Elacestrant (oral selective estrogen receptor degrader) Versus Standard Endocrine Therapy for Estrogen Receptor–Positive, Human Epidermal Growth Factor Receptor 2–Negative Advanced Breast Cancer: Results From the Randomized Phase III EMERALD Trial
Université de Versailles Saint-Quentin-en-Yvelines · Université Paris-Saclay · +36 more institutions
Abstract
PURPOSE Patients with pretreated estrogen receptor (ER)–positive/human epidermal growth factor receptor 2 (HER2)–negative advanced breast cancer have poor prognosis. Elacestrant is a novel, oral selective ER degrader that demonstrated activity in early studies. METHODS This randomized, open-label, phase III trial enrolled patients with ER-positive/HER2-negative advanced breast cancer who had one-two lines of endocrine therapy, required pretreatment with a cyclin-dependent kinase 4/6 inhibitor, and ≤ 1 chemotherapy. Patients were randomly assigned to elacestrant 400 mg orally once daily or standard-of-care (SOC) endocrine monotherapy. Primary end points were progression-free survival (PFS) by blinded…
Citation impact
- FWCI
- 90.05
- Percentile
- 100%
- References
- 36
Authors
29- FBFrançois‐Clément BidardCorresponding
Université de Versailles Saint-Quentin-en-Yvelines, Université Paris-Saclay, Institut Curie
- VKVirginia Kaklamani
The University of Texas at San Antonio Health Science Center
- PNPatrick Neven
Universitair Ziekenhuis Leuven
- GSGuillermo Streich
- AJAlberto J. Montero
University Hospitals Seidman Cancer Center, Case Western Reserve University
Topics & keywords
- Medicine
- Internal medicine
- Hazard ratio
- Estrogen receptor
- Breast cancer
- Oncology
- Adverse effect
- Fulvestrant
- Good health and well-being