The "Brescia panel" (Claudin‐4 and BRCA‐associated protein 1) in the differential diagnosis of mesotheliomas with epithelioid features versus metastatic carcinomas. Issue 4 (12th October 2020)

• Record Type: Journal Article
• Authors: Bernardi, Livia; Bizzarro, Tommaso; Pironi, Flavio; Szymczuk, Stefania; Buda, Raffaella; Fabbri, Enrica; Di Claudio, Giovanni; Rossi, Giulio
• Is Part Of: Cancer cytopathology. Volume 129:Issue 4(2021)
• Page Start: 275
• Page End: 282
• Publication Date: 2020-10-12
• Subjects: BRCA‐associated protein 1 (BAP1) -- Claudin‐4 -- diagnostic cytology -- effusion cytology -- immunocytochemistry -- malignant mesothelioma -- malignant mesothelioma versus metastatic carcinoma -- metastatic carcinoma; Cancer -- Cytopathology -- Periodicals; Pathology, Cellular -- Periodicals; Cytology -- Technique -- Periodicals; 611.01815
• DOI: 10.1002/cncy.22368
• Languages: English
• ISSNs: 1934-662X

Abstract

Abstract : Background: The distinction between mesothelioma with epithelioid features and metastatic carcinoma may be challenging, particularly on cytology. A novel 2‐hit Claudin‐4 and BRCA‐associated protein 1 (BAP1) panel was investigated. Methods: The objective of this study was to determine the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of the panel on cytology from pleural effusions and matched biopsies, including 49 malignant mesotheliomas on cytology with 43 matched biopsies, 49 normal/reactive mesothelial proliferations, and 49 pleural metastatic carcinomas from different primaries with 21 matched pleural biopsies. The diagnostic role of the 4 categories obtained by crossing the immunostaining results was analyzed. Results: Claudin‐4 strongly stained all metastatic carcinomas and tested completely negative in normal mesothelium, benign reactive mesothelial hyperplasia, and malignant mesothelioma. All normal and benign mesothelial proliferations and all carcinomas except 1 were immunoreactive for BAP1, whereas BAP1 loss was observed in 88% of malignant mesotheliomas. The expression of Claudin‐4 alone excluded all benign and malignant mesothelial growth, consistently characterizing all metastatic carcinomas. Double negativity was evident in all malignant mesotheliomas, and double positivity was observed in all metastatic carcinomas. BAP1‐positive/Claudin‐4–negative status was observed only in malignant mesotheliomas and benign mesothelial proliferations. A single metastatic anal squamous cell carcinoma had BAP1‐negative/Claudin‐4–positive staining. Conclusions: Claudin‐4 expression was completely specific and sensitive for metastatic carcinoma, excluding mesothelial proliferations. BAP1 staining characterized 98% of metastatic carcinomas and 100% of benign mesothelial proliferations, whereas negativity was observed almost exclusively in mesotheliomas. This 2‐hit panel is probably the best compromise for differentiating malignant mesothelioma and metastatic carcinoma on either cytology or biopsy specimens. Abstract : Claudin‐4 expression in effusion cytology is completely specific and sensitive for metastatic carcinoma, excluding mesothelial proliferations; otherwise, BRCA1‐associated protein 1 (BAP1) staining characterizes 98% of metastatic carcinomas and 100% of benign mesothelial proliferations, whereas negativity is almost exclusively disclosed in mesothelioma. This 2‐hit Claudin‐4/BAP1 panel is probably the best compromise in differentiating malignant mesothelioma and metastatic carcinoma on either cytology or biopsy specimens.