Trial | NCT00023842  Report issue

Title

BCG With or Without Mitomycin in Treating Patients With Bladder Cancer
A Randomized Phase II Trial of Sequential Chemo-Immunotherapy Versus Immunotherapy Alone in Carcinoma in Situ of the Urinary Bladder

  • Phase

    Phase 2

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    97
RATIONALE: Biological therapies such as BCG use different ways to stimulate the immune system and stop tumor cells from growing. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with biological therapy may kill more tumor cells. It is not yet known if BCG is more effective with or without mitomycin.

PURPOSE: Randomized phase II trial to compare the effectiveness of BCG plus mitomycin with that of BCG alone in treating patients who have bladder cancer.
OBJECTIVES:

Compare the complete response rate of patients with carcinoma in situ of the bladder treated with adjuvant intravesical BCG with or without intravesical mitomycin following transurethral resection.
Compare the disease-free interval and type of recurrence after complete response in patients treated with these regimens.
Compare the side effects of these regimens in these patients.

OUTLINE: This is a randomized, open-label, multicenter study. Patients are randomized to one of two treatment arms.

Arm I:

Induction therapy: Patients receive intravesical mitomycin over 1 hour once weekly on weeks 1-6 and intravesical BCG once weekly on weeks 7-12. Patients with visible lesions or disease recurrence or progression undergo transurethral resection (TUR) during weeks 16-18 and receive one additional course of intravesical therapy.
Maintenance therapy:Patients with a complete response after either course of induction therapy proceed to maintenance therapy comprising intravesical mitomycin once on week 1 and intravesical BCG once weekly on weeks 2 and 3. Maintenance therapy repeats every 6 months through year 3.

Arm II:

Induction therapy:Patients receive intravesical BCG once weekly on weeks 1-6 and 10-12. Patients with visible lesions or disease recurrence or progression undergo transurethral resection (TUR) during weeks 16-18 and receive one additional course of intravesical therapy.
Maintenance therapy: Patients with a complete response after either course of induction therapy receive maintenance therapy comprising intravesical BCG once weekly on weeks 1-3. Maintenance therapy repeats every 6 months through year 3.

Patients are followed every 6 months for 5 years and then annually thereafter.

PROJECTED ACCRUAL: A total of 84-126 patients (42-63 per treatment arm) will be accrued for this study within 3.5 years.
Study Started
Jun 30
2001
Primary Completion
Feb 28
2005
Last Update
Sep 24
2012
Estimate

Biological BCG vaccine

Drug mitomycin C

Procedure adjuvant therapy

Procedure conventional surgery

Criteria 

DISEASE CHARACTERISTICS:

Histologically confirmed carcinoma in situ (CIS) of the bladder with urinary cytology

Primary CIS (no prior history of CIS, papillary, or solid transitional cell carcinoma [TCC] of the bladder and no concurrent papillary or solid TCC) OR
Secondary CIS (detected after complete resection of superficial Ta/T1 TCC of the bladder) OR
Concurrent CIS (in the presence of superficial primary or recurrent Ta/T1 TCC of the bladder)
No more than 28 days since prior transurethral resection (TUR) of all visible lesions
No muscle involvement
No prior or concurrent upper urinary tract tumors
No urethral strictures that would prevent endoscopic procedures and repeated catheterization
No upper urinary tract disease (e.g., vesico-ureteral reflux or massive stones) that would make multiple transurethral procedures risky

PATIENT CHARACTERISTICS:

Age:

Not specified

Performance status:

WHO 0-2

Life expectancy:

Not specified

Hematopoietic:

Not specified

Hepatic:

Not specified

Renal:

Not specified

Other:

Not pregnant or nursing
No active tuberculosis (highly positive skin tests allowed if no active disease)
No disease that would preclude general anesthesia
No active intractable or uncontrollable infection
No other prior or concurrent malignancy except cured basal cell skin cancer
No psychological, familial, sociological, or geographical condition that would preclude study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy:

No prior BCG

Chemotherapy:

More than 3 months since prior chemotherapy

Endocrine therapy:

Not specified

Radiotherapy:

No prior radiotherapy to the pelvis

Surgery:

See Disease Characteristics

Other:

More than 3 months since prior intravesical cytostatic agents
No Results Posted