The 2021 WHO Classification of Tumors of the Pleura: Advances Since the 2015 Classification.
Biomarkers, Tumor
/ genetics
Homozygote
Humans
In Situ Hybridization, Fluorescence
Lung Neoplasms
/ pathology
Mesothelioma
/ pathology
Mesothelioma, Malignant
Pleura
/ pathology
Pleural Neoplasms
/ pathology
Sequence Deletion
Tumor Suppressor Proteins
/ genetics
Ubiquitin Thiolesterase
/ genetics
World Health Organization
Histopathology
Mesothelioma
Pleura
World Health Organization classification
Journal
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235
Informations de publication
Date de publication:
05 2022
05 2022
Historique:
received:
29
10
2021
revised:
14
12
2021
accepted:
31
12
2021
pubmed:
14
1
2022
medline:
27
4
2022
entrez:
13
1
2022
Statut:
ppublish
Résumé
Substantial changes in the 2021 WHO Classification of Tumors of the Pleura and Pericardium since the 2015 WHO Classification include the following: (1) pleural and pericardial tumors have been combined in one chapter whereas in the 2015 WHO, pericardial tumors were classified with cardiac tumors; (2) well-differentiated papillary mesothelioma has been renamed well-differentiated papillary mesothelial tumor given growing evidence that these tumors exhibit relatively indolent behavior; (3) localized and diffuse mesothelioma no longer include the term "malignant" as a prefix; (4) mesothelioma in situ has been added to the 2021 classification because these lesions can now be recognized by loss of BAP1 and/or MTAP by immunohistochemistry and/or CDKN2A homozygous deletion by fluorescence in situ hybridization; (5) the three main histologic subtypes (i.e., epithelioid, biphasic, and sarcomatoid) remain the same but architectural patterns and cytologic and stromal features are more formally incorporated into the 2021 classification on the basis of their prognostic significance; (6) nuclear grading for epithelioid diffuse mesothelioma is introduced, and it is recommended to record this and other histologically prognostic features in pathology reports; (7) BAP1, EZH2, and MTAP immunohistochemistry have been found to be useful in separating benign mesothelial proliferations from mesothelioma; (8) biphasic mesothelioma can be diagnosed in small biopsies having both epithelioid and sarcomatoid components even if the amount of one component is less than 10%; and (9) the most frequently altered genes in diffuse pleural mesothelioma include BAP1, CDKN2A, NF2, TP53, SETD2, and SETDB1.
Identifiants
pubmed: 35026477
pii: S1556-0864(22)00026-0
doi: 10.1016/j.jtho.2021.12.014
pii:
doi:
Substances chimiques
Biomarkers, Tumor
0
Tumor Suppressor Proteins
0
Ubiquitin Thiolesterase
EC 3.4.19.12
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
608-622Informations de copyright
Copyright © 2022 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.