Overview

Fluorescence Cystoscopy and Optimized MMC in Recurrent Bladder Cancer (FinnBladder 9)

Status:
Unknown status
Trial end date:
2020-06-01
Target enrollment:
0
Participant gender:
All
Summary
Bladder cancer (BC), the second most common urological malignancy, is an important public health issue. One of the main challenges in the treatment of bladder cancer if the prevention of recurrences of non-invasive tumors, which is also associated with significant costs. The current study will investigate optimal treatment of patients with bladder cancer with high risk of tumor recurrence but low risk of progression. The main interest is comparison of photodynamic (PDD) bladder tumor resection (TUR-BR)to traditional TUR-BT. Also the efficacy of adjuvant optimized mitomycin-C is compared to patients with no adjuvant treatment.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Turku University Hospital
Collaborator:
Finnbladder
Treatments:
Mitomycin
Mitomycins
Criteria
Inclusion Criteria:

- Primary papillary bladder cancer at high risk for further recurrence as defined as
follows:

Number of primary tumors ≥2, OR Size of solitary primary tumor ≥ 3 cm, OR Recurrent
papillary tumors

- Histologically proven Ta bladder cancer

- Histological grade 1-2 (WHO 1973 grading system) or papillary urothelial neoplasm of
low malignant potential (PUNLMP) or low grade (WHO 2004 grading system) bladder cancer

- Written informed consent is required from every eligible patient

Exclusion Criteria:

- Grade 3 tumors (WHO 1973 grading system), or high grade tumors (WHO 2004 grading
system)

- CIS (carcinoma in situ)

- Suspicion or evidence of papillary tumors or CIS of the upper urinary tract

- Non-TCC (transitional cell carcinoma, i.e. urothelial carcinoma) bladder cancer

- Suspicion or previous history of the patient not tolerating intravesical instillations

- Known allergy to MMC or hexaminolevulinate (HAL, Hexvix®)

- Urethral stricture, stone disease, chronic urinary tract infection or any other
urological condition that may compromise study participation (as judged by treating
physician)

- Pregnancy or lactating patient

- Other non-cured malignancy (excepting skin basalioma or cancer in situ of the cervix
uteri or any other malignancy in remission ≥5 years)

- Age < 18 years

- Expected survival time less than one year

- Expected poor compliance (e.g. some severe psychiatric disorders, antisocial
behaviour, or dementia)