Breast Cancer
Conditions
Keywords
stage I breast cancer
Brief summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. It is not yet known which combination chemotherapy regimen is more effective in treating early breast cancer. PURPOSE: Randomized phase III trial to determine the effectiveness of different regimens of combination chemotherapy in treating women who have stage I breast cancer.
Detailed description
OBJECTIVES: * Compare the efficacy of 4 vs 6 courses of adjuvant fluorouracil, epirubicin, and cyclophosphamide, in terms of 5-year survival, in women with stage I breast cancer. * Compare the toxicity of these regimens in these patients. * Determine the correlation of length of survival with biological factors in patients treated with these regimens. * Determine biological factors significant for prognosis and prediction of survival of patients treated with these regimens. * Determine the overall survival of patients treated with these regimens. OUTLINE: This is a randomized, open-label, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive fluorouracil IV, epirubicin IV, and cyclophosphamide IV on day 1. Treatment repeats every 3 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity. * Arm II: Patients receive the same regimen as in arm I for up to 4 courses. After completion of chemotherapy, patients undergo radiotherapy 5 days a week for 6 weeks. Patients who are estrogen or progesterone receptor positive also receive oral tamoxifen daily for 5 years, beginning after completion of chemotherapy. Patients are followed every 6 months for 5 years. PROJECTED ACCRUAL: A total of 1,512 patients (756 per treatment arm) will be accrued for this study within 3 years.
Interventions
DRUGcyclophosphamide
DRUGepirubicin hydrochloride
DRUGfluorouracil
Sponsors
UNICANCER
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically confirmed nonmetastatic, unilateral adenocarcinoma of the breast * Stage I * No clinically or radiologically suspicious metastases * No positive sentinel lymph nodes by immunohistochemistry for tumors less than 2 cm * No clinically proven positive axillary lymph nodes * Tumor cells found on immunohistochemistry only allowed * No clinically or radiologically contralateral suspicious lesions * No deeply adherent disease * No cutaneous invasion * No inflammatory disease * Complete surgical resection within the past 42 days * At least 8 lymph nodes removed * Tumor at least 1 cm with no residual disease * Presenting with at least 1 of the following factors of a poor prognosis: * Tumor greater than 2 cm * Hormone receptor negative tumor * Grade II or III * 35 years old or under * Hormone receptor status: * Positive or negative PATIENT CHARACTERISTICS: Age * 18 to 65 Sex * Female Menopausal status * Not specified Performance status * WHO 0-1 Life expectancy * Not specified Hematopoietic * WBC at least 2,000/mm\^3 * Platelet count at least 100,000/mm\^3 Hepatic * Bilirubin no greater than 1.25 times upper limit of normal (ULN) * AST and ALT no greater than 1.25 times ULN * Alkaline phosphatase no greater than 2.5 times ULN * No chronic hepatitis B * No active hepatitis C Renal * Creatinine no greater than 1.25 times ULN Pulmonary * FEV normal Other * Not pregnant or nursing * HIV negative * No prior breast cancer or other malignancy * No familial, social, or geographical reason that would preclude study participation PRIOR CONCURRENT THERAPY: Biologic therapy * Not specified Chemotherapy * No prior chemotherapy Endocrine therapy * No prior anticancer hormone therapy Radiotherapy * No prior radiotherapy Surgery * See Disease Characteristics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Efficacy, in terms of 5-year survival | 5 years from randomization |
Secondary
| Measure | Time frame |
|---|---|
| Event free survival | 5 years from randomization |
| Toxicity | 5 years from randomization |
| Biological factors significant for prognosis and prediction of survival | 5 years from randomization |
Countries
France
Outcome results
None listed