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Impact of CCNE1 Amplification on Molecular Signatures and Patient Outcomes in High Grade Serous Ovarian and Endometrial Cancer

Conculsion

  • CCNE1 amplification rates in HGSOC and EMCA depend on calling method
  • CCNE1 CN may increase with emergence of treatment resistance suggesting re-biopsy at time of progression may be warranted to guide therapy options
  • There are increased rates of CCNE1 amplification in Black/African American compared to white women for all tumor types but statistically significant in serous EMCA and endometrioid EMCA
  • PIK3CA, ARID1A, PTEN, KRAS, NF1, and RB1 mutations were inversely associated with CCNE1 amplification
  • CCNE1 is significantly likely to co-occur with ERBB2 amplification, especially in endometrioid EMCA
  • CCNE1 amplified tumors appear overall non-immunogenic
  • While there is some overlap with FOLR1+ and HER2+ other targeted agents will be needed to exploit CCNE1 amplification
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