Differential Diagnosis of Malignant Pleural Mesothelioma on Cytology: A Gene Expression Panel versus BRCA1-Associated Protein 1 and p16 Tests.


Journal

The Journal of molecular diagnostics : JMD
ISSN: 1943-7811
Titre abrégé: J Mol Diagn
Pays: United States
ID NLM: 100893612

Informations de publication

Date de publication:
04 2020
Historique:
received: 19 02 2019
revised: 16 09 2019
accepted: 20 12 2019
pubmed: 10 2 2020
medline: 5 6 2021
entrez: 10 2 2020
Statut: ppublish

Résumé

Pleural effusions are among the first clinical manifestations of malignant pleural mesothelioma (MPM) and often constitute the only available material for diagnosis. Although an MPM diagnosis can be reliable on cytology, the reported sensitivity is low (30% to 75%). Particularly, it can be hard to discriminate epithelioid MPM, the most common histotype, from reactive mesothelial hyperplasia (MH). Currently, BRCA1-associated protein 1 (BAP1) and CDKN2A (p16), evaluated by immunohistochemistry and fluorescent in situ hybridization, respectively, are the most valuable markers to discriminate MPM and MH. Both markers have a high specificity, but their sensitivity is not always satisfying, even when used together. We have recently developed a 117-gene expression panel, based on Nanostring technology, able to differentiate epithelioid MPM from MH pleural tissues better than BAP1 and p16. Herein, we evaluated the efficacy of the same panel on an independent retrospective cohort of 23 MPM and 11 MH pleural effusions (cell blocks and smears). The overall sensitivity and specificity of the panel were equal to 0.9565 and 1, respectively. Moreover, the panel performance was compared with BAP1 and p16 on 25 cell blocks. Sensitivity levels of gene panel, BAP1 alone, p16 alone, and BAP1 plus p16 were 1, 0.5882, 0.4706, and 0.7647, respectively. Specificity was always 1. Although further validation is needed, this gene panel could really facilitate patients' management, allowing a definitive MPM diagnosis directly on pleural effusions.

Identifiants

pubmed: 32036091
pii: S1525-1578(20)30019-2
doi: 10.1016/j.jmoldx.2019.12.009
pii:
doi:

Substances chimiques

BAP1 protein, human 0
Biomarkers, Tumor 0
Cyclin-Dependent Kinase Inhibitor p16 0
Tumor Suppressor Proteins 0
Ubiquitin Thiolesterase EC 3.4.19.12

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

457-466

Informations de copyright

Copyright © 2020 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

Auteurs

Rossella Bruno (R)

Unit of Pathological Anatomy, University Hospital of Pisa, Pisa, Italy.

Greta Alì (G)

Unit of Pathological Anatomy, University Hospital of Pisa, Pisa, Italy.

Anello M Poma (AM)

Department of Surgical, Medical, Molecular Pathology and Critical Area, University of Pisa, Pisa, Italy.

Agnese Proietti (A)

Unit of Pathological Anatomy, University Hospital of Pisa, Pisa, Italy.

Roberta Libener (R)

Pathology Unit, SS Antonio and Biagio General Hospital, Alessandria, Italy.

Narciso Mariani (N)

Pathology Unit, SS Antonio and Biagio General Hospital, Alessandria, Italy.

Cristina Niccoli (C)

Unit of Pathological Anatomy, University Hospital of Pisa, Pisa, Italy.

Antonio Chella (A)

Unit of Pneumology, University Hospital of Pisa, Pisa, Italy.

Alessandro Ribechini (A)

Endoscopic Section of Pneumology, University Hospital of Pisa, Pisa, Italy.

Federica Grosso (F)

Mesothelioma Unit, SS Antonio and Biagio General Hospital, Alessandria, Italy.

Gabriella Fontanini (G)

Department of Surgical, Medical, Molecular Pathology and Critical Area, University of Pisa, Pisa, Italy. Electronic address: gabriella.fontanini@med.unipi.it.

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Classifications MeSH