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Immunohistochemical Assessment of Basal and Luminal Markers in Non-Muscle Invasive Urothelial Carcinoma of Bladder Publisher Pubmed



Rodriguez Pena MDC1 ; Chaux A2 ; Eich ML1 ; Tregnago AC3 ; Taheri D4 ; Borhan W5 ; Sharma R3 ; Rezaei MK6 ; Netto GJ1, 3
Authors
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Authors Affiliations
  1. 1. Department of Pathology, The University of Alabama at Birmingham, WP Building, Suite P230, 619 19th Street South, Birmingham, 35249-7331, AL, United States
  2. 2. Department of Scientific Research, School of Postgraduate Studies, Norte University, Asuncion, Paraguay
  3. 3. Department of Pathology, Johns Hopkins University, Baltimore, 21287, MD, United States
  4. 4. Department of Pathology, Isfahan Kidney Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  5. 5. Department of Pathology, College of Medicine, Taibah University, Madinah, Saudi Arabia
  6. 6. Department of Pathology, George Washington University, Washington, 20037, DC, United States

Source: Virchows Archiv Published:2019


Abstract

The Cancer Genome Atlas project introduced genomic taxonomy of basal and luminal molecular subtypes in muscle invasive bladder cancer. Fewer studies have addressed the molecular classification in non-muscle invasive bladder cancer (NMIBC). Our aim is to assess the applicability of the proposed phenotypic classification for NMIBC. Three TMAs were constructed from 193 TURBT specimens of 60 bladder cancer patients treated at one of the authors’ institutions (1998–2008). Follow-up data on recurrence, grade, or stage progression was obtained. Immunohistochemistry was performed using an automated Ventana System for markers indicative of luminal (GATA3, CK20, ER, Uroplakin II, and HER2/neu) and basal (CK5/6 and CD44) phenotype. Marker expression was evaluated by 3 urologic pathologists. Using unadjusted logistic regression, we found significant association between tumor recurrence at next biopsy and CD44 expression (OR = 2.51, P = 0.03), tumor recurrence at any subsequent biopsy and ER expression (OR = 0.24, P = 0.04), and tumor grade progression at any subsequent biopsy and HER2/neu expression (OR = 0.24, P = 0.04). After adjusting for pathologic stage, we found a significant association between CK5/6 expression and tumor stage progression at either next or any subsequent biopsy (OR = 0.94, P = 0.006; and OR = 0.97, P = 0.02, respectively). Our findings suggest that individual immunohistochemical markers may be of value as prognostic factors in NMIBC. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.