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Association of Androgen Receptor Expression on Tumor Cells and PD-L1 Expression in Muscle-Invasive and Metastatic Urothelial Carcinoma: Insights for Clinical Research.
- Source :
-
Clinical genitourinary cancer [Clin Genitourin Cancer] 2018 Apr; Vol. 16 (2), pp. e403-e410. Date of Electronic Publication: 2017 Oct 07. - Publication Year :
- 2018
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Abstract
- Background: Limited information is available regarding the use of androgen receptor (AR) immunohistochemical expression in muscle-invasive or metastatic urothelial carcinoma. We aimed to evaluate the frequency of AR expression by tumor cells (TC), its prognostic role, and its relationship with programmed cell-death ligand 1 (PD-L1) expression in these patients.<br />Patients and Methods: From September 2015 to January 2017, we collected tissue from patients who received platinum-based chemotherapy at our center. Immunohistochemistry for AR was performed (1% cutoff of TC). PD-L1 coexpression, by TC or immune cells (1% cutoff), was also analyzed. Molecular analysis of AR gene was performed by sequencing of exons 5 to 8 and by fluorescence in-situ hybridization analysis. Cox models for overall survival (OS), adjusted for stage, visceral metastases, and platinum type, were fitted.<br />Results: A total of 110 patients had tumor samples stained. Overall, 48 (43.6%) had AR-expressing TC: 19 (17.3%) had 1%-5% expression, 15 (13.6%) 5%-25% expression, and 14 (12.7%) > 25% expression. Among the latter, 7 had molecularly evaluated tumor tissue: no AR gene mutations or amplifications were found, but polysomy of Xq chromosome was seen. PD-L1 expression by TC and immunohistochemistry concordantly decreased with increasing levels of AR expression by TC. In Cox analyses, AR expression was not associated with OS, both on univariable (P = .477) and multivariable (P = .505) analyses.<br />Conclusion: AR is frequently expressed in patients with muscle-invasive and advanced urothelial carcinoma, and it does not seem to be prognostic for OS. The AR pathway is worthy of clinical studies to assess its synergistic action with anti-PD-L1 therapy.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Aged
Carcinoma, Transitional Cell genetics
Carcinoma, Transitional Cell metabolism
Chromosomes, Human, X genetics
Female
Gene Expression Regulation, Neoplastic
Humans
Male
Middle Aged
Receptors, Androgen genetics
Retrospective Studies
Sequence Analysis, DNA
Survival Analysis
Treatment Outcome
Urologic Neoplasms genetics
Urologic Neoplasms metabolism
B7-H1 Antigen metabolism
Carcinoma, Transitional Cell drug therapy
Platinum therapeutic use
Receptors, Androgen metabolism
Urologic Neoplasms drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1938-0682
- Volume :
- 16
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Clinical genitourinary cancer
- Publication Type :
- Academic Journal
- Accession number :
- 29111177
- Full Text :
- https://doi.org/10.1016/j.clgc.2017.09.016