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

Martin-Luther-Universität Halle-Wittenberg

Status and phase: Unknown; Phase 3

Conditions: Breast Cancer

Treatments: Drug: 5-Fluorouracil, Epirubicin, Cyclophosphamide, Docetaxel

Study type: Interventional

Funder types: Other

Identifiers

NCT01222052

GBG 42

Details and patient eligibility

About

In low-risk node-negative breast cancer patients adjuvant chemotherapy should be spared. The identification of this subgroup can be based either on clinical and pathological or on tumour-biological criteria. Due to their high prognostic impact, the tumour-biological invasion markers uPA/PAI-1 (urokinase-type plasminogen activator and its inhibitor PAI-1) are potential candidates to effectively assess the risk of relapse in node-negative breast cancer. This study is aimed to compare the risk assessment by the traditional clinico-pathological factors and by tumour-biological factors. The second study question refers to the comparison between an adjuvant combination treatment with FE100C*6 and a sequential treatment with FE100C*3 and Docetaxel*3.

Full description

1. To compare FEC*6 with FEC*3 followed by DOC*3 with regard to:

   • the primary endpoint of the study: Disease-Free Survival (DFS)
   • the secondary endpoints: Overall Survival (OS), compliance, and toxicity of chemotherapy in each patient group

2. To compare patients with low risk according to clinico-pathological versus those according to biological risk criteria with regard to:

   • the proportion of low risk versus high risk patients
   • DFS
   • OS (secondary endpoint)

Enrollment: 4,150 patients

Sex: Female

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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4,150 participants in 3 patient groups

Arm A Taxane-containing

Experimental group

Description:

3 courses FEC q3weeks followed by 3 courses Docetaxel q3weeks

Treatment:

Drug: 5-Fluorouracil, Epirubicin, Cyclophosphamide, Docetaxel

Arm B standard anthracyclin

Active Comparator group

Description:

6 courses of FEC q3weeks

Treatment:

Drug: 5-Fluorouracil, Epirubicin, Cyclophosphamide, Docetaxel

Observation

No Intervention group