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PD-1, PD-L1 and cAMP immunohistochemical expressions are associated with worse oncological outcome in patients with bladder cancer.

Authors :
Russo GI
Musso N
Lo Giudice A
Asmundo MG
Di Mauro M
Bonacci PG
Massimino M
Bivona D
Stefani S
Pricoco E
Ferro M
Camarda M
Cimino S
Morgia G
Caltabiano R
Broggi G
Source :
Journal of cancer research and clinical oncology [J Cancer Res Clin Oncol] 2023 Jul; Vol. 149 (7), pp. 3681-3690. Date of Electronic Publication: 2022 Aug 16.
Publication Year :
2023

Abstract

Purpose: In this study, we aimed to identify prognostic factors of cancer mortality in patients who received radical cystectomy and to identify genomic alterations in a sub-cohort of patients with locally advanced (pT3-4) and/or positive lymph nodes bladder cancer (BC).<br />Methods: We collected 101 BC samples from 2010 to 2018 who previously received radical cystectomy. Immunohistochemical slides were evaluated for PPAR, cAMP, IMP3, Ki67, CDK4, POU5F1, Cyclin E and MDM2, p65, CD3, CD4, CD8, CD20, CD68, CD163, FOXP3, PD-1 and PD-L1 expression. We calculated a prognostic score (PS) based on the positivity to PD-1, PD-L1 and of cAMP (final score ranging from 0 to 3). DNA of each sample have been used for sequencing by NGS in a sub-cohort of 6 patients with locally advanced (pT3-4) and/or positive lymph nodes BC.<br />Results: PD-1 <superscript>+</superscript> (HR [hazard ratio] 2.59; p = 0.04), PD-L1 <superscript>+</superscript> (HR = 6.46; p < 0.01) and cAMP <superscript>+</superscript> (HR 3.04; p = 0.02) were independent predictors of cancer-specific mortality (CSM). Increase of PS (score = 0 as reference) was associated with CSM, 0.81 (p = 0.80), 4.72 (p = 0.01) and 10.51 (p < 0.0) for PS 1, 2 and 3, respectively. ERBB2 was the gene most frequently mutated.<br />Conclusion: BC exhibited heterogenous protein expression and variable genomic features. Identification of expression of PD-1, PD-L1 and cAMP could help in predicting oncological outcomes.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
1432-1335
Volume :
149
Issue :
7
Database :
MEDLINE
Journal :
Journal of cancer research and clinical oncology
Publication Type :
Academic Journal
Accession number :
35972693
Full Text :
https://doi.org/10.1007/s00432-022-04262-0