Bladder Cancer Clinical Trial
S0353, Gemcitabine in Treating Patients With Recurrent Bladder Cancer That Has Not Responded to Previous Bacillus Calmette-Guerin
Summary
RATIONALE: Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving gemcitabine directly into the bladder may kill more tumor cells.
PURPOSE: This phase II trial is studying how well gemcitabine works in treating patients with recurrent bladder cancer that has progressed despite previous Bacillus Calmette-Guerin (BCG).
Full Description
OBJECTIVES:
Determine the 8-12 week efficacy of intravesical gemcitabine, in terms of complete response rate, in patients with recurrent superficial transitional cell carcinoma of the bladder that have progressed despite prior intravesical Bacillus Calmette-Guerin (BCG).
Determine the recurrence-free, worsening-free, progression-free, and overall survival of patients treated with this drug.
Evaluate the toxicity of this drug in these patients.
Correlate, preliminarily, expression levels of genes or genetic polymorphisms involved in the gemcitabine pathway and angiogenesis with clinical toxicity, response, and relapse-free survival of patients treated with this drug.
OUTLINE: This is a multicenter study.
Induction therapy: Patients receive gemcitabine intravesically once a week for 6 weeks (weeks 1-6) in the absence of disease progression or unacceptable toxicity. Patients achieving a complete response proceed to maintenance therapy at week 14.
Maintenance therapy: Patients receive gemcitabine intravesically once in weeks 14, 18, 22, 26, 30, 34, 38, 42, 46, and 50 in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed every 3 months for 2 years and then every 6 months for 3 years.
PROJECTED ACCRUAL: A total of 25-45 patients will be accrued for this study within 6-12 months.
Eligibility Criteria
DISEASE CHARACTERISTICS:
Histologically confirmed superficial transitional cell carcinoma (TCC) of the bladder meeting 1 of the following stage criteria:
Stage T1, grade 2-3
Stage Tis
Stage Ta, grade 3-4 or multifocal (> 2 lesions)
Must have received and failed ≥ 2 courses of intravesical Bacillus Calmette-Guerin (BCG) (one 6-week course, plus one 3-week course, or fewer weeks if BCG was discontinued due to side effects) within the past 3 years
Recurrent disease
Must have had a transurethral resection of the bladder tumor (TURBT) or bladder biopsy within the past 60 days documenting tumor recurrence and tumor stage and grade
TURBT or biopsy must have been performed ≥ 6 weeks after the completion of BCG and/or other immunotherapy treatment (or ≥ 14 days after completion of intravesical chemotherapy treatment)
All visible tumor must have been resected at the time of the last biopsy
No evidence of urethral or renal pelvis TCC by upper tract radiological imaging (e.g., intravenous pyelogram, CT urogram, or retrograde pyelogram) within the past 2 years
PATIENT CHARACTERISTICS:
Age
18 and over
Performance status
Zubrod 0-2
Life expectancy
Not specified
Hematopoietic
Not specified
Hepatic
Not specified
Renal
Not specified
Other
Not pregnant or nursing
Fertile patients must use effective contraception
No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or adequately treated stage I or II cancer that is in complete remission
PRIOR CONCURRENT THERAPY:
Biologic therapy
See Disease Characteristics
Prior intravesical interferon alfa allowed, alone or in combination with Bacillus Calmette-Guerin (BCG)
Chemotherapy
See Disease Characteristics
No more than 1 course of intravesical chemotherapy (e.g., thiotepa, mitomycin, or doxorubicin) within the past year, defined as 6 or more weekly instillations, with or without monthly maintenance instillations
No prior gemcitabine
Endocrine therapy
Not specified
Radiotherapy
No prior pelvic radiotherapy
No concurrent radiotherapy to any other area of the body
Surgery
See Disease Characteristics
Recovered from prior surgery
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There are 75 Locations for this study
Little Rock Arkansas, 72205, United States
Los Angeles California, 90089, United States
Leesburg Florida, 34788, United States
Aiea Hawaii, 96701, United States
Honolulu Hawaii, 96813, United States
Honolulu Hawaii, 96813, United States
Honolulu Hawaii, 96813, United States
Honolulu Hawaii, 96813, United States
Honolulu Hawaii, 96817, United States
Honolulu Hawaii, 96817, United States
Honolulu Hawaii, 96826, United States
Honolulu Hawaii, 96859, United States
Wailuku Hawaii, 96793, United States
Wailuku Hawaii, 96793, United States
Decatur Illinois, 62526, United States
Maywood Illinois, 60153, United States
Springfield Illinois, 62781, United States
Beech Grove Indiana, 46107, United States
Richmond Indiana, 47374, United States
Kansas City Kansas, 66160, United States
Olathe Kansas, 66061, United States
Shreveport Louisiana, 71105, United States
Shreveport Louisiana, 71130, United States
Ann Arbor Michigan, 48109, United States
Battle Creek Michigan, 49017, United States
Big Rapids Michigan, 49307, United States
Detroit Michigan, 48201, United States
Detroit Michigan, 48202, United States
Grand Rapids Michigan, 49503, United States
Grand Rapids Michigan, 49503, United States
Grand Rapids Michigan, 49503, United States
Muskegon Michigan, 49443, United States
Traverse City Michigan, 49684, United States
Wyoming Michigan, 49519, United States
Billings Montana, 59101, United States
Billings Montana, 59101, United States
Billings Montana, 59101, United States
Billings Montana, 59101, United States
Billings Montana, 59107, United States
Butte Montana, 59701, United States
Great Falls Montana, 59405, United States
Great Falls Montana, 59405, United States
Great Falls Montana, 59405, United States
Great Falls Montana, 59405, United States
Havre Montana, 59501, United States
Helena Montana, 59601, United States
Kalispell Montana, 59901, United States
Kalispell Montana, 59901, United States
Kalispell Montana, 59901, United States
Missoula Montana, 59801, United States
Missoula Montana, 59804, United States
Missoula Montana, 59807, United States
Missoula Montana, 59807, United States
Albuquerque New Mexico, 87131, United States
New York New York, 10032, United States
Rochester New York, 14642, United States
Goldsboro North Carolina, 27534, United States
Rutherfordton North Carolina, 28139, United States
Akron Ohio, 44307, United States
Dayton Ohio, 45405, United States
Dayton Ohio, 45406, United States
Dayton Ohio, 45409, United States
Dayton Ohio, 45415, United States
Dayton Ohio, 45428, United States
Dayton Ohio, 45429, United States
Findlay Ohio, 45840, United States
Franklin Ohio, 45005, United States
Greenville Ohio, 45331, United States
Kettering Ohio, 45429, United States
Troy Ohio, 45373, United States
Wilmington Ohio, 45177, United States
Xenia Ohio, 45385, United States
Coos Bay Oregon, 97420, United States
Portland Oregon, 97239, United States
Anderson South Carolina, 29621, United States
Spartanburg South Carolina, 29303, United States
Spartanburg South Carolina, 29303, United States
Knoxville Tennessee, 37920, United States
San Antonio Texas, 78209, United States
San Antonio Texas, 78229, United States
San Antonio Texas, 78229, United States
San Antonio Texas, 78229, United States
Temple Texas, 76508, United States
Salt Lake City Utah, 84112, United States
Martinsville Virginia, 24115, United States
Bellingham Washington, 98225, United States
Bremerton Washington, 98310, United States
Kennewick Washington, 99336, United States
Seattle Washington, 98104, United States
Seattle Washington, 98104, United States
Seattle Washington, 98104, United States
Seattle Washington, 98112, United States
Seattle Washington, 98122, United States
Seattle Washington, 98122, United States
Seattle Washington, 98195, United States
Spokane Washington, 99202, United States
Casper Wyoming, 82609, United States
Sheridan Wyoming, 82801, United States
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