- St. John's Hospital
- Cancer Institute
Adult Clinical Trials: Bladder
RTOG 0233: BLADDER
A Phase II Randomized Trial For Patients With Muscle-Invading Bladder Cancer Evaluating Transurethral Surgery And BID Irradiation Plus Either Paclitaxel And Cisplatin Or 5-Fluorouracil And Cisplatin Followed By Selective Bladder Preservation And Gemcitabine/Paclitaxel/Cisplatin Adjuvant Chemotherapy
- Operable patients with muscularis propria invasion carcinoma of the bladder, all histologies; AJCC Stages T2-T4a, NX or N0, M0; No histologic evidence of tumor invasion into the stroma of the prostate
- No tumor-related hydronephrosis
- No node metastases
- Adequately functioning bladder; Patients must have undergone as thorough a transurethral resection of the bladder tumor as is judged safely possible
- Treatment must begin within 8 weeks following TUR
- Patients must be considered able to tolerate systemic chemotherapy, pelvic radiation therapy, and a radical cystectomy
- No prior systemic chemotherapy or pelvic RT
- No concurrent drugs that have potential nephrotoxicity or otoxicity
- No prior or concurrent malignancy (except stage T1a prostate cancer, carcinoma in situ of the uterine cervix, or non-melanoma skin cancer) unless disease free for > 5 years
Treatment
Induction Chemoradiotherapy starts within 8 weeks post TUR, Weeks 1-3:
Arm 1: paclitaxel, cisplatin, and BID irradiation
Arm 2: 5FU, cisplatin, and BID irradiation
Post-Induction Response Evaluation; Consolidation Chemoradiotherapy or Radical Cystectomy
Tumor Response; Consolidation Chemoradiotherapy, Weeks 8-9 for T0, Ta, Tcis:
Arm 1: paclitaxel, cisplatin, BID irradiation
Arm 2: 5FU, cisplatin, BID irradiation
For> T1: Radical Cystectomy, Week 9
Adjuvant Chemotherapy
