Bladder Cancer Clinical Trial
Official title:
Chemoresection With 4 Weekly Intravesical Instillations Of Mitomycin C Versus Transurethral Resection (TUR) Followed By One Single Immediate Instillation Of Mitomycin C In Single, Small, Papillary Stage Ta, T1 Bladder Tumors: A Prospective Randomized Phase III Trial
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing
so they stop growing or die. Infusing chemotherapy drugs directly into the bladder may kill
more cancer cells. It is not yet known if surgery followed by chemotherapy is more effective
than chemotherapy alone in treating bladder cancer.
PURPOSE: Randomized phase III trial to compare the effectiveness of chemotherapy alone with
that of transurethral resection followed by chemotherapy in treating patients who have
bladder cancer.
OBJECTIVES:
- Compare the efficacy of chemoresection with 4 weekly intravesical instillations of
mitomycin vs transurethral resection followed by 1 instillation of mitomycin in
patients with low-risk superficial transitional cell carcinoma of the bladder.
- Compare the disease-free survival of patients treated with these regimens.
- Determine the response rate at 6 weeks in patients treated with chemoresection.
- Determine the percent of patients with tumor at 6 weeks treated with transurethral
resection.
- Compare the quality of life of patients treated with these regimens.
- Compare the side effects of these regimens in these patients.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to
disease status (primary vs recurrent) and participating center. Patients are randomized to 1
of 2 treatment arms.
- Arm I: Patients undergo chemoresection with intravesical instillation of mitomycin once
weekly for 4 weeks.
- Arm II: Patients undergo transurethral resection followed within 1-6 hours by
intravesical instillation of mitomycin.
Quality of life is assessed at baseline, at week 1 (arm II only), at week 5 (arm I only),
and then at week 6.
Patients are followed at weeks 6 and 19, every 6 months for 3 years, and then annually for 2
years.
PROJECTED ACCRUAL: A total of 1,000 patients (500 per treatment arm) will be accrued for
this study within 5 years.
;
Allocation: Randomized, Primary Purpose: Treatment
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