Overview

This trial is active, not recruiting.

Condition breast cancer
Treatments cyclophosphamide, epirubicin hydrochloride, fluorouracil, methotrexate, laboratory biomarker analysis, adjuvant therapy
Phase phase 3
Sponsor Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori
Start date November 1997
End date December 2010
Trial size 800 participants
Trial identifier NCT01031030, CDR0000661068, IRST-IBIS-03

Summary

RATIONALE: Drugs used in chemotherapy, such as cyclophosphamide, methotrexate, fluorouracil, and epirubicin hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. It is not yet known whether giving cyclophosphamide together with methotrexate and fluorouracil before, after, or without epirubicin hydrochloride is more effective in treating patients with breast cancer that can be removed by surgery.

PURPOSE: This randomized phase III trial is comparing three regimens of cyclophosphamide given together with methotrexate and fluorouracil, with or without epirubicin hydrochloride, to see how well it works in treating women who have undergone surgery for breast cancer. (Group III was closed to new patients as of 12/7/2009.)

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Masking open label
Primary purpose treatment

Primary Outcomes

Measure
Overall survival
time frame:

Secondary Outcomes

Measure
Disease-free survival
time frame:
Toxicity
time frame:
Quality of life
time frame:
Efficacy in subgroups of patients
time frame:

Eligibility Criteria

Female participants from 18 years up to 70 years old.

DISEASE CHARACTERISTICS: - Histologically confirmed breast cancer - Underwent radical mastectomy, guadrantectomy, or tumorectomy with axillary node dissection within the past 4-6 weeks - Biologically aggressive disease - At least 10 lymph nodes removed - Node-negative (> 1 cm, or > 2 cm if histology is favorable, esp. tubular carcinoma and/or prevalent intraductal component > 50%) tumors OR node-positive (1-3) tumors, meeting the following criteria: - High thymidine-labeling index (> 3%) - Poorly differentiated tumor (grade III) - High S-phase fraction (> 10% by flow cytometry) - High Ki67/MIB1 expression (< 20%) - No bilateral breast cancer - No T4a, inoperable T4b, T4c, or T4d disease - Any estrogen receptor status (positive, negative, unknown) - No distant metastases PATIENT CHARACTERISTICS: - Any menopause status - WBC ≥ 3,500/mL - ANC ≥ 1,500/mL - Platelet count ≥ 120,000/mL - AST and ALT ≤ 1.5 times upper limit of normal (ULN) - Creatinine ≤ 1.5 mg/mL - Bilirubin ≤ 1.5 times ULN - Not pregnant - Geographically accessible for follow-up - No prior breast cancer and/or other cancer except for carcinoma in situ of the cervix or basal cell skin cancer treated with radical intent - No significant alterations in cardiovascular function - No serious psychiatric disorders - No impaired renal or liver function PRIOR CONCURRENT THERAPY: - See Disease Characteristics

Additional Information

Official title Adjuvant Treatment of Biologically Aggressive Breast Cancer (N-,N+1,3): Controlled Clinical Study
Principal investigator Dino Amadori, MD
Description OBJECTIVES: Primary - To determine the impact of adjuvant chemotherapy comprising epirubicin hydrochloride followed by cyclophosphamide, methotrexate, and fluorouracil versus cyclophosphamide, methotrexate, and fluorouracil followed by epirubicin hydrochloride versus cyclophosphamide, methotrexate, and fluorouracil on overall survival of patients with biologically aggressive, resectable, node-negative or node-positive breast cancer. Secondary - To assess the disease-free survival and patterns of relapse in these patients. - To assess the tolerance to and toxicity of treatment in these patients. - To determine the quality of life of these patients. - To verify the effectiveness of these treatments in different subgroups of patients. - To collect, retrospectively, information on the expression of tumor suppressor gene p53, oncogene c-erbB-2, and bcl-2 protein involved in apoptosis. (exploratory) OUTLINE: This is a multicenter study. Patients are stratified according to center, lymph node status (N0 vs N1-3), and estrogen receptor status (negative vs positive). Patients are randomized to 1 of 3 treatment arms. - Arm I: Beginning 4-6 weeks following surgery, patients receive epirubicin hydrochloride IV on day 1. Treatment repeats every 3 weeks for 4 courses. Patients then receive cyclophosphamide IV, methotrexate IV, and fluorouracil IV on days 1-8. Treatment repeats every 4 weeks for 4 courses. - Arm II: Beginning 4-6 weeks following surgery, patients receive cyclophosphamide IV, methotrexate IV, and fluorouracil IV on days 1-8. Treatment repeats every 4 weeks for 4 courses. Patients then receive epirubicin hydrochloride IV on day 1. Treatment repeats every 3 weeks for 4 courses. - Arm III (closed to accrual as of 12/7/2009): Beginning 4-6 weeks following surgery, patients receive cyclophosphamide IV, methotrexate IV, and fluorouracil IV on days 1-8. Treatment repeats every 4 weeks for 6 courses. Patients with estrogen receptor-positive disease receive tamoxifen daily for 5 years after completing chemotherapy. After completion of study therapy, patients are followed every 3 months for 1 year, every 6 months for 4 years, and then annually for 5 years.
Trial information was received from ClinicalTrials.gov and was last updated in August 2013.
Information provided to ClinicalTrials.gov by National Cancer Institute (NCI).