The 2021 WHO Classification of Tumors of the Pleura: Advances Since the 2015 Classification
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...
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Published in | Journal of thoracic oncology Vol. 17; no. 5; pp. 608 - 622 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.05.2022
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Abstract | 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. |
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AbstractList | 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. 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.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. |
Author | Nicholson, Andrew G. Roggli, Victor Travis, William D. Sauter, Jennifer L. Attanoos, Richard L. Galateau-Salle, Francoise Dacic, Sanja Kadota, Kyuichi Butnor, Kelly J. Tsao, Ming-Sound Churg, Andrew Khoor, Andras Husain, Aliya N. Schmitt, Fernando |
Author_xml | – sequence: 1 givenname: Jennifer L. surname: Sauter fullname: Sauter, Jennifer L. email: sauterj@mskcc.org organization: Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York – sequence: 2 givenname: Sanja surname: Dacic fullname: Dacic, Sanja organization: Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania – sequence: 3 givenname: Francoise surname: Galateau-Salle fullname: Galateau-Salle, Francoise organization: MESOPATH Centre Leon Berard, Lyon, France – sequence: 4 givenname: Richard L. surname: Attanoos fullname: Attanoos, Richard L. organization: Department of Cellular Pathology, University Hospital of Wales and School of Medicine, Cardiff University, Cardiff, Wales, United Kingdom – sequence: 5 givenname: Kelly J. surname: Butnor fullname: Butnor, Kelly J. organization: Department of Pathology & Laboratory Medicine, The University of Vermont Medical Center, Burlington, Vermont – sequence: 6 givenname: Andrew surname: Churg fullname: Churg, Andrew organization: Department of Pathology and Laboratory Medicine, Vancouver General Hospital and The University of British Columbia, Vancouver, British Columbia, Canada – sequence: 7 givenname: Aliya N. surname: Husain fullname: Husain, Aliya N. organization: Department of Pathology, The University of Chicago, Chicago, Illinois – sequence: 8 givenname: Kyuichi surname: Kadota fullname: Kadota, Kyuichi organization: Department of Pathology, Faculty of Medicine, Shimane University, Izumo, Japan – sequence: 9 givenname: Andras surname: Khoor fullname: Khoor, Andras organization: Department of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, Florida – sequence: 10 givenname: Andrew G. surname: Nicholson fullname: Nicholson, Andrew G. organization: Royal Brompton and Harefield Hospitals, and National Heart and Lung Institute, Imperial College, London, United Kingdom – sequence: 11 givenname: Victor surname: Roggli fullname: Roggli, Victor organization: Department of Pathology, Duke University Medical Center, Durham, North Carolina – sequence: 12 givenname: Fernando surname: Schmitt fullname: Schmitt, Fernando organization: RISE@CINTESIS, Medical Faculty of Porto University, Porto, Portugal – sequence: 13 givenname: Ming-Sound surname: Tsao fullname: Tsao, Ming-Sound organization: Department of Pathology, Princess Margaret Cancer Centre, University Health Network, Toronto, Canada – sequence: 14 givenname: William D. surname: Travis fullname: Travis, William D. organization: Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York |
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Copyright | 2022 International Association for the Study of Lung Cancer Copyright © 2022 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved. |
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SubjectTerms | Biomarkers, Tumor - genetics Histopathology Homozygote Humans In Situ Hybridization, Fluorescence Lung Neoplasms - pathology Mesothelioma Mesothelioma - pathology Mesothelioma, Malignant Pleura Pleura - pathology Pleural Neoplasms - pathology Sequence Deletion Tumor Suppressor Proteins - genetics Ubiquitin Thiolesterase - genetics World Health Organization World Health Organization classification |
Title | The 2021 WHO Classification of Tumors of the Pleura: Advances Since the 2015 Classification |
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