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Sociodemographic and survival disparities for histologic variants of bladder cancer

Joshua S. Jue1,2, Tulay Koru-Sengul3,4, Kevin J. Moore2,3, Feng Miao2, Mahmoud Alameddine1, Bruno Nahar1, Sanoj Punnen1, Dipen J. Parekh1,4, Chad R. Ritch1, Mark L. Gonzalgo1,4

1 Department of Urology, University of Miami Miller School of Medicine, Miami, Florida, USA
2 Medical Education, University of Miami Miller School of Medicine, Miami, Florida, USA
3 Department of Public Health Sciences, University of Miami Miller School of Medicine, Miami, Florida, USA
4 Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida, USA
Address correspondence to Dr. Mark L. Gonzalgo, Department of Urology, University of Miami – Miller School of Medicine, 1120 NW 14th Street, Suite 1560, Miami, FL 33136 USA

Canadian Journal of Urology 2018, 25(1), 9179-9185.

Abstract

Introduction: To investigate the impact of perioperative factors on overall survival among patients with histologic variants of bladder cancer treated with radical cystectomy.
Materials and methods: The National Cancer Data Base (NCDB) was utilized to identify patients diagnosed with muscle-invasive bladder cancer (cT2–T4, N0, M0) from 2004 to 2013. Variant histology bladder cancers—including non-mucinous adenocarcinoma, mucinous/signet ring adenocarcinoma, micropapillary urothelial carcinoma, small cell carcinoma, and squamous cell carcinoma—were compared to urothelial carcinoma with respect to overall survival. Adjusted hazard ratios (aHR) and 95% confidence intervals (CI) were calculated using a multivariable Cox regression model to examine factors affecting overall survival, T upstaging, N upstaging, and positive surgical margins. Median survival was estimated using Kaplan-Meier analysis.
Results: A total of 5,856 patients were included in this study. Significant predictors of worse overall survival included African-American ancestry (aHR = 1.24, 95% CI: 1.03–1.48, p = 0.021), age (aHR = 1.03, 95% CI: 1.02–1.03, p < 0.001), comorbidity (aHR = 1.30, 95% CI: 1.20–1.40, p < 0.001), clinical T3 stage (aHR = 1.41, 95% CI: 1.26–1.57, p < 0.001), and clinical T4 stage (aHR = 1.59, 95% CI: 1.38–1.84, p < 0.001). Small cell carcinoma (aHR = 2.10, 95% CI: 1.44–3.06, p < 0.001) and non-mucinous adenocarcinoma (aHR = 1.59, 95% CI: 1.15–2.20, p = 0.005) were significant predictors of worse overall survival compared to urothelial carcinoma. Small cell carcinoma had the worst 5-year overall survival rate (15.5%, 95% CI: 5.2%–30.9%), compared to urothelial carcinoma (48.7%, 95% CI: 47.2%–50.2%). Micropapillary urothelial carcinoma was significantly associated with increased risk of nodal positivity and positive surgical margins after radical cystectomy compared to urothelial carcinoma (aHR = 6.01, 95% CI: 3.11–11.63, p < 0.001; aHR = 4.38, 95% CI: 2.05–9.38, p < 0.001).
Conclusions: Among bladder cancer patients with equal treatment and staging, small cell carcinoma and non-mucinous adenocarcinoma variant histologies were associated with worse overall survival compared to urothelial carcinoma. Patient demographic factors such as African-American ancestry and older age were also independent predictors of poorer survival outcomes in both variant histology bladder cancer and urothelial carcinoma.

Keywords

bladder cancer, histology, histologic variants, sociodemographic disparities, National Cancer Data Base, NCDB

Cite This Article

APA Style
Jue, J.S., Koru-Sengul, T., Moore, K.J., Miao, F., Alameddine, M. et al. (2018). Sociodemographic and survival disparities for histologic variants of bladder cancer. Canadian Journal of Urology, 25(1), 9179–9185.
Vancouver Style
Jue JS, Koru-Sengul T, Moore KJ, Miao F, Alameddine M, Nahar B, et al. Sociodemographic and survival disparities for histologic variants of bladder cancer. Can J Urology. 2018;25(1):9179–9185.
IEEE Style
J.S. Jue et al., “Sociodemographic and survival disparities for histologic variants of bladder cancer,” Can. J. Urology, vol. 25, no. 1, pp. 9179–9185, 2018.



cc Copyright © 2018 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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