology, Faculty of Medicine, Lund University Cancer Center / Kamprad, Lund University and Skåne University Hospital, Lund, Sweden.

Helena Jernström (H)

Department of Clinical Sciences in Lund, Oncology and Pathology, Faculty of Medicine, Lund University Cancer Center / Kamprad, Lund University and Skåne University Hospital, Lund, Sweden. helena.jernstrom@med.lu.se.

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Classifications MeSH