Overview

Capecitabine, Paclitaxel, and Trastuzumab in Treating Patients With Metastatic Breast Cancer

Status:
Completed
Trial end date:
2002-07-01
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Combining chemotherapy with monoclonal antibody therapy may kill more tumor cells. PURPOSE: Phase I/II trial to study the effectiveness of combining capecitabine, paclitaxel, and trastuzumab in treating patients who have metastatic breast cancer.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
UNC Lineberger Comprehensive Cancer Center
Collaborator:
National Cancer Institute (NCI)
Treatments:
Albumin-Bound Paclitaxel
Capecitabine
Paclitaxel
Trastuzumab
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the breast Metastatic
disease HER2 overexpressing tumor (2+ or 3+) Bidimensionally measurable or evaluable
disease Hormone receptor status: Estrogen receptor positive or negative

PATIENT CHARACTERISTICS: Age: 18 to 59 Menopausal status: Not specified Performance status:
ECOG 0-2 Life expectancy: Not specified Hematopoietic: Absolute granulocyte count at least
1,500/mm3 Platelet count at least 100,000/mm3 Hepatic: Bilirubin less than 1.5 times upper
limit of normal Renal: Creatinine less than 1.5 mg/dL Cardiovascular: Ejection fraction at
least 50% by MUGA No history of congestive heart failure No uncontrolled cardiac
arrhythmias Other: No other prior malignancy except squamous cell or basal cell carcinoma
of the skin, noninvasive ductal carcinoma of the breast, or cervical dysplasia No prior
motor or sensory neuropathy grade 2 or higher Not pregnant or nursing Negative pregnancy
test Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY: Biologic therapy: No prior trastuzumab (Herceptin) No concurrent
hematopoietic growth factors Chemotherapy: No prior chemotherapy for metastatic disease
Prior adjuvant chemotherapy allowed (including regimens containing doxorubicin) No prior
paclitaxel, 24 hour infusion fluorouracil, or capecitabine Endocrine therapy: Not specified
Radiotherapy: No prior radiotherapy to 50% or more of the bone marrow Surgery: Not
specified Other: No other concurrent experimental drugs