The utility of P53 immunohistochemistry in the diagnosis of Barrett's oesophagus with indefinite for dysplasia.


Journal

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

Informations de publication

Date de publication:
Jun 2022
Historique:
revised: 09 02 2022
received: 20 12 2021
accepted: 06 03 2022
pubmed: 12 3 2022
medline: 24 5 2022
entrez: 11 3 2022
Statut: ppublish

Résumé

Barrett's oesophagus with indefinite for dysplasia (BE-IND) is a subjective diagnosis with a low interobserver agreement (IOA) among pathologists and uncertain clinical implications. This study aimed to assess the utility of p53 immunohistochemistry (p53-IHC) in assessing BE-IND specimens. Archive endoscopic biopsies with a BE-IND diagnosis from two academic centres were analysed. First, haematoxylin and eosin-stained slides (H&E) were reviewed by four expert gastrointestinal (GI) pathologists allocated into two groups (A and B). After a washout period of at least 8 weeks, H&E slides were reassessed side-to-side with p53-IHC available. We compared the rate of changed diagnosis and the IOA for all BE grades before and after p53-IHC. We included 216 BE-IND specimens from 185 patients, 44.0 and 32.9% of which were confirmed after H&E slide revision by groups A and B, respectively. More than half the cases were reclassified to a non-dysplastic BE (NDBE), while 5.6% of cases in group A and 7.4% in group B were reclassified to definite dysplasia. The IOA for NDBE, BE-IND, low-grade dysplasia (LGD) and high-grade dysplasia (HGD)/intramucosal cancer (IMC) was 0.31, 0.21, -0.03 and -0.02, respectively. Use of p53-IHC led to a >40% reduction in BE-IND diagnoses (P < 0.001) and increased IOA for all BE grades [κ = 0.46 (NDBE), 0.26 (BE-IND), 0.49 (LGD), 0.35 (HGD/IMC)]. An aberrant p53-IHC pattern significantly increased the likelihood of reclassifying BE-IND to definite dysplasia (odds ratio = 44.3, 95% confidence interval = 18.8-113.0). P53-IHC reduces the rate of BE-IND diagnoses and improves the IOA among pathologists when reporting BE with equivocal epithelial changes.

Identifiants

pubmed: 35274753
doi: 10.1111/his.14642
pmc: PMC9321087
doi:

Substances chimiques

Tumor Suppressor Protein p53 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1081-1090

Subventions

Organisme : Biomedical Research Centre

Informations de copyright

© 2022 The Authors. Histopathology published by John Wiley & Sons Ltd.

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Auteurs

Wladyslaw Januszewicz (W)

Early Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.
Department of Gastroenterology, Hepatology and Clinical Oncology, Centre of Postgraduate Medical Education, Warsaw, Poland.

Nastazja D Pilonis (ND)

Early Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.

Tarek Sawas (T)

Mayo Clinic, Rochester, Minnesota, USA.

Richard Phillips (R)

Early Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.

Maria O'Donovan (M)

Department of Histopathology, Addenbrooke's Hospital, Cambridge, UK.

Ahmad Miremadi (A)

Department of Histopathology, Addenbrooke's Hospital, Cambridge, UK.

Shalini Malhotra (S)

Department of Histopathology, Addenbrooke's Hospital, Cambridge, UK.

Monika Tripathi (M)

Department of Histopathology, Addenbrooke's Hospital, Cambridge, UK.

Adrienn Blasko (A)

Early Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.

David A Katzka (DA)

Mayo Clinic, Rochester, Minnesota, USA.

Rebecca C Fitzgerald (RC)

Early Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.

Massimiliano di Pietro (M)

Early Cancer Institute, Department of Oncology, University of Cambridge, Cambridge, UK.

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