Intravenous Estramustine With Taxol in Hormone Refractory Prostate Adenocarcinoma

NCT ID: NCT00038168

Last Updated: 2012-08-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2000-06-30
• Study Completion Date: 2003-01-31

Brief Summary

Phase I: The goal of this clinical research study is to find the highest dose of estramustine phosphate administered intravenously in combination with a fixed dose of Taxol (paclitaxel) that can be given safely to participants with prostate cancer who have failed to further benefit from hormone treatment.

Phase II: The goal of this clinical research study is to find out if the combination of the drugs estramustine phosphate and paclitaxel will shrink or control prostate cancer that has not responded to hormone treatment. A second goal is to find out if the side effects of these drugs can be reversed. The safety of these drugs will also be studied.

Detailed Description

To determine the maximum tolerated dose of intravenous estramustine phosphate combined with Taxol.

To estimate the complete and partial response rates to treatments with intravenous estramustine phosphate combined with Taxol in the treatment of hormone-refractory adenocarcinoma of the prostate.

To determine the qualitative and quantitative toxicity of the combination of intravenous estramustine phosphate and Taxol.

Conditions

Prostate Cancer

Keywords

Prostate Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Estramustine + Taxol

Group Type: EXPERIMENTAL

Estramustine

Intervention Type: DRUG

Intravenous dose

Taxol

Intervention Type: DRUG

Intravenous dose

Interventions

Estramustine

Intravenous dose

Intervention Type: DRUG

Taxol

Intravenous dose

Intervention Type: DRUG

Other Intervention Names

Estramustine phosphate; Paclitaxel

Eligibility Criteria

Inclusion Criteria

• Patients with histologic proof of adenocarcinoma of the prostate and must have failed conventional hormonal therapy.
• Patients must have osteoblastic bone metastases. At least one osteoblastic lesion must be documented by plain film. Patients with mixed or osteolytic bone metastases must have a biopsy to exclude histologic variants of prostate cancer or metastasis from another primary (for phase II only).
• Patients must have evidence of progression of disease as demonstrated by 2 consecutive rise in PSA (an absolute change of at least 1 ng/mL) over 4 weeks.
• Patients on flutamide, nilutamide, or bicalutamide should be discontinued from flutamide or nilutamide and bicalutamide for at least 4 weeks and 8 weeks, respectively.
• Patients must have an expected survival of at least three months and a Zubrod performance status of < 2 (Zubrod scale; Appendix B).
• Patients may receive no concurrent chemotherapy or immunotherapy.
• Patients must have castrate serum testosterone levels (< 30 ng/dl). For patients who are medically castrated, lutenizing hormone releasing hormone analog must continue to maintain testicular suppression.
• Patients must have adequate bone marrow function defined as an absolute peripheral granulocyte count of > 1,500/mm3 and platelet count of > 100,000/mm3; adequate hepatic function defined with a bilirubin of < 1.5 mg% and SGOT (AST) < 2X the upper limits of normal; adequate renal function defined as serum creatinine clearance > 40 cc/min (measured or calculated).
• Patients must be >= 18 years old.
• Patients may have received oral EMP or no more than one cytotoxic therapy.
• Patients must sign a written informed consent form prior to treatment.

Exclusion Criteria

• Patients with severe intercurrent infection.
• Patients with prior exposure to Taxol.
• Patients whose tumors contain small cell or sarcomatoid elements.
• Patients with evidence of conduction block or active myocardial ischemia on ECG.
• Patients with a history of prior malignancy (except noninvasive cutaneous carcinoma).
• Patients with a history of thromboembolism.

• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

M.D. Anderson Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jeri Kim, M.D.

Role: STUDY_CHAIR

UT MD Anderson Cancer Center

Locations

MD Anderson Cancer Center

Houston, Texas, United States

Countries

United States

Other Identifiers

DM98-268

Identifier Type: -

Identifier Source: org_study_id