Clinical Trials Directory

Trials / Completed

CompletedNCT00004001

S9916, Combination Therapy in Treating Patients With Advanced Prostate Cancer That Has Not Responded to Hormone Therapy

Docetaxel and Estramustine Versus Mitoxantrone and Prednisone for Advanced, Hormone Refractory Prostate Cancer

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
770 (actual)
Sponsor
SWOG Cancer Research Network · Network
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy and hormone therapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug and giving drugs in different ways may kill more tumor cells. It is not yet known whether estramustine plus docetaxel is more effective than mitoxantrone plus prednisone for prostate cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of estramustine plus docetaxel with that of mitoxantrone plus prednisone in treating patients who have stage IV prostate cancer that has not responded to hormone therapy.

Detailed description

OBJECTIVES: * Compare the overall survival and progression-free survival in patients with hormone-refractory, metastatic adenocarcinoma of the prostate treated with docetaxel and estramustine vs mitoxantrone and prednisone. * Compare the qualitative and quantitative toxic effects of these regimens in this patient population. * Compare the quality of life, including palliation of metastatic bone pain and global quality of life, of patients treated with these regimens. * Record prostate-specific antigen values for future correlations with response and survival in patients treated with these regimens. * Compare the responses in patients with bidimensionally measurable disease treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to disease status (measurable or evaluable disease progression vs rising PSA only), NCI Common Toxicity Criteria version 2.X pain scale (grade 2 or greater vs less than 2), and SWOG performance status (0-1 vs 2-3). Patients are randomized to one of two treatment arms. * Arm I: Patients receive oral estramustine 3 times daily on days 1-5 and docetaxel IV over 1 hour on day 2. * Arm II: Patients receive mitoxantrone IV over 30 minutes on day 1 and oral prednisone twice daily on days 1-21. Treatment in both arms repeats every 3 weeks for a maximum of 12 courses in the absence of unacceptable toxicity or disease progression. Quality of life is assessed at baseline, after courses 4 and 8, and then at 1 year after randomization. Patients are followed every 6 months for 2 years and then annually for 1 year. PROJECTED ACCRUAL: A total of 620 patients (310 per arm) will be accrued for this study within 3.5 years.

Conditions

Interventions

TypeNameDescription
DRUGdocetaxel
DRUGestramustine
DRUGmitoxantrone
DRUGprednisone

Timeline

Start date
1999-10-01
Primary completion
2006-07-01
Completion
2007-01-01
First posted
2003-01-27
Last updated
2014-02-25

Locations

16 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00004001. Inclusion in this directory is not an endorsement.