Clinical Trials Directory

Trials / Terminated

TerminatedNCT00459810

Paclitaxel Poliglumex and Estradiol in Treating Patients With Stage IV Prostate Cancer

A Phase II Study of Paclitaxel Poliglumex (PPX) in Combination With Transdermal Estradiol for the Treatment of Androgen Independent Prostate Cancer After Docetaxel Chemotherapy

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
21 (actual)
Sponsor
OHSU Knight Cancer Institute · Academic / Other
Sex
Male
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy, such as paclitaxel poliglumex, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Estradiol may kill prostate cancer cells that no longer respond to hormone therapy. Giving paclitaxel poliglumex together with estradiol may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving paclitaxel poliglumex together with estradiol works in treating patients with stage IV prostate cancer.

Detailed description

OBJECTIVES: Primary * Determine the PSA response rate in patients with androgen independent metastatic prostate cancer treated with paclitaxel poliglumex and transdermal estradiol. Secondary * Determine the toxicity of this regimen in these patients. * Determine the response rate in patients treated with this regimen. * Determine the time to PSA progression and measurable disease progression in patients treated with this regimen. * Determine time to death from all causes in patients treated with this regimen. * Correlate levels of serum estradiol, serum cathepsin B, and bone turnover markers with PSA response in patients treated with this regimen. OUTLINE: This is a multicenter study. Patients receive transdermal estradiol continuously (patches changed every 7 days) until the PSA level rises. Patients whose PSA increases above baseline or PSA decreases \< 10% after 4 weeks of estradiol therapy or whose serum PSA reduction is \< 50% after 12 weeks of estradiol therapy also receive paclitaxel poliglumex therapy. These patients receive paclitaxel poliglumex IV over 10-20 minutes on day 1. Treatment with paclitaxel poliglumex repeats every 28 days for up to 10 courses in the absence of disease progression or unacceptable toxicity. After completion of study therapy, patients are followed every 6 months. PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGtransdermal estradiolTransdermal estradiol given 0.2mg/day for duration of study.
DRUGpaclitaxel poliglumexPaclitaxel poliglumex (PPX) is a macromolecular polymer-drug conjugate of paclitaxel. PPX was given every 28 days, at a dose of 150 mg/m2

Timeline

Start date
2007-02-01
Primary completion
2009-07-01
Completion
2009-07-01
First posted
2007-04-13
Last updated
2017-04-28
Results posted
2010-06-23

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00459810. Inclusion in this directory is not an endorsement.