This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

EMERALD trial - elacestrant in hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

Endocrine therapy represents the cornerstone of treatment in hormone receptor-positive (HR+), HER2-negative metastatic breast cancer (mBC)

  • the natural course of this disease is marked by endocrine resistance, mainly due to Estrogen Receptor 1 (ESR1) acquired mutation (1)

The EMERALD trial, was an international, open-label, randomized phase III trial that evaluated the efficacy and safety of the oral selective estrogen receptor degrader, elacestrant, versus endocrine monotherapy (standard-of-care [SOC]) in patients with previously treated estrogen receptor (ER)-positive, HER2-negative advanced breast cancer, including patients with ESR1-mutated tumors

  • elacestrant is a novel, oral selective ER degrader
  • demonstrated a significant progression-free survival (PFS) improvement versus SOC both in the overall population and in patients with ESR1 mutations with manageable safety in a phase III trial for patients with ER-positive/HER2-negative advanced breast cancer
  • is suggested that this evidence provides a strong signal for role of testing in activating gain-of-function mutations in the estrogen receptor gene ligand-binding domain (ESR1 mutation) to guide therapy for hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer (MBC)

Reference:

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.