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Updated: Oct 10, 2025

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Abstract:
In the phase III EMERALD trial, the investigational oral selective estrogen receptor degrader elacestrant offered a modest but statistically significant improvement in progression-free survival in patients with ER-positive/HER2-negative breast cancer previously treated with endocrine therapy and a CDK4/6 inhibitor.
Insights
Elacestrant, an oral selective estrogen receptor degrader, showed a modest but significant improvement in progression-free survival for patients with advanced ER-positive/HER2-negative breast cancer. This finding is relevant for patients previously treated with endocrine therapy and CDK4/6 inhibitors.
Area of Science:
- Oncology
- Endocrinology
- Pharmacology
Background:
- The EMERALD trial investigated elacestrant, an oral selective estrogen receptor degrader (SERD), in patients with advanced ER-positive/HER2-negative breast cancer.
- Patients had prior treatment with endocrine therapy and a CDK4/6 inhibitor, a common scenario in advanced disease.
Discussion:
- Elacestrant demonstrated a statistically significant improvement in progression-free survival (PFS) compared to standard care in this heavily pretreated population.
- The modest magnitude of PFS benefit warrants further investigation into predictive biomarkers and optimal sequencing.
Key Insights:
- Elacestrant offers a new oral treatment option for patients with ER+/HER2- advanced breast cancer progressing after CDK4/6 inhibitors and endocrine therapy.
- The study provides valuable data on the efficacy of oral SERDs in a challenging clinical setting.
Outlook:
- Further research may explore elacestrant in combination therapies or earlier lines of treatment.
- Identifying patient subgroups who derive maximal benefit from elacestrant will be crucial for personalized treatment strategies.
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