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Clinical Implications and Treatment Strategies for ESR1 Fusions in Hormone Receptor-Positive Metastatic Breast Cancer: A Case Series.

Jamie O BrettLauren L RitterhouseErik T NewmanKelly E IrwinMegan DawsonLianne Y RyanLaura M SpringMiguel N RiveraJochen K LennerzDora Dias-SantagataLeif W EllisenAditya BardiaSeth A Wander
Published in: The oncologist (2023)
In hormone receptor-positive metastatic breast cancer (HR+ MBC), endocrine resistance is commonly due to genetic alterations of ESR1, the gene encoding estrogen receptor alpha (ERα). While ESR1 point mutations (ESR1-MUT) cause acquired resistance to aromatase inhibition (AI) through constitutive activation, far less is known about the molecular functions and clinical consequences of ESR1 fusions (ESR1-FUS). This case series discusses 4 patients with HR+ MBC with ESR1-FUS in the context of the existing ESR1-FUS literature. We consider therapeutic strategies and raise the hypothesis that CDK4/6 inhibition (CDK4/6i) may be effective against ESR1-FUS with functional ligand-binding domain swaps. These cases highlight the importance of screening for ESR1-FUS in patients with HR+ MBC while continuing investigation of precision treatments for these genomic rearrangements.
Keyphrases
  • estrogen receptor
  • metastatic breast cancer
  • systematic review
  • cell cycle
  • copy number
  • gene expression
  • machine learning
  • artificial intelligence
  • dna methylation
  • breast cancer cells