Finding studies
Finding studies
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Lead
Robert Morris
With
OBJECTIVES: Primary * Determine the response rate in patients with platinum-sensitive or -resistant relapsed or refractory ovarian epithelial or peritoneal cavity cancer treated with gemcitabine and docetaxel. Secondary * Determine the toxicity of this regimen in these patients. * Determine the overall survival of patients treated with this regimen. * Determine the time to treatment failure and progression-free survival of patients treated with this regimen. OUTLINE: This is a multicenter study. Patients are stratified according to response to prior treatment with a platinum-containing regimen (platinum-resistant disease vs platinum-sensitive disease). Patients receive gemcitabine IV over 30 minutes and docetaxel IV over 30 minutes on days 1 and 8. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients achieving a complete response (CR) receive 3 additional courses beyond CR (≥ 6 total courses of treatment). PROJECTED ACCRUAL: Approximately 36-62 patients (19-29 for stratum I \[platinum-resistant disease\] and 17-33 for stratum II \[platinum-sensitive disease\]) will be accrued for this study.
Age
18–120
Sex
FEMALE
Healthy volunteers
Not accepted
