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Performance of Novel Non-Invasive Urine Assay Uroseek in Cohorts of Equivocal Urine Cytology Publisher Pubmed



Rodriguez Pena MDC1, 2 ; Springer SU3, 4 ; Taheri D2, 5 ; Li L3, 4 ; Tregnago AC2 ; Eich ML1, 2 ; Eltoum IEA1 ; Vandenbussche CJ2 ; Papadopoulos N3, 4 ; Kinzler KW3, 4 ; Vogelstein B3, 4 ; Netto GJ1, 2
Authors
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Authors Affiliations
  1. 1. Department of Pathology, The University of Alabama at Birmingham, Birmingham, 35233, AL, United States
  2. 2. Department of Pathology, The Johns Hopkins Hospital, Baltimore, 21231, MD, United States
  3. 3. The Ludwig Center for Cancer Genetics and Therapeutics, Baltimore, 21231, MD, United States
  4. 4. Sidney Kimmel Comprehensive Cancer Center, Baltimore, 21231, MD, United States
  5. 5. Department of Pathology, Isfahan Kidney Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Virchows Archiv Published:2020


Abstract

Urine cytology is an essential element of the diagnostic work up of hematuria. A significant proportion of cases continue to be placed in the “atypical” or “suspicious” categories of the Paris system for urine cytology, posing difficulty in patient management. We report on the performance of our recently described urine-based assay “UroSEEK” in cases with equivocal diagnosis in patients who are investigated for bladder cancer. Urine samples were collected from two cohorts. The first consisted of patients who presented with hematuria or lower urinary tract symptoms (early detection cohort) and the second of patients that are in follow-up for prior bladder cancer (surveillance cohort). Urine samples were analyzed for mutations in 11 genes and aneuploidy. In the early detection setting, we found high sensitivity and specificity (96% and 88%, respectively) and a strong negative predictive value of 99%. The assay performance was less robust in the surveillance cohort (sensitivity of 74%, specificity of 72%, and negative predictive value of 53%). UroSEEK demonstrated a notable lead time to cancer diagnosis. Seven cases in the early detection cohort and 71 surveillance cases were detected at least 6 months prior to clinical diagnosis. Our results suggest a potential role for UroSEEK assay in guiding management of patients with atypical urine cytology if confirmed in future prospective trials. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.
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