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The worsening impact of programmed cell death ligand 1 in ovarian clear cell carcinomas.

Authors :
Matsuura, Hiroko
Miyamoto, Morikazu
Hada, Taira
Ishibashi, Hiroki
Iwahashi, Hideki
Kakimoto, Soichiro
Suzuki, Rie
Ito, Tsubasa
Suminokura, Jin
Tsuda, Hitoshi
Takano, Masashi
Source :
Archives of Gynecology & Obstetrics. Dec2022, Vol. 306 Issue 6, p2133-2142. 10p.
Publication Year :
2022

Abstract

Purpose: To investigate the clinical significance of programmed cell death ligand 1 (PD-L1) expression in ovarian clear cell carcinoma (CCC). Materials and methods: Patients with CCC who underwent primary surgery at our hospital between 1984 and 2014 were enrolled in this study. PD-L1 and mismatch repair (MMR) protein expression in tumor cells, tumor-infiltrating lymphocytes (TILs), including cluster of differentiation (CD) 8, CD4, forkhead box P3 (FOXP3), programmed cell death 1 (PD-1), and BAF250a, were evaluated using immunohistochemistry. The association between PD-L1 expression, clinicopathological features, prognosis, and expression of several proteins was investigated. Results: Of the 125 patients with CCC, 17 had negative PD-L1 and 108 had positive PD-L1. Patients with positive PD-L1 expression showed a lower response to chemotherapy (p = 0.01). In addition, patients with positive PD-L1 showed worse progression-free survival (PFS, p = 0.01) and overall survival (OS, p = 0.01) than that in patients with negative PD-L1 expression. Multivariate analyses for PFS and OS showed that PD-L1 expression was an independent prognostic factor for PFS (hazard ratio [HR] 7.81, p < 0.01) and OS (HR 12.90, p < 0.01). PD-L1 expression was not associated with the expression of several TILs or proteins. Conclusion: The expression of PD-L1 was related to a lower response to chemotherapy and worse prognosis in CCC. These results may be useful for the development of new treatments. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09320067
Volume :
306
Issue :
6
Database :
Academic Search Index
Journal :
Archives of Gynecology & Obstetrics
Publication Type :
Academic Journal
Accession number :
160049354
Full Text :
https://doi.org/10.1007/s00404-022-06582-5