Prostate Cancer Clinical Trial
Official title:
A Phase II Study of Intravenous DX-8951f Administered Daily for Five Days Every Three Weeks to Patients With Hormone-Refractory Prostate Cancer
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing
so they stop growing or die.
PURPOSE: Phase II trial to study the effectiveness of DX-8951f in treating patients who have
metastatic prostate cancer that has not responded to hormone therapy.
OBJECTIVES: I. Determine the antitumor activity of DX-8951f as measured by PSA response in
patients with hormone refractory prostate cancer. II. Determine the antitumor activity of
this drug in the subpopulation of these patients with measurable disease. III. Evaluate the
quantitative and qualitative toxicities of this drug in these patients. IV. Evaluate the
pharmacokinetics of this drug in these patients.
OUTLINE: This is a multicenter study. Patients receive DX-8951f IV over 30 minutes daily for
5 days. Courses repeat every 21 days. Treatment continues in the absence of unacceptable
toxicity or disease progression. Patients with no evidence of PSA decrease by the start of
course 3 receive no further treatment. Patients are followed every 3 months until death.
PROJECTED ACCRUAL: A total of 12-37 patients will be accrued for this study.
;
Primary Purpose: Treatment
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