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Clinical Trials/NCT06235853
NCT06235853
Completed
Not Applicable

Biomarkers of Recurrence and Progression in Non-muscle Invasive Bladder Cancer - an Association With Inflammatory Response and Plasminogen Activation System

Wroclaw Medical University1 site in 1 country240 target enrollmentJanuary 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non-muscle Invasive Bladder Cancer
Sponsor
Wroclaw Medical University
Enrollment
240
Locations
1
Primary Endpoint
Tumour recurrence or progression
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Bladder cancer (BC) is one of the most common type of cancer globally. Due to its high incidence rate, high risk of recurrence and progression, and frequent cystoscopy surveillance, BC contributes to major healthcare costs across the world. The goal of this prospective study was to evaluate the prognostic value of novel non-muscle invasive bladder cancer (NMIBC) biomarkers for predicting disease recurrence or progression after radical transurethral resection of bladder tumour (TURBT). The data obtained from this study may help physicians identify patients who are at greater risk of NMIBC recurrence or progression and require close supervision.

Detailed Description

The aim of our prospective study was to determine the prognostic impact of the inflammatory response and indicators of nutritional status on recurrence and progression of non-muscle invasive bladder cancer (NMIBC) in patients undergoing transurethral resection of bladder tumour (TURBT). We evaluated six biomarkers, 3 in blood serum: soluble urokinase plasminogen activator receptor (sUPAR), plasminogen activator inhibitor-1 (PAI-1), interleukin 8 (IL-8) and 3 in urine: apolipoprotein E (APOE), vascular endothelial growth factor (VEGF), interleukin 8 (IL-8). Furthermore, following indicators of nutritional status were investigated: Glasgow Prognostic Score (GPS) and Modified Glasgow Prognostic Score (mGPS). The primary endpoint of this study was the recurrence or progression of NMIBC based on the histopathological or cystoscopic result. The study outcome was evaluated during the first surveillance cystoscopy, which was performed in time intervals indicated by European Association of Urology. Based on literature data and statistical assumptions we aimed to recruit 240 patients with NMIBC.

Registry
clinicaltrials.gov
Start Date
January 1, 2020
End Date
April 30, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Wroclaw Medical University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Signed informed consent form
  • Presence or suspicion of tumour in urinary bladder
  • Qualification for the first transurethral resection of bladder tumour

Exclusion Criteria

  • age \< 18 years
  • active urinary tract infection
  • active autoimmune disease
  • end-stage renal failure and renal replacement therapy
  • active hepatitis A, B or C
  • active HIV infection
  • factors disqualifying the patient from adjuvant treatment (intravesical immunotherapy or intravesical chemotherapy)
  • bladder tumour stage T2 or more, or urothelial tumour in a location other than the urinary bladder
  • other cancer or systemic anticancer treatment carried out up to 5 years ago
  • factors disqualifying the patient from surgical treatment, e.g. coagulopathies

Outcomes

Primary Outcomes

Tumour recurrence or progression

Time Frame: Up to 1 year

Tumour recurrence or progression based on histopathological result from specimen from follow-up cystoscopy.

Study Sites (1)

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