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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)

NCT ID: NCT06310759Sponsor: Tampere University HospitalLast updated: 2025-10-10

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

Sex: AllAge: 18 Years to 100 YearsHealthy volunteers: No
Inclusion Criteria: * Willing and able to provide informed consent * Patient has been scheduled for cystoscopy to rule out urothelial cancer Exclusion Criteria: * Prior diagnosis of urothelial cancer (i.e. bladder cancer or upper tract urothelial carcinoma)

Study locations (1)

Jesse Brown Department Of Veterans Affairs Medical Center

Chicago, Illinois, 60612

Not Yet Recruiting
Joel Cornfield · Contact
Prospective Validation Study of High Volume Urine DNA Testing in Individuals With Suspicion of Urothelial Cancer | Cancerify