The investigartors will conduct a randomized, multinational study with the aim to assess if the efficacy of a dose dense chemoablation with Mitomycin C (MMC) with adjuvant BCG in non-responding patients is superior regarding long term effect compared to standard treatment with trans urethral resection of bladder tumors (TURBT) and adjuvant intravesical instillation therapy in patients with recurrent Ta LG tumors. The study is a natural follow-up study following the pivotal NICSA trial supported by the Danish Cancer Society that has lead to the initial change in the European guidelines. In order to not only be comparable to current standard, but also to improve clinical outcome and furthermore confirm the previous findings, the investigators here suggest to implement at patient tailored approach through a new multicenter RCT. The investigators hypothesize that chemoablation with MMC in patients with recurrent Ta LG tumors will result in a permanent low recurrence rate in patients with complete response, whereas patients without complete response can be selected for adjuvant BCG which theoretically is more efficient in this select patient group. This will potentially result in a more favorable long term recurrence free survival (RFS) rate compared to the current standard regimen where all patients are treated with TURBT and adjuvant instillation therapy. The incidence of bladder cancer in Denmark is almost 2,000 per year. Of these, 75% have non-muscle invasive bladder cancer (NMIBC). The yearly recurrence rate of NMIBC is approximately 35% and the disease is therefore one of the most costly cancers to manage on a per patient basis, due to the cost of operative procedures, follow-up cystoscopies and instillation therapies
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
272
Chemoablation
Aalborg University Hospital
Aalborg, Denmark
NOT_YET_RECRUITINGAarhus University Hospital
Aarhus N, Denmark
RECRUITINGHerlev and Gentofte Hospital
Herlev, Denmark
RECRUITINGZealand University Hospital, Roskilde
Roskilde, Denmark
RECRUITINGLandspítali University Hospital
Reykjavik, Iceland
NOT_YET_RECRUITINGHaukeland University Hospital
Bergen, Norway
NOT_YET_RECRUITINGVestfold Hospital Trust
Tønsberg, Norway
NOT_YET_RECRUITINGNU Hospital Group
Uddevalla, Sweden
NOT_YET_RECRUITINGTwo-year Recurrence Free Survival
This is defined as event of first recurrence following treatment but not including the recurrence diagnosed at the time of inclusion or persisting tumour following chemoablation.
Time frame: 2 years
Five-year RFS
This is defined as event of first recurrence following treatment but not including the recurrence diagnosed at the time of inclusion or persisting tumour following chemoablation.
Time frame: 5 years
Number of patients in need of a TURBT or tumour fulguration in the outpatient clinic in the first two years following randomisation
need for TURBT/fulgaration
Time frame: 2 years
Number of tumours at first recurrence based on the following intervals: 1, 2-7, > 8
tumour number
Time frame: 5 years
Number of TURBTs per patient in the first two and five years of follow-up based on the following intervals: 1, 2-5, 5-10 and multiple
number of TURBTs
Time frame: 5 years
Five-year progression free survival
(progression defined as progression to T1-tumour, T2+-tumour, or cystectomy irrespectively of indication)
Time frame: 5 years
Five-year overall survival
survival
Time frame: 5 years
Number of patients completing assigned intervention
completing assigned intervention
Time frame: 2 years
Serious adverse events related to MMC treatment during neoadjuvant or adjuvant therapy
SAE's
Time frame: 2 years
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