Adenocarcinoma of the Prostate Clinical Trial
Official title:
A Phase II Study Of Estramustine, Docetaxel, And Bevacizumab (IND # 7921, NSC # 704865) In Men With Hormone Refractory Prostate Cancer
Phase II trial to study the effectiveness of combination chemotherapy plus monoclonal antibody therapy in treating patients who have metastatic prostate cancer that has not responded to previous hormone therapy. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies such as bevacizumab may stop the growth of cancer cells by stopping blood flow to the tumor. Combining monoclonal antibody therapy with chemotherapy may kill more tumor cells.
PRIMARY OBJECTIVES:
I. To determine time to objective progression, response rate (objective and PSA response)
and duration of response in men with hormone refractory prostate cancer treated with
estramustine, docetaxel and bevacizumab.
II. To determine the toxicity of this regimen in men with hormone refractory prostate
cancer.
III. To study the relationship of baseline VEGF levels in urine and plasma and changes in
these levels to response and duration of response to treatment with bevacizumab, docetaxel
and estramustine.
OUTLINE:
Patients receive oral estramustine 3 times daily on days 1-5 and docetaxel IV over 1 hour
followed by bevacizumab IV over 30-90 minutes on day 2. Treatment repeats every 21 days in
the absence of disease progression or unacceptable toxicity.
Patients are followed at least every 3 months for 2 years.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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