Trastuzumab Plus Docetaxel in Treating Women With Recurrent or Metastatic Breast Cancer
- Conditions
- Breast Cancer
- Registration Number
- NCT00006104
- Lead Sponsor
- Vanderbilt-Ingram Cancer Center
- Brief Summary
RATIONALE: Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with monoclonal antibody therapy may kill more tumor cells.
PURPOSE: Phase II trial to study the effectiveness of trastuzumab plus docetaxel in treating women who have recurrent or metastatic breast cancer.
- Detailed Description
OBJECTIVES: I. Determine the objective response rate of women with HER2-neu overexpressing recurrent or metastatic breast cancer treated with trastuzumab (Herceptin) in combination with docetaxel. II. Determine the toxicity of this treatment regimen in these patients. III. Determine the duration of response to this treatment regimen in these patients. IV. Determine the time to progression in these patients after receiving this treatment regimen. V. Compare HER2-neu overexpression as determined by fluorescent in situ hybridization (FISH) versus immunohistochemistry, and correlate these findings with response to this treatment regimen in these patients. VI. Correlate HER2-neu activation by immunohistochemistry and the extracellular domain of HER2-neu by ELISA with response to this treatment regimen in these patients.
OUTLINE: This is a multicenter study. Patients receive docetaxel IV over 30 minutes weekly for 6 weeks plus trastuzumab (Herceptin) IV over 30-90 minutes weekly for 8 weeks. Treatment continues every 8 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed monthly for 3 months, every 3 months for 9 months, and then every 6 months thereafter.
PROJECTED ACCRUAL: A total of 18-34 patients will be accrued for this study.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 46
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (15)
Providence Hospital
🇺🇸Mobile, Alabama, United States
Robert H. Lurie Comprehensive Cancer Center, Northwestern University
🇺🇸Chicago, Illinois, United States
Evanston Hospital
🇺🇸Evanston, Illinois, United States
Owensboro Medical Health System
🇺🇸Owensboro, Kentucky, United States
Fox Chase Cancer Center
🇺🇸Philadelphia, Pennsylvania, United States
Erlanger Health Systems
🇺🇸Chattanooga, Tennessee, United States
Memorial Health Care System
🇺🇸Chattanooga, Tennessee, United States
Williamson Medical Center
🇺🇸Franklin, Tennessee, United States
Jackson-Madison County Hospital
🇺🇸Jackson, Tennessee, United States
Methodist/Thompson Oncology Research
🇺🇸Knoxville, Tennessee, United States
Scroll for more (5 remaining)Providence Hospital🇺🇸Mobile, Alabama, United States