SWOG clinical trial number
S0306
Phase II Study of Irinotecan in Patients with Advanced Transitional Cell Carcinoma of the Urothelium
Closed
Phase
Accrual
100%
Published
Abbreviated Title
Advanced Bladder
Activated
07/15/2003
Closed
02/01/2007
Participants
Research committees
Genitourinary Cancer
Treatment
Irinotecan
Eligibility Criteria Expand/Collapse
Pts must have histo conf T2-4, N0-3, M1 TCC of the urothelial tract not curable by surgery or RT. Stage T2-4, N+, M0 pts w/unresectable disease are also eligible. Pts must have mx disease. Pts must have disease that progressed or recurred after one and only one cisplatin or carboplatin containing regimen for metastatic disease. Pts must not have rec'd prior tx w/ a topoisomerase I inhibitor such as irinotecan or topotecan. Pts may have rec'd prior RT to the pelvis. Pts must have AGC >/= 1,200; PLT >/= 100,000; bili < 1.5 x IULN, SGOT < 3 x IULN, & CREAT < 2 .x IULN w/in 28 days prior to registration. Pts must have stopped taking St. John's Wort at least 14 days prior to registration & must not be planning to take it while on protocol tx and for 7 days following completion of protocol tx. Pts must not have rec'd phenytoin, phenobarbital, carbamazepine or any other enzyme-inducing anti-convulsant drug w/in 7 days prior to registration. Pt must have a Zubrod PS of 0-2. Pts must have no uncontrolled CNS mets. Pts must not be pregnant or nursing. Pts of reproductive potential must have agreed to use an effective contraceptive method.
Publication Information Expand/Collapse
2013
2008
Southwest Oncology Group phase II study of irinotecan in patients with advanced transitional cell carcinoma of the urothelium [PMID18501081]
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