SWOG clinical trial number
S0224

Phase II Study of Weekly Docetaxel in Patients with Advanced Epidermoid Carcinoma of the Penis

Closed
Phase
Accrual
5%
Abbreviated Title
Penile
Activated
10/15/2004
Closed
11/15/2005
Participants
NCORP, Members, UCOP, Medical Oncologists, Surgeons, ECOG

Research committees

Genitourinary Cancer

Treatment

Docetaxel

Eligibility Criteria Expand/Collapse

Pt must have bx proven epidermoid Ca of the penis w/distant mets (M1) or pathologically proven regional nodal mets (N1-3). Pt must have mx disease assessed w/in 28 days prior to reg. Pt may have rec'd prior RT, but at least 28 days must have elapsed. Pt must not have had any prior chemo for penile Ca. Pt must not have Gr 2 or greater peripheral neuropathy. Pt must not have hypersensitivity to drug formulated w/polysorbate-80. Pt must have AGC >/= 1500; PLT >/= 100,000; WBC >/= 3000 w/in 28 days prior to reg. Pt must have SGOT </= 2.5 x ULN and Alk Phos </= 4 X ULN and meet add'l criteria in Sect 5.8 of the protocol. Pt must have Zubrod P S </= 2.