Differential Diagnosis of Malignant Pleural Mesothelioma on Cytology: A Gene Expression Panel versus BRCA1-Associated Protein 1 and p16 Tests.
Aged
Biomarkers, Tumor
Cyclin-Dependent Kinase Inhibitor p16
/ genetics
Cytodiagnosis
Diagnosis, Differential
Female
Gene Expression Profiling
/ methods
Humans
Immunohistochemistry
In Situ Hybridization, Fluorescence
Male
Mesothelioma, Malignant
/ diagnosis
Middle Aged
Pleural Neoplasms
/ diagnosis
Reproducibility of Results
Sensitivity and Specificity
Tumor Suppressor Proteins
/ genetics
Ubiquitin Thiolesterase
/ genetics
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
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
457-466Informations de copyright
Copyright © 2020 Association for Molecular Pathology and American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.