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European Commission Approves Elacestrant for Pretreated, ESR1+, ER+/HER2– Breast Cancer

The European Commission has approved elacestrant for the treatment of postmenopausal women and men with estrogen receptor–positive, HER2-negative, locally advanced, or metastatic breast cancer with an activating ESR1 mutation who have disease progression following at least 1 line of endocrine therapy including a CDK4/6 inhibitor.

Misconceptions Remain on Gene Signature Use in Breast Cancer

Veracyte Announces New Consensus Data from PROCURE Study Presented at ESMO Breast Cancer 2022

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