The goal of the Flemish Databank for Urothelial Cancer is to collect clinical and pathological data of patients treated for urothelial cancer (UC).
Eligibility
Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria:
* who are aged between 18-90,
* who are of male or female sex,
* who give their informed consent to collect their clinical and pathological data,
* who are planned to undergo TURBT for BC,
* who are planned to undergo (salvage) radical cystectomy with or without an extended pelvic lymph node dissection,
* who are planned to undergo tumor biopsy (from primary or metastatic tumor),
* who are planned to undergo radical nephroureterectomy ± partial cystectomy or segmental ureterectomy, with or without a lymph node dissection,
* who are planned to undergo endoscopic tumor biopsy or resection,
* from whom metastases will be surgically removed.
Exclusion Criteria:
* patients who do not give their informed consent to collect their clinical and pathological data,
* patients who withdraw their informed consent to use their clinical and pathological data,
* patients who refuse the planned treatment,
* women who are pregnant or have suspicion of pregnancy.
Primary outcome measure(s)
Progression to MIBC — 10 years Histopathologically proven muscle-invasive bladder cancer (at least T2 disease) in pathological evaluation of the TURBT specimen
Trial sites (1)
Facility
City
Region
Status
University Hospitals Leuven
Leuven
Vlaams-Brabant
Recruiting
More Universitaire Ziekenhuizen KU Leuven trials in Belgium
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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