Overview

Docetaxel Followed by Radical Prostatectomy in Patients With High Risk Localized Prostate Cancer

Status:
Completed
Trial end date:
2011-05-01
Target enrollment:
0
Participant gender:
Male
Summary
The purpose of this research study is to determine if the combination of chemotherapy and hormone therapy is safe and helpful for patients who plan to have their high-risk prostate cancer surgically removed. Some physicians believe that patients with high risk cancer that is located in one area, may have an early but small spread of the cancer outside of the prostate, and perhaps even to distant organs. Therefore, better treatments for the entire body are needed to improve the ability of surgery or other local therapies to cure prostate cancer. Since chemotherapy is beginning to demonstrate increasing activity in advanced prostate cancer patients, it is possible that using chemotherapy combined with hormonal therapy earlier in the course of localized but high risk patients might improve the outcomes for these patients.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Beth Israel Deaconess Medical Center
Collaborator:
Walter Reed Army Medical Center
Treatments:
BB 1101
Bicalutamide
Dexamethasone
Dexamethasone 21-phosphate
Dexamethasone acetate
Docetaxel
Estramustine
Goserelin
Criteria
Inclusion Criteria:

- Histologically confirmed adenocarcinoma of the prostate

- Potential candidate for radical prostatectomy

- Any of the following: a) clinical stage T3 patients, b) Serum PSA greater than or
equal to 20 ng/ml, c) Gleason score 8-10, d) Clinical T2 disease and either MRI
evidence of seminal vesicle involvement or Gleason 4+3 cancer with either 5 or 6
biopsies positive

- ECOG Performance Status 0-1

- WBC > 3,000 ul

- HCT > 30%

- PLT > 100,000/ul

- LFTS within normal limits

Exclusion Criteria:

- Prior hormones, radiation or chemotherapy for prostate cancer

- Myocardial infarction within 1 year, significant change in anginal pattern within last
6 months, current congestive heart failure (NYHA Class 2 or higher), or deep venous
thrombosis within 1 year

- Evidence of active infection

- Significant peripheral neuropathy