RATIONALE: Estrogen can cause the growth of breast cancer cells. Hormone therapy using anastrozole or fulvestrant may fight breast cancer by lowering the amount of estrogen the body makes or by blocking the use of estrogen by the tumor cells. Giving hormone therapy before surgery may be an effective treatment for breast cancer. It is not yet known whether anastrozole is more effective than fulvestrant when given before surgery in treating women with breast cancer. PURPOSE: This randomized phase II trial is studying anastrozole to see how well it works compared with fulvestrant in treating postmenopausal women with stage II or stage III breast cancer that can be removed by surgery.
OBJECTIVES: Primary * To compare the clinical response rates (complete and partial responses) at 6 months in postmenopausal women with operable stage II or III breast cancer treated with neoadjuvant anastrozole vs fulvestrant. Secondary * To compare the breast surgery conservation rate in patients treated with these drugs. * To correlate imaging findings by mammography, ultrasonography, and MRI with histological and clinical response in these patients and with sensitivity profile to these drugs. * To compare histological response in patients treated with these drugs. * To define criteria appropriate for neoadjuvant hormonal therapy. * To correlate baseline molecular characteristics and modifications during treatment with response in these patients. * To compare the tolerability of these drugs in these patients. * To compare the serum proteomic profile of patients treated with these drugs. * To correlate 3-year event-free and overall survival rates with clinical and histological response in these patients. OUTLINE: This is a multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive oral anastrozole once daily for 4-6 months in the absence of clinical progression. * Arm II: Patients receive fulvestrant intramuscularly on days 1, 15, and 29 in the first month and then every 28 days in each subsequent month. Treatment continues for 4-6 months in the absence of clinical progression. Patients in both arms then undergo surgery and radiotherapy according to institutional guidelines. Patients then receive adjuvant hormonal therapy for at least 5 years. After completion of study therapy, patients are followed periodically for up to 3 years.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
116
1 mg/day for either 4 months or 6 months depending on the clinical evaluation
500mg at day 1, day 15 and day 29 500mg every 28 days for either 4 months or 6 months depending on the clinical evaluation
Centre Jean Perrin
Clermont-Ferrand, France
Hopital Dupuytren
Limoges, France
Institut Curie Hopital
Paris, France
Centre Eugene Marquis
Rennes, France
Centre Rene Huguenin
Saint-Cloud, France
Institut Gustave Roussy
Villejuif, France
Clinical tumor response as assessed by RECIST criteria
Time frame: 6 months
Breast surgery conservation rate
Time frame: Post surgery
Histological tumor response as assessed by the Sataloff scale
Time frame: Post surgery
Tumor response as assessed by mammography, ultrasonography (RECIST criteria), and MRI
Time frame: at baseline, after the first month of treatment, and then before surgery
Biological prognosis and predictive response factors
Time frame: 3 years
Relapse-free survival rate
Time frame: 3 years
Event-free survival rate
Time frame: 3 years
Overall survival rate
Time frame: 3 years
Toxicity as assessed by NCI CTCAE v3.0
Time frame: During neoadjuvant treatment
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.