RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Peripheral stem cell transplantation may be able to replace immune cells that were destroyed by chemotherapy used to kill tumor cells, allowing higher doses of chemotherapy to be used.

PURPOSE: Phase I/II trial to study the effectiveness of paclitaxel when added to high-dose combination chemotherapy followed by peripheral stem cell transplantation in treating women with breast cancer at high risk of relapse.

OBJECTIVES: I. Estimate the maximum tolerated dose of paclitaxel when given with high-dose carboplatin/cyclophosphamide with autologous peripheral blood stem cell support in women with high-risk stage II/III breast cancer.

II. Assess the nonhematologic toxicities associated with this combination.

III. Assess the progression-free and overall survival of these patients following this treatment.

PROTOCOL OUTLINE: This is a dose-finding study. All patients undergo collection of peripheral blood stem cells (PBSC) with granulocyte colony-stimulating factor (G-CSF) mobilization prior to high-dose chemotherapy.

Cohorts of 3-5 patients are treated at successively higher dose levels of paclitaxel until a maximum tolerated dose (MTD) is found. Paclitaxel is given as a single 6-hour infusion, followed by fixed doses of high-dose cyclophosphamide for 2 days, then carboplatin for 3 days. Four days later, patients receive PBSC and G-CSF for hematopoietic reconstitution. Additional patients are entered at the MTD.

Patients are followed every 3 months for 1 year, every 4 months for 1 year, then every 4-6 months thereafter.

PROJECTED ACCRUAL: It is expected that 24-30 patients will be accrued; a study duration of 1-1.5 years is anticipated.

Ages Eligible for Study:  18 Years   -   65 Years

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

• Histologically diagnosed adenocarcinoma of the breast of the following stages: Stage II/IIIA disease with 4 or more involved axillary lymph nodes; Stage IIIB; Inflammatory
• No bone marrow involvement documented on bone marrow aspiration and biopsy
• Prior breast cancer allowed
• Hormone receptor status: Not specified

--Prior/Concurrent Therapy--

• At least 3 courses of induction therapy required, with regimen at the discretion of the investigator; No disease progression during induction

--Patient Characteristics--

• Age: 18 to 65
• Sex: Women only
• Menopausal status: Not specified
• Performance status: Karnofsky 70%-100%
• Hematopoietic: Not specified
• Hepatic: Bilirubin no greater than 2.0 mg/dL
• Renal: Creatinine clearance at least 60 mL/min
• Cardiovascular: Left ventricular ejection fraction at least 50% by MUGA; No abnormal cardiac conduction documented as second- or third-degree heart block or bundle branch block
• Pulmonary: DLCO at least 60% of predicted
• Other: Not HIV positive; No history of second malignancy within 5 years except: Nonmelanomatous skin cancer; In situ carcinoma of the cervix; No pregnant women