Clinical Trials Directory

Trials / Unknown

UnknownNCT00006120

Docetaxel or Paclitaxel in Treating Women With Unresectable Locally Advanced or Metastatic Breast Cancer

Phase II Randomized Study of Two Different Schedules of Docetaxel or Paclitaxel for Metastatic Breast Cancer

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group · Academic / Other
Sex
Female
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Randomized phase II trial to compare the effectiveness of two different regimens of docetaxel or paclitaxel in treating women who have unresectable locally advanced or metastatic breast cancer.

Detailed description

OBJECTIVES: * Compare the response rate, progression free survival, and overall survival in women with unresectable locally advanced or metastatic breast cancer treated with two different schedules of docetaxel or paclitaxel. * Compare the toxicities and pharmacoeconomics of these four regimens in these patients. * Compare the quality of life of patients treated with these four regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified by center, age, ECOG performance status, hormone receptor status (positive vs negative), metastasis to liver (yes vs no), and presence of disease progression following anthracyclines (yes vs no). Patients are randomized to one of four treatment arms. * Arm I: Patients receive docetaxel IV over 1 hour on day 1. * Arm II: Patients receive paclitaxel IV over 3 hours on day 1. * Arm III: Patients receive docetaxel IV over 1 hour on days 1, 8, 15, 22, 29, and 36. * Arm IV: Patients receive paclitaxel IV over 1 hour on days 1, 8, 15, 22, 29, and 36. Courses repeat every 3 weeks (arms I and II) or every 8 weeks (arms III and IV) in the absence of disease progression or unacceptable toxicity. Quality of life is assessed prior to treatment and then every 8 weeks. PROJECTED ACCRUAL: A total of 165 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGdocetaxel
DRUGpaclitaxel

Timeline

Start date
2000-05-01
First posted
2003-01-27
Last updated
2008-07-24

Locations

35 sites across 2 countries: France, Luxembourg

Source: ClinicalTrials.gov record NCT00006120. Inclusion in this directory is not an endorsement.