TY - JOUR
T1 - The 2021 WHO Classification of Tumors of the Pleura
T2 - Advances Since the 2015 Classification
AU - Sauter, Jennifer L.
AU - Dacic, Sanja
AU - Galateau-Salle, Francoise
AU - Attanoos, Richard L.
AU - Butnor, Kelly J.
AU - Churg, Andrew
AU - Husain, Aliya N.
AU - Kadota, Kyuichi
AU - Khoor, Andras
AU - Nicholson, Andrew G.
AU - Roggli, Victor
AU - Schmitt, Fernando
AU - Tsao, Ming Sound
AU - Travis, William D.
N1 - Funding Information:
Disclosure: Dr. Attanoos reports providing expert testimony for claimants, defendants, and joint basis in personal injury asbestos claims. Dr. Nicholson reports receiving personal fees from Merck, Boehringer Ingelheim, Novartis, AstraZeneca, Bristol-Myers Squibb, Roche, AstraZeneca, AbbVie, Oncologica, UptoDate, European Society of Oncology, Liberum, and Takeda UK and grants and personal fees from Pfizer, outside of the submitted work. Dr. Roggli reports consulting with attorneys for plaintiffs and defendants in asbestos litigation. Dr. Tsao reports receiving grants and personal fees from AstraZeneca and Bayer and personal fees from Bristol-Myers Squibb, Amgen, Daiichi Sankyo, Eli Lilly, and AbbVie, outside of the submitted work. The remaining authors declare no conflict of interest.
Publisher Copyright:
© 2022 International Association for the Study of Lung Cancer
PY - 2022/5
Y1 - 2022/5
N2 - 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.
AB - 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.
KW - Histopathology
KW - Mesothelioma
KW - Pleura
KW - World Health Organization classification
UR - http://www.scopus.com/inward/record.url?scp=85124043808&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85124043808&partnerID=8YFLogxK
U2 - 10.1016/j.jtho.2021.12.014
DO - 10.1016/j.jtho.2021.12.014
M3 - Review article
C2 - 35026477
AN - SCOPUS:85124043808
SN - 1556-0864
VL - 17
SP - 608
EP - 622
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 5
ER -