Overview

Standard Chemotherapy Compared With High-Dose Combination Chemotherapy and Peripheral Stem Cell Transplantation in Treating Women With Breast Cancer

Status:
Completed
Trial end date:
1999-06-01
Target enrollment:
0
Participant gender:
Female
Summary
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 allow doctors to give higher doses of chemotherapy drugs and kill more tumor cells. It is not yet known which treatment regimen is more effective for breast cancer. PURPOSE: Randomized phase III trial to compare the effectiveness of standard cyclophosphamide, methotrexate, and fluorouracil with that of high-dose combination chemotherapy plus peripheral stem cell transplantation in treating women who have stage II or stage IIIA breast cancer.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Scottish Cancer Therapy Network
Treatments:
Cobalt
Cyclophosphamide
Doxorubicin
Fluorouracil
Liposomal doxorubicin
Methotrexate
Tamoxifen
Thiotepa
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed stage II or IIIA breast cancer with at
least 4 positive axillary nodes Definitive resection required, preferably within 4 weeks
prior to entry No overt residual axillary nodal carcinoma after surgery Hormone receptor
status: Not specified

PATIENT CHARACTERISTICS: Age: Over 18 Sex: Female Menopausal status: Not specified
Performance status: ECOG 0 or 1 Hematopoietic: Absolute neutrophil count greater than
1,500/mm3 Platelet count greater than 100,000/mm3 Hemoglobin greater than 9 g/dL PT and
aPTT normal Hepatic: Bilirubin normal (unless benign congenital hyperbilirubinemia) Normal
liver biopsy required in patients with active hepatitis B or C Renal: Creatinine normal
Cardiovascular: No active heart disease Normal wall motion on MUGA or echocardiogram Other:
Adequate nutritional status (i.e., more than 1,000 calories/day orally) HIV negative No
serious medical or psychiatric disease No second malignancy except: Basal cell skin cancer
Carinoma in situ of the cervix Not pregnant Negative pregnancy test

PRIOR CONCURRENT THERAPY: At least 2 weeks since major surgery