This is a single arm Phase II study to explore the safety and efficacy of the combination of Taxotere and Herceptin in women with Her-2 overexpressing breast cancer who have received prior anthracycline therapy. Taxotere will be administered weeekly for three consecutive weeks with one week of rest, and Herceptin (loading dose of 4 mg/kg on week one followed by 2 mg/kg/weekly) will administered weekly. Response will be assessed after every 12 weeks of therapy. All patients will receive at least 16 weeks of therapy unless limited by toxicity and may continue on therapy until disease progression or undue toxicity is documented. All patients will be assessed for toxicity and adverse events weekly. Herceptin may be continued following best response on the combined regimen at the discretion of the investigator. Patients will be followed until progression or death is documented.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000054-39S3
Application #
6454278
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1999-12-01
Project End
2001-02-28
Budget Start
Budget End
Support Year
39
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Tufts University
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02111
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