The purpose of this study was to give access to postmenopausal women with estrogen sensitive primary breast cancer to exemestane for the adjuvant treatment of breast cancer after the use of tamoxifen and to collect all serious adverse events.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
1,549
Exemestane 25 mg oral tablet once daily for a maximum of 3 years
Assess for serious adverse events
Time frame: Months 3, 6, 12, 18, 24, and 30; Follow-up visit 28 days posttreatment
Safety Surveillance Program
Time frame: Duration of trial
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Aalst, Belgium
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Antwerp, Belgium
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Arlon, Belgium
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Bonheiden, Belgium
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Bouge, Belgium
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Bruges, Belgium
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