An observational study in patients with advanced ER+, HER2 negative breast cancer, who are treated with everolimus and exemestane in combination. The objective of the study is to assess the safety pattern of everolimus in a real world setting.
Study Type
OBSERVATIONAL
Enrollment
7
Aalborg Universitetshospital, Clinical Research unit Department of oncology, Klinik Kirurgi-kræft, Hobrovej 18-22
Aalborg, Denmark
Onkologisk Afdelning, SVS Esbjerg
Esbjerg, Denmark
Department of Oncology, Odense University Hospital
Odense, Denmark
Adverse Events
Time frame: Up to 2.5 years
Progression free survival
Time frame: Up to 2.5 years
Overall response rate
Time frame: Up to 2.5 years
Clinical benefit rate
Time frame: Up to 2.5 years
Overall survival
Time frame: Up to 2.5 years
Time on treatment with everolimus
Time frame: Up to 2.5 years
Reason for stopping treatment with everolimus
Time frame: Up to 2.5 years
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