Molecular Oncology Almanac
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    2. prop:vtxr:140

    Therapeutic Response

    ER positive and HER2-negative status confers therapeutic sensitivity to Fulvestrant in combination with Ribociclib in patients with Invasive Breast Carcinoma.

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    Statements

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    Faslodex (fulvestrant) [package insert]. FDA.

    The U.S. Food and Drug Administration granted approval to fulvestrant in combination with ribociclib for the treatment of patients who are postmenopausal women with hormone receptor (HR)-positive, HER2-negative advanced or metastatic breast cancer, as initial endocrine based therapy or following disease progression on endocrine therapy.
    Kisqali (ribociclib) [package insert]. FDA.

    The U.S. Food and Drug Administration granted approval to ribociclib in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer as either an initial endocrine-based therapy or following disease progression on endocrine therapy.
    Kisqali (ribociclib) [product monograph]. HC.

    Health Canada approved ribociclib, in combination with fulvestrant, for the treatment ostmenopausal women, with HR-positive, HER2-negative advanced or metastatic breast cancer, as initial endocrine-based therapy or following disease progression on endocrine therapy.

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