Alternate Title
Basic Trial Information
Objectives
Entry Criteria
Expected Enrollment
Outcomes
Outline
Trial Contact Information
Registry Information

Alternate Title

Genetic Testing or Clinical Assessment in Determining the Need for Chemotherapy in Women With Node-Negative Breast Cancer

Basic Trial Information

Phase Type Status Age Sponsor Protocol IDs Phase III Treatment Active 18 to 70 Other, Pharmaceutical / Industry EORTC-10041 EUDRACT-2005-002625-31, BIG-3-04, NOVARTIS-EORTC-10041, ROCHE-EORTC-10041, SANOFI-AVENTIS-EORTC-10041, NCT00433589

Objectives

Primary

1. Compare a molecular profiling approach (70-gene signature) vs usual clinical assessment in assigning adequate risk categories (and the need to receive adjuvant chemotherapy or not) to breast cancer patients with 0-3 positive lymph nodes.
2. Compare the efficacy and long-term toxicities of docetaxel and capecitabine vs standard anthracycline-based chemotherapy regimens in these patients.
3. Determine the best endocrine treatment strategy (i.e., letrozole for 7 years vs sequential tamoxifen for 2 years followed by letrozole for 5 years) in these patients.

Secondary

1. Compare both relative (hazard ratio) and absolute (percentage at 5 years) efficacy of these regimens, in terms of disease-free survival (DFS), distant metastasis-free survival (DMFS) and overall survival (OS), in these patients.
2. Determine overall estimates of efficacy (DFS, DMFS, OS) for each treatment strategy according to clinical-pathological prognosis and molecular prognosis in these patients.
3. Estimate the percentage of patients receiving chemotherapy per each prognostic method.
4. Identify predictive gene expression profiles of clinical response/resistance to anthracycline-based and docetaxel-capecitabine chemotherapy in these patients.
5. Compare novel gene expression signatures predicting clinical response in patients treated with sequential tamoxifen-letrozole vs letrozole alone.
6. Compare the OS distributions in patients treated with these regimens.
7. Compare the early and late toxicities of these regimens in these patients.
8. Evaluate adjuvant endocrine treatment success or failure in the subgroup of postmenopausal patients with endocrine-responsive disease.
9. Compare the safety profile of these two endocrine therapy regimens in these patients.

Entry Criteria

Disease Characteristics:

• Histologically confirmed invasive breast cancer meeting the following criteria:
  • T1, T2, or operable T3 disease
  • Zero to three positive lymph nodes and no distant metastases
  • Unilateral tumor
    • Multifocal tumors are allowed provided that they have identical histology
    • Ductal carcinoma in situ or lobular carcinoma in situ allowed if invasive cancer is present



• Operable disease
  • Must have undergone breast-conserving surgery or mastectomy with either a sentinel node procedure or full axillary clearance
    • Radiotherapy is mandatory in the case of breast-conserving surgery
    • Unresectable positive deep margins and adjuvant radiotherapy with all other margins negative allowed



• Patients eligible for inclusion in the chemotherapy randomization must meet one of the following criteria:
  • High-risk of recurrence according to both the clinical-pathological criteria and the 70-gene signature
  • High risk of recurrence according to the clinical-pathological criteria and low-risk of recurrence according to the 70-gene signature and are randomized to use the clinical-pathological criteria for chemotherapy decision
  • Low-risk of recurrence according to the clinical-pathological criteria and high-risk of recurrence according to the 70-gene signature and are randomized to use the 70-gene signature for chemotherapy decision



• Patients eligible for inclusion in the endocrine therapy randomization must meet all of the following criteria:
  • Endocrine-responsive disease
  • Hormone receptor-positive disease (estrogen receptor-positive, progesterone receptor-positive, or both)

Prior/Concurrent Therapy:

• See Disease Characteristics
• No prior chemotherapy, hormonal therapy, or radiotherapy
• No participation in another investigational drug study within the past 4 weeks
• No systemic hormone replacement therapy (with or without progestins) for more than 3 months in duration
• Patients eligible for inclusion in the chemotherapy randomization must meet all of the following additional criteria:
  • Interval between definitive surgery and start of chemotherapy 6-8 weeks
  • No prior organ allografts requiring immunosuppressive therapy
  • No concurrent sorivudine or chemically related analogues, such as brivudine
• Patients eligible for inclusion in the endocrine therapy randomization must meet all of the following additional criteria:
  • No prior high-dose systemic corticosteroids (except as antiemetic treatment), immunotherapy, or biological response modifiers (e.g., interferon)
  • No prior adjuvant antiestrogen therapy for > 1 month immediately after surgery, radiotherapy, and/or chemotherapy
  • No hormone replacement therapy within the past 4 weeks
  • No antiestrogens as chemoprevention for breast cancer within the past 18 months
• No concurrent primary prophylaxis with filgrastim (G-CSF), sargramostim (GM-CSF), or pegfilgrastim
• No other concurrent treatment during endocrine therapy, including the following:
  • Anticancer therapy (anti-estrogens, aromatase inhibitors, chemotherapy)
  • Investigational agents
  • Raloxifene or other selective estrogen-receptor modulators
  • Hormonal contraceptives (including depot injections and implants)
    • Intrauterine devices, including progesterone-coated, allowed
  • Oral or transdermal hormonal treatments, including estrogen, progesterone, androgen, or aromatase inhibitor
    • Local vaginal (topical) estrogens with minimal systemic absorption allowed for severe vaginal dryness/dyspareunia
• Concurrent bisphosphonates allowed

Patient Characteristics:

• Female
• WHO performance status 0-1
• Neutrophil count > 1,500/mm³
• Platelet count > 100,000/mm³
• Creatinine clearance at least 50 mL/min OR creatinine up to 1.5 times upper limit of normal (ULN)
• ALT and AST up to 2.5 times ULN
• Alkaline phosphatase up to 2.5 times ULN
• Bilirubin up to 2.0 times ULN
• Normal echocardiogram (ECHO) compatible with chemotherapy treatment
• No serious cardiac illness or medical condition including, but not limited to, any of the following:
  • History of documented congestive heart failure
  • High-risk uncontrolled arrhythmias
  • Angina pectoris requiring antianginal medication
  • Clinically significant valvular heart disease
  • Evidence of transmural infarction on ECG
  • Poorly controlled hypertension (e.g., systolic blood pressure [BP] > 180 mm Hg or diastolic BP > 100 mm Hg)
  • Symptomatic coronary artery disease or a myocardial infarction within the past 12 months
  • Other risk factors that contraindicate the use of anthracycline-based chemotherapy
• No serious uncontrolled infection or other serious uncontrolled disease
• No other invasive cancer within the past 5 years except for adequately treated carcinoma in situ of the cervix or nonmelanoma skin cancer
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective barrier contraception
• No psychological, familial, sociological, or geographical condition that would preclude study treatment
• No psychiatric disability
• No history of uncontrolled seizures or CNS disorders
• Patients eligible for inclusion in the chemotherapy randomization must meet all of the following additional criteria:
  • LVEF normal by ECHO or MUGA
  • No prior severe hypersensitivity reaction to drugs formulated with polysorbate 80
  • Must have physical integrity of the upper gastrointestinal tract
  • Able to swallow tablets
  • No malabsorption syndrome
• No prior thromboembolic disorder, deep vein thrombosis, or pulmonary emboli (for patients eligible for inclusion in the endocrine therapy randomization)

Expected Enrollment

A total of 6,000 patients will be accrued for this study.

Outcomes

Distant metastasis-free survival at 5 years
Disease-free survival (DFS)

Proportion of patients treated with chemotherapy based on clinical prognosis compared to 70-gene signature prognosis
Overall survival at 5 years
DFS at 5 years
Safety (early and late)

Outline

This is a partially randomized, open-label, prospective, multicenter study.

Patients with both clinical high-risk (CHR) and genomic high-risk (GHR) disease are assigned to receive chemotherapy. Patients with both clinical low-risk (CLR) and genomic low-risk (GLR) disease do not receive chemotherapy. Patients with discordant risk between the 2 decision-making tools (standard clinical-pathological criteria vs 70-gene signature criteria) are randomized to receive chemotherapy or not.

• Chemotherapy: Patients are stratified according to participating center, risk group (GHR/CLR vs GLR/CHR), hormone receptor status (estrogen receptor [ER] positive and/or progesterone receptor [PR] positive vs ER and PR negative), age (< 50 years vs at least 50 years), HER2/neu status (positive vs negative vs unknown), method of axillary evaluation (sentinel only vs dissection), and type of surgery (mastectomy vs quadrantectomy/tumorectomy). Patients are randomized to 1 of 2 treatment arms.
  • Arm I (anthracycline-based): Patients may receive 1 of the following regimens*:
    • FEC 100: Patients receive fluorouracil IV, epirubicin hydrochloride IV, and cyclophosphamide IV on day 1. Treatment repeats every 3 weeks for 6 courses.
    
    
    
    • Canadian CEF: Patients receive oral cyclophosphamide on days 1-14 (or IV on days 1 and 8) and epirubicin hydrochloride IV and fluorouracil IV on days 1 and 8. Treatment repeats every 4 weeks for 6 courses.
    
    
    
    • CAF:Patients receive cyclophosphamide IV, doxorubicin hydrochloride IV, and fluorouracil IV on day 1. Treatment repeats every 4 weeks for 6 courses.
    
    
    
    • FAC: Patients receive cyclophosphamide IV and doxorubicin hydrochloride IV on day 1 and fluorouracil IV on days 1 and 8. Treatment repeats every 3 weeks for 6 courses.
    
    
    
    • E-CMF: 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 and 8. Treatment repeats every 4 weeks for 4 courses.
    
    
    

     [Note: *Patients who refuse randomization may be treated with another chemotherapy regimen and still be included in the study.]

  
  
  
  • Arm II (docetaxel and capecitabine): Patients receive docetaxel IV over 1 hour on day 1 and oral capecitabine twice daily on days 1-14. Treatment repeats every 3 weeks for 6 courses.
  
  
  



• Endocrine therapy (all postmenopausal and some premenopausal* patients who have endocrine-responsive tumors**): Patients are stratified according to participating center, risk group (GHR/CHR vs GHR/CLR vs GLR/CHR vs GLR/CLR), adjuvant chemotherapy (no vs nonrandomized vs arm I vs arm II), endocrine sensitivity (both ER and PR positive vs either ER or PR positive), age (< 50 years vs at least 50 years), HER2/neu status (positive vs negative vs unknown), method of axillary evaluation (sentinel only vs dissection), and type of surgery (mastectomy vs quadrantectomy/tumorectomy).

  Therapy begins after prior surgery in patients who did not receive chemotherapy and after chemotherapy in those who did. Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive oral tamoxifen citrate once daily for 2 years. Patients then receive oral letrozole once daily for 5 years.
  
  
  
  • Arm II: Patients receive oral letrozole once daily for 7 years.

     [Note: *Premenopausal women (< 50 years) must undergo adequate ovarian suppression (gonadotropin releasing hormone, bilateral oophorectomy, or bilateral ovarian radiation).]

     [Note: **Patients who have endocrine-responsive tumors but refuse randomization should receive standard endocrine therapy and may remain on study.]

  
  
  

After completion of study treatment, patients are followed annually for at least 15 years.

Trial Contact Information

Trial Lead Organizations

European Organization for Research and Treatment of Cancer

Emiel Rutgers, MD, PhD, FRCS, Study coordinator		Ph: 32-2-774-16-41 Email: e.rutgers@nki.nl
Martine Piccart-Gebhart, MD, PhD, Study coordinator		Ph: 32-2-541-3206 Email: martine.piccart@bordet.be
Fatima Cardoso, MD, Study coordinator		Ph: 32-2-541-3082 Email: fatima.cardoso@bordet.be

Netherlands
	Amsterdam
	Netherlands Cancer Institute - Antoni van Leeuwenhoek Hospital
		Emiel Rutgers, MD, PhD, FRCS	Ph:  31-20-512-2551

Registry Information
Official Title		MINDACT (Microarray In Node-negative Disease may Avoid Chemotherapy): A Prospective, Randomized Study Comparing the 70-Gene Signature With the Common Clinical-Pathological Criteria in Selecting Patients for Adjuvant Chemotherapy in Node-Negative Breast Cancer
Trial Start Date		2006-12-07
Trial Completion Date		2019-03-30 (estimated)
Registered in ClinicalTrials.gov		NCT00433589
Date Submitted to PDQ		2006-12-11
Information Last Verified		2008-06-18