Age and sex have no impact on expression levels of markers of immune cell infiltration and immune checkpoint pathways in patients with muscle-invasive urothelial carcinoma of the bladder treated with radical cystectomy.


Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 10 12 2018
accepted: 06 04 2019
pubmed: 19 4 2019
medline: 4 6 2019
entrez: 19 4 2019
Statut: ppublish

Résumé

Advanced age and female sex have been associated with worse outcomes in patients undergoing radical cystectomy for muscle-invasive bladder cancer. A reduced immune response has been implicated as a mechanism. The objective of our study was to analyze the expression patterns of various cellular proteins active in bladder cancer immune pathways, and assess the correlation between age, sex, and the expression of these immune markers. We obtained surgical tissue samples from equally distributed male/female patients with/without lymph node metastasis who had undergone radical cystectomy for urothelial carcinoma (UC) of the bladder (n = 50). Immunohistochemistry (IHC) for CD3 (cluster of differentiation), CD4, CD8, CD56, LAG-3 (lymphocyte-activation gene), TIM-3 (T-cell immunoglobulin and mucin-domain), PD-1 (programmed death) and PD-L1 molecules was performed and scored by a single pathologist (high versus low). Spearman's correlation and Chi square tests investigated the association between age, sex, and IHC results. Mean age at surgery was 67 years (range 50-78 years); all patients were Caucasians. The following percent of patients scored high for a stain: 18% CD3, 10% CD4, 0% CD8, 0% CD56, 20% LAG-3, 4% TIM-3, 0% PD-1 and 0% PD-L1. There was no association between patients' age, sex, and the expression of any of the immune markers (p > 0.05 for all). The association between advanced age, female sex, and worse outcomes in bladder cancer may be independent of the immune pathways active in the disease that we examined in this study.

Identifiants

pubmed: 30997535
doi: 10.1007/s00262-019-02340-w
pii: 10.1007/s00262-019-02340-w
doi:

Substances chimiques

Antigens, CD 0
B7-H1 Antigen 0
Biomarkers, Tumor 0
CD274 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

991-997

Auteurs

Bradley C Holland (BC)

Department of Surgery, Division of Urology, Southern Illinois University School of Medicine, Springfield, IL, USA.

Akshay Sood (A)

VCORE-Center for Outcomes Research, Analytics, and Evaluation, Vattikuti Urology Institute, Henry Ford Hospital, 2799 W. Grand Boulevard, Detroit, MI, 48202, USA.

Kristin Delfino (K)

Department of Surgery, Division of Urology, Southern Illinois University School of Medicine, Springfield, IL, USA.

Danuta I Dynda (DI)

Department of Surgery, Division of Urology, Southern Illinois University School of Medicine, Springfield, IL, USA.

Sophia Ran (S)

Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Springfield, IL, USA.

Natalie Freed (N)

Pathology Associates of Central Illinois, Springfield, IL, USA.

Shaheen Alanee (S)

Department of Surgery, Division of Urology, Southern Illinois University School of Medicine, Springfield, IL, USA. salanee1@hfhs.org.
VCORE-Center for Outcomes Research, Analytics, and Evaluation, Vattikuti Urology Institute, Henry Ford Hospital, 2799 W. Grand Boulevard, Detroit, MI, 48202, USA. salanee1@hfhs.org.

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Classifications MeSH