Abstract

The EMERALD clinical trial showed significantly prolonged progression-free survival (PFS) and a manageable toxicity profile for elacestrant vs SOC endocrine therapy in patients (pts) with ER+/HER2- mBC following progression on prior endocrine and CDK4/6 inhibitor therapy. Benefit was observed in the overall population and in pts with ESR1 mutations (mESR1). Here, we report a subgroup analysis from EMERALD comparing efficacy with elacestrant to fulvestrant or AI.

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