Finding studies
Finding studies
Take this into the appointment.
Saves the questions and what to expect into your notes, next to the visit they belong to.
Lead
OHSU Knight Cancer Institute
With
OBJECTIVES: * Determine the 5-year freedom from prostate-specific antigen (PSA) recurrence in patients treated with this regimen. * Define the maximum tolerated dose of neoadjuvant docetaxel and mitoxantrone followed by prostatectomy in patients with high-risk localized prostate cancer. (Phase I completed as of 2/15/02) * Determine the toxicity of this regimen in these patients. * Determine the PSA response rate and pathologic response rate in patients treated with this regimen. * Determine the clinical response in patients treated with this regimen. * Determine the overall survival of patients treated with this regimen. * Determine the surgical margin status at time of prostatectomy in patients treated with this regimen. OUTLINE: This is a dose-escalation study of mitoxantrone. (Phase I completed as of 2/15/02) Patients receive neoadjuvant docetaxel and mitoxantrone weekly on weeks 1-3. Treatment repeats once a week for a total of 4 courses. Patients receive escalating doses of mitoxantrone until the maximum tolerated dose is determined. (Phase I completed as of 2/15/02) Patients undergo prostatectomy 2-4 weeks after completion of neoadjuvant chemotherapy. PROJECTED ACCRUAL: A total of 60 patients will be accrued for this study.
Age
18–120
Sex
MALE
Healthy volunteers
Not accepted
