This trial is active, not recruiting.

Condition breast cancer
Treatments docetaxel, epirubicin hydrochloride, tamoxifen citrate, adjuvant therapy
Phase phase 3
Sponsor International Collaborative Cancer Group
Start date August 1997
Trial identifier NCT00010140, CDR0000068450, EU-20040, ICCG-C/14/96


RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Hormone therapy using tamoxifen may fight breast cancer by blocking the uptake of estrogen by the tumor cells. Combining chemotherapy with hormone therapy may kill more tumor cells.

PURPOSE: Randomized phase III trial to compare the effectiveness of epirubicin and tamoxifen with or without docetaxel in treating postmenopausal women who have breast cancer that has spread to the lymph nodes.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Allocation randomized
Primary purpose treatment

Primary Outcomes

Disease-free survival
time frame:
Overall survival
time frame:
Incidence of thromboembolic events during the first 9 months after randomization
time frame:

Secondary Outcomes

time frame:
Quality of life
time frame:

Eligibility Criteria

Female participants of any age.

DISEASE CHARACTERISTICS: - Histologically proven node-positive breast cancer - Postmenopausal - Last menstrual period more than 12 months before initial surgery OR - Any age with prior bilateral oophorectomy OR - Age 50 or over with prior hysterectomy without oophorectomy (unrelated to malignancy) - No distant metastases - Hormone receptor status: - Not specified PATIENT CHARACTERISTICS: Age: - See Disease Characteristics Sex: - Female Menopausal status: - See Disease Characteristics Performance status: - WHO (ECOG) 0-1 Life expectancy: - Not specified Hematopoietic: - WBC at least 3,000/mm3 OR - Absolute neutrophil count at least 1,500/mm3 - Platelet count at least 100,000/mm3 Hepatic: - Bilirubin normal - SGOT and SGPT no greater than 1.5 times normal - Alkaline phosphatase no greater than 1.5 times normal Renal: - Creatinine less than 1.5 times normal Cardiovascular: - No history of significant angina, congestive heart failure, or myocardial infarction within the past year - No clinically significant arrhythmias or uncontrolled hypertension - LVEF normal by MUGA, LV gated scan, or echocardiogram Other: - No other concurrent serious illness - No other prior or concurrent malignancy except adequately treated squamous cell or basal cell skin cancer or carcinoma in situ of the cervix PRIOR CONCURRENT THERAPY: Biologic therapy: - Not specified Chemotherapy: - Not specified Endocrine therapy: - Not specified Radiotherapy: - Not specified Surgery: - See Disease Characteristics

Additional Information

Official title A Multicenter Randomized Trial of Sequential Epirubicin and Docetaxel Versus Epirubicin in Node Positive Postmenopausal Breast Cancer Patients
Description OBJECTIVES: - Compare the impact of adjuvant epirubicin with or without docetaxel and concurrent or sequential tamoxifen on time to relapse and overall survival in postmenopausal women with node-positive breast cancer. - Compare the toxic effects of these regimens in this patient population. - Compare the quality of life in terms of shift in long term toxicity and differences in recuperation in women treated with these regimens. - Compare the incidence of thromboembolic events during the first 9 months of study and the influence of such events on compliance in women treated with these regimens. OUTLINE: This is a randomized, multicenter study. Patients are stratified according to participating center. Patients are randomized to one of two adjuvant chemotherapy treatment arms within 30 days after surgery. - Arm I: Patients receive adjuvant epirubicin IV on days 1 and 8. Treatment continues every 28 days for 6 courses. - Arm II: Patients receive adjuvant epirubicin IV on days 1 and 8. Treatment continues every 28 days for 3 courses. Patients then receive docetaxel IV over 1 hour on day 1. Treatment continues every 21 days for 3 courses. Patients may be further randomized to one of two tamoxifen arms. Patients not randomized to the tamoxifen arms receive oral tamoxifen daily for 5 years concurrently with adjuvant chemotherapy. - Arm I: Patients receive tamoxifen as above concurrently with adjuvant chemotherapy. - Arm II: Patients receive sequential tamoxifen as above after completion of adjuvant chemotherapy. Quality of life is assessed at baseline, 9 months, 2 years, and then at 5 years. Patients are followed at 9 months, 1 year, every 4 months for 1 year, every 6 months for 2 years, and then annually thereafter. PROJECTED ACCRUAL: A total of 800 patients will be accrued for this study.
Trial information was received from ClinicalTrials.gov and was last updated in December 2013.
Information provided to ClinicalTrials.gov by National Cancer Institute (NCI).