SWOG clinical trial number
S9809

The Effect of Fluoroquinolones on the Disease-Free Interval in Patients with Stage Ta Transitional Cell Carcinoma of the Bladder, Phase III

Closed
Phase
Accrual
13%
Published
Abbreviated Title
Local Bladder
Activated
04/15/1999
Closed
07/01/2001
Participants
NCORP, Members, UCOP, Medical Oncologists, Surgeons

Research committees

Genitourinary Cancer

Treatment

Cephalexin Ciprofloxacin hydrochloride

Eligibility Criteria Expand/Collapse

Pts must have Stage Ta (any grade) transitional cell carcinoma of the bladder by cystoscopy (within 42 days). Pts w/ recurrent bladder disease must not have had a diagnosis greater than (or equal to) T2. Patients who are high risk for upper tract (ureter or renal/pelvic) transitional cell cancers are not eligible. Prior radiation therapy and/or intravesical therapy is allowed provided 28 days have elapsed and there are no toxicities. Pts must not be receiving hemo or peritoneal dialysis. Pts must not be allergic to fluoroquinolones. Pts must not be currently taking or have taken fluoroquinolone within 3 months of the cytoscopy. If pt allergic to penicillin or cephalosporin, pt must be able to take sulfamethoxazole/trimethoprim. Pts must not be currently taking probenecid or theophylline. All pts stratified as having recurrent disease must agree to submission of bladder washing samples (at time of TURBT).

Publication Information Expand/Collapse

2007

Aneusomy for detection of bladder cancer recurrence: a Southwest Oncology Group study [PMID17574960]

SR Wolman;B Goldman;ML Slovak;C Tangen;DL Persons;D Wood Cancer Genetics and Cytogenetics 176:22-27

2003

Southwest Oncology Group studies in bladder cancer

ED Crawford;DP Wood;DP Petrylak;J Scott;CA Coltman, Jr;D Raghavan Cancer Supplement 97(8):2099-2108

Other Clinical Trials

SWOG Clinical Trial Number
S2210

S2210, "Targeted Neoadjuvant Treatment for Patients with Localized Prostate Cancer and Germline DNA Repair Deficiency"

Research Committee(s)
Genitourinary Cancer
Activated
08/14/2023
Accrual
2%
Open
Phase
SWOG Clinical Trial Number
S2200
SWOG Clinical Trial Number
CTSU/A031901