Clinical Trials Directory

Trials / Completed

CompletedNCT00087035

Docetaxel and Erlotinib in Treating Older Patients With Prostate Cancer

Phase II Trial Of TAXOTERE + TARCEVA™ To Treat HRPC In Men ≥ 65 Years Of Age

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
1 (actual)
Sponsor
Jonsson Comprehensive Cancer Center · Academic / Other
Sex
Male
Age
65 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop tumor cells from dividing so they stop growing or die. Erlotinib may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Combining docetaxel with erlotinib may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving docetaxel together with erlotinib works in treating older patients with progressive prostate cancer that has not responded to hormone therapy.

Detailed description

OBJECTIVES: Primary * Determine the response rate and response duration in older patients with progressive hormone refractory prostate cancer treated with docetaxel and erlotinib. Secondary * Determine the safety of this regimen in these patients. * Evaluate the quality of life of patients treated with this regimen. OUTLINE: This is a multicenter study. * Initial combination therapy: Patients receive docetaxel IV over 1 hour on day 1 and oral erlotinib once daily on days 1-21. Treatment repeats every 21 days for up to 9 courses in the absence of disease progression or unacceptable toxicity. Patients with responding disease receive 3 additional courses beyond maximal response. * Extension phase: After 9 courses of initial combination therapy, patients achieving a complete response, partial response, or stable disease receive 8 courses of erlotinib alone (total of 17 courses of study treatment). Quality of life is assessed at baseline, day 1 of each course, and at the end of study treatment. For patients in the extension phase, quality of life is also assessed on day 1 of courses 10, 12, 14, and 16. Patients are followed every 3 months. PROJECTED ACCRUAL: A total of 22 patients will be accrued for this study within 24 months.

Conditions

Interventions

TypeNameDescription
DRUGdocetaxelAdministered as an IV infusion of 60m/m2 over a 1-hour period, once every 21 ± 2 days
DRUGerlotinib hydrochlorideWill be taken at a starting daily dose of 150mg

Timeline

Start date
2004-05-01
Primary completion
2006-06-01
Completion
2008-03-01
First posted
2004-07-12
Last updated
2020-08-03

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00087035. Inclusion in this directory is not an endorsement.