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Prognostic relevance of programmed cell death protein 1/programmed death-ligand 1 pathway in thymic malignancies with combined immunohistochemical and biomolecular approach.

Authors :
Berardi R
Goteri G
Brunelli A
Pagliaretta S
Paolucci V
Caramanti M
Rinaldi S
Refai M
Pompili C
Morgese F
Torniai M
Marcantognini G
Ricci G
Mazzanti P
Onofri A
Bianchi F
Sabbatini A
Cascinu S
Source :
Expert opinion on therapeutic targets [Expert Opin Ther Targets] 2020 Sep; Vol. 24 (9), pp. 937-943. Date of Electronic Publication: 2020 Jul 23.
Publication Year :
2020

Abstract

Background: The aim of the study was to investigate Programmed cell Death protein 1 (PD-1) and Programmed Death-Ligand 1 (PD-L1) and their mRNA expression in thymic epithelial tumors (TETs).<br />Research Design and Methods: We analyzed 68 samples of formalin-fixed paraffin-embedded tissue (63 thymomas and 5 thymic carcinomas). PD-1 and PD-L1 protein expression were evaluated by immunohistochemistry, and mRNA expression was evaluated by real-time PCR.<br />Results: M/F ratio was 33/35, and median age was 60.5 years. Twenty patients had Myasthenia Gravis (MG). In the subgroup with large tumors (>5 cm), PD-L1 mRNA overexpression was significantly associated with worse prognosis vs. patients with no mRNA overexpression (p = 0.0083) and simultaneous PD-L1 immunostaining (>1%); PD-L1 mRNA overexpression was significantly associated with worse prognosis, respect to patient with PD-L1 negative immunostaining, and no PD-L1 mRNA overexpression (p = 0.0178). The elderly patients (>60 years) with large tumors showed worse prognosis (p = 0.0395). PD-L1 immunostaining (>50%) resulted to be significantly associated with MG.<br />Conclusions: Our data suggest the potential involvement of the PD-1 and PD-L1 pathway in TETs' progression. According to our results, it may be helpful to design future trials with anti-PD-1 drugs to establish high-risk patients after surgery.

Details

Language :
English
ISSN :
1744-7631
Volume :
24
Issue :
9
Database :
MEDLINE
Journal :
Expert opinion on therapeutic targets
Publication Type :
Academic Journal
Accession number :
32662701
Full Text :
https://doi.org/10.1080/14728222.2020.1790529