Prospective Study of Adjuvant Radiotherapy in High Risk Bladder Cancer. (Bladder-Aid)
Bladder Cancer
About this trial
This is an interventional treatment trial for Bladder Cancer
Eligibility Criteria
Inclusion Criteria:
- Age >18 years
- Karnofsky index > 60 % (ECOG < 2)
- Histologically confirmed muscle-invasive bladder cancer (MIBC) submitted to radical cystectomy.
- Pathological T-stage > pT3, and/or pathological N-stage > pN1, and/or residual tumor present after surgery (R>1)
- No distant metastases
- Written informed consent
Exclusion Criteria:
- Prior RT in the pelvic region
- Presence of distant metastases
- Pregnancy
- Inability to consent
Sites / Locations
- Istituto Clinico Humanitas
Arms of the Study
Arm 1
Experimental
Adiuvant Radiotherapy +/- CT
The radiation treatment will be delivered with two possible schedules, according to the presence of positive margins on the pathology specimen: R0: PTVb + PTVn 50 Gy in 25 fractions R1-2: PTVn 50 Gy in 25 fractions. PTVb (including cystectomy bed and residual tumor when present) 55 Gy in 25 fractions with simultaneous integrated boost (SIB). Considering an alfa/beta of 10 for bladder tumor and 3 for healthy tissues the equivalent doses will be respectively: BED10: 60/67.1; EQD2: 50/55.92 Gy BED3: 83.33/95.33; EQD2: 50/57.20 Gy Patients with ECOG PS<2, good haematological, hepatic and renal function (haemoglobin, neutrophil count, platelets, creatinine, glycaemia, Bilirubin, AST, ALT values within the limits of normal), will be submitted to concurrent cisplatin based weekly chemotherapy, 20-30 mg/m2, if they have not received neoadjuvant chemotherapy before surgery.