Molecular Oncology Almanac
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    1. Propositions
    2. prop:vtxr:132

    Therapeutic Response

    HER2-negative and PR positive status confers therapeutic sensitivity to Everolimus in combination with Exemestane in patients with Invasive Breast Carcinoma.

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    Statements

    Source and description
    Afinitor (everolimus) [package insert]. FDA.

    The U.S. Food and Drug Administration granted approval to everolimus in combination with exemestane for the treatment of patients who are postmenopausal women with advanced hormone receptor-positive, HER2 negative breast cancer after failure of treatment with letrozole or anastrozole.
    Afinitor (everolimus) [product information]. EMA.

    The European Medicines Agency (EMA) has authorized everolimus in combination with exemestane for the treatment of adult patients with hormone receptor-positive, HER2/neu negative advanced breast cancer in postmenopausal women without symptomatic visceral disease after recurrence or progression following a non-steroidal aromatase inhibitor.

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