Medical experts come together to share their views in this on-demand webinar replay of an interactive online discussion:
New Oral Endocrine Therapy Options for Patients with Advanced or Metastatic ER+ Breast Cancer
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The independent expert panel discussed oral SERDs efficacy and safety profiles in patients with ER+/HER2- advanced or metastatic breast cancer and their place in the treatment landscape
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They also covered how to optimise treatment selection and sequencing in ER+/HER2- advanced or metastatic breast cancer and why, when and how to test for ESR1 mutation
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The event concluded with speakers and participants engaging in a Q&A to address pressing questions
Watch the replay, broken down into 4 digestible videos, download the accompanying slides, and take the accredited e-learning using the blue button below the videos.
Clinical Takeaways
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Elacestrant is the 1st oral SERD to be FDA approved (January 2023) for postmenopausal women or adult men with ER+/HER2-, ESR1-mutated advanced or metastatic breast cancer
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FDA approved Guardant360 CDx assay as a companion diagnostic device to identify patients with ER+/HER2- advanced or metastatic breast cancer for treatment with elacestrant
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With the aim of redefining treatment landscapes for ER+/HER2- advanced and metastatic breast cancer, several oral SERDs are in clinical development both as monotherapy and in combination therapy with other targeted therapies, including CDK4/6i
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ESR1, PI3K, CDK4/6, BRCA, and AKT pathways alterations can be used as targets to guide treatment selection and sequencing decisions in ER+/HER2- advanced or metastatic breast cancer
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ESR1 mutational status can be determined without repeated tissue biopsy of a metastatic site; instead, it can be done reliably by liquid biopsy at recurrence or progression on ET