6xFU/Epirubicin/Cyclophosphamide (FEC) Compared to 3xFEC-3xDocetaxel in High-risk Node-negative Breast Cancer Patients (NNBC3-Europe)

Inclusion Criteria:

• Histological proven primary breast cancer
• Tumour size >0.5 cm and <5 cm (pT1b-pT2, pN0, M0)
• Axillary lymph nodes tumour free (node-negative disease)
• Adequate surgical procedure: R0-resection and axillary dissection with more than 10 lymph nodes examined or adequate sentinel procedure in a qualified centre
• Frozen tumour tissue available (for analysis of biological markers and microarrays, centres with biological risk assessment only). The material has to be stored in liquid nitrogen immediately after excision.
• Paraffin blocks or (at least) pathology slides of primary tumour (stained and unstained) and axillary nodes (stained) available for central review.
• HER-2/neu determination by immunohistochemistry. Patients will be stratified to be HER-2/neu-negative or HER-2/neu-positive (HER-2/neu Score 3+, or HER-2/neu Score 2+ and FISH positive).
• No distant metastasis
• Age >18 years, <70 years
• Performance status ECOG <2 (WHO Performance Status 0-1)
• Adequate cardiac function (echocardiographically measured left ventricular ejection fraction (LVEF) or shortening fraction (SF) within the normal limits, i.e. ≥55%)
• Adequate bone function (neutrophil count >1.5 x109 /l and platelet count >100 x109 /l)
• Adequate renal function (serum creatinine <120 µmol/l or 1.35 mg/dl) and hepatic function (serum bilirubin <1 x UNL, ASAT or ALAT (SGOT or SGPT) <2,5 x UNL)
• Before patient registration/randomization, written informed consent must be obtained according to ICH/EU GCP, and national/local regulations

Exclusion Criteria:

• Chemotherapy contraindicated
• Inflammatory breast cancer, tumour infiltrated axillary lymph nodes including the sentinel node.
• Other concomitant pathology compromising survival (at entry), or preventing the administration of chemotherapy with either FEC or Docetaxel
• Other serious illness or medical condition that may interfere with the understanding and giving of informed consent and the conduct of the study
• Estimated life-expectancy <10 years (irrespective of breast cancer diagnosis)
• Patient not accessible for treatment and follow up
• Endocrine treatment not according to the latest standard recommendations of the AGO Kommission "Mamma"
• Pregnancy, lactation (sufficient non-hormonal contraception in fertile women required)
• Surgery more than six weeks ago at the start of chemotherapy
• Pre-existing polyneuropathy
• Previous or concomitant other malignancy (including contralateral breast cancer) except adequately treated basal or squamous cell carcinoma of the skin or in situ carcinoma of the cervix
• Prior chemotherapy or radiotherapy or endocrine therapy