This is a Phase II non-randomized, open, uncontrolled and bi-centric study of hormonal induction by exemestane (Aromasin) + tamoxifen to evaluate the effectiveness of exemestane (Aromasin) with tamoxifen on the rate of clinical response menopausal in patients with tumors of locally advanced breast. Hormone therapy will be administered at a dose of 25mg/day for exemestane and 20 mg / day for 4 months for tamoxifen.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
25mg a day during 4 months
One 20 mg tablet a day started 1 week after the first Aromasine intake
CHU de Toulouse Rangueil
Toulouse, France
Institut Claudius Regaud
Toulouse, France
Evaluate the objective response rate (complete response and partial response)
Time frame: June 2006
Pharmacokinetic interaction between Exemestane and Tamoxifen
Time frame: june 2006
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