Observational Prospective Multicenter Validation Study Investigating the Possibility of Replacing Cystoscopies With High Volume Urine DNA Testing in Individuals With Suspicion of Urothelial Cancer (UROSCOUT-1)
Summary
Urothelial cancers of the bladder and upper urinary tract account for over 200,000 deaths and 600,000 diagnoses annually worldwide. The most common presenting symptom is hematuria (blood in urine), triggering a cascade of tests, including an invasive examination of the bladder using a flexible scope (cystoscopy). Millions of cystoscopies are performed every year worldwide for patients presenting with hematuria, but only 10% result in a cancer diagnosis. The UROSCOUT-1 trial is a prospective multicenter observational study that explores the potential of urine tumor DNA (utDNA) testing to replace a significant portion of cystoscopies in the diagnostic setting for hematuria or other reasons to rule out urothelial cancer. The goal is to enhance patient quality of life, reduce healthcare costs, and address increased workloads in urology centers. Sample collection will be conducted by mail, and the samples will be analyzed in a blinded manner, without knowledge of which patients are diagnosed with cancer. Random subsampling will be applied to cancer-negative patients to achieve an approximate 1:1 ratio between cancer-positive and -negative patients.
Outcome measures
Primary
Sensitivity and specificity of urine tumor DNA (utDNA) test for urothelial cancer detection
Sensitivity and specificity of utDNA test for urothelial cancer detection, using histologically confirmed cancer diagnoses within 1 year of the diagnostic workup as ground truth
Time frame: 1 year after diagnostic workup
Secondary
Sensitivity and specificity of cystoscopy for urothelial cancer detection
Time frame: 1 year after diagnostic workup
Sensitivity and specificity of urine cytology for urothelial cancer detection
Time frame: 1 year after diagnostic workup
Time to diagnosis of urothelial cancer in patients with a positive utDNA test but negative cystoscopy
Time frame: 2, 5, and 10 years after diagnostic utDNA testing
Adverse event rate for cystoscopy
Time frame: 4 weeks after cystoscopy
Technical success rate of utDNA test
Time frame: Immediately after utDNA sample analysis
Estimate of diagnostic cystoscopies avoided
Time frame: 4 weeks after cystoscopy
Specificity of high-stringency utDNA threshold
Time frame: 1 year after diagnostic workup
Eligibility criteria
Study locations (1)
Jesse Brown Department Of Veterans Affairs Medical Center
Chicago, Illinois, 60612