Epirubicin and Tamoxifen With or Without Docetaxel in Treating Postmenopausal Women With Breast Cancer

Breast Cancer Clinical Trial

Official title:

A Multicenter Randomized Trial of Sequential Epirubicin and Docetaxel Versus Epirubicin in Node Positive Postmenopausal Breast Cancer Patients

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00010140
• Other study ID #: CDR0000068450
• Secondary ID: ICCG-C/14/96EU-2
• Status: Active, not recruiting
• Phase: Phase 3
• First received: February 2, 2001
• Last updated: December 17, 2013
• Start date: August 1997

Study information

• Verified date: September 2005
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

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

Study Design

Allocation: Randomized, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• docetaxel

• epirubicin hydrochloride

• tamoxifen citrate

Procedure:
• adjuvant therapy

Locations

Country	Name	City	State
United Kingdom	Charing Cross Hospital	London	England

Sponsors (1)

Lead Sponsor	Collaborator
International Collaborative Cancer Group

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Disease-free survival			No
Primary	Overall survival			No
Primary	Incidence of thromboembolic events during the first 9 months after randomization			No
Secondary	Tolerability			Yes
Secondary	Quality of life			No