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. 2023 Sep 14;13(18):2945.
doi: 10.3390/diagnostics13182945.

New Immunohistochemical Markers for Pleural Mesothelioma Subtyping

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New Immunohistochemical Markers for Pleural Mesothelioma Subtyping

Iosè Di Stefano et al. Diagnostics (Basel). .

Abstract

Pleural mesothelioma (PM) comprises three main subtypes: epithelioid, biphasic and sarcomatoid, which have different impacts on prognosis and treatment definition. However, PM subtyping can be complex given the inter- and intra-tumour morphological heterogeneity. We aim to use immunohistochemistry (IHC) to evaluate five markers (Mesothelin, Claudin-15, Complement Factor B, Plasminogen Activator Inhibitor 1 and p21-activated Kinase 4), whose encoding genes have been previously reported as deregulated among PM subtypes. Immunohistochemical expressions were determined in a case series of 73 PMs, and cut-offs for the epithelioid and non-epithelioid subtypes were selected. Further validation was performed on an independent cohort (30 PMs). For biphasic PM, the percentage of the epithelioid component was assessed, and IHC evaluation was also performed on the individual components separately. Mesothelin and Claudin-15 showed good sensitivity (79% and 84%) and specificity (84% and 73%) for the epithelioid subtype. CFB and PAK4 had inferior performance, with higher sensitivity (89% and 84%) but lower specificity (64% and 36%). In the biphasic group, all markers showed different expression when comparing epithelioid with sarcomatoid areas. Mesothelin, Claudin-15 and CFB can be useful in subtype discrimination. PAI1 and PAK4 can improve component distinction in biphasic PM.

Keywords: Claudin-15; Complement Factor B (CFB); Mesothelin; Plasminogen Activator Inhibitor 1 (PAI1); immunohistochemistry; p21-activated kinase 4 (PAK4); pleural mesothelioma; subtypes.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(A) An example of epithelioid mesothelioma (hematoxylin and eosin stain); (B) diffuse and strong membranous expression for Mesothelin; (C) Claudin-15 showing diffuse cytoplasmatic expression; (D) diffuse cytoplasmatic expression for CFB (magnification ×100).
Figure 2
Figure 2
A case of sarcomatoid mesothelioma (A) with malignant spindle cell growth (hematoxylin and eosin stain); (B) PAI1 and (C) PAK4 diffuse expression (magnification ×100).
Figure 3
Figure 3
A case of biphasic mesothelioma. (A) Haematoxylin and eosin stain with the epithelioid (left) and the sarcomatoid component (right); (B) Mesothelin, (C) Claudin-15 and (D) CFB higher expression in epithelioid component; (E) PAI1 and (F) PAK4 higher expression in sarcomatoid component (magnification ×100).

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