AI Article Synopsis

  • The study investigated how hormone receptors and HER-2/neu status change between a primary breast cancer and its metastatic lesions.
  • The research found significant discordance rates, with 27.7% for ER, 40.7% for PR, and 19.6% for HER-2/neu when comparing primary tumors to their metastases.
  • Patients with all three hormone receptors negative faced worse survival outcomes, highlighting the importance of evaluating metastatic lesions for potential targeted therapies.

Article Abstract

Background: Hormone receptor and HER-2/neu discordance between the primary lesion and first metastasis has been reported. This study was performed to determine further biomarker discordance rates between the first and subsequent metastatic breast cancer lesions.

Methods: We performed a retrospective review of paired biomarkers from primary breast cancers compared to first reported and subsequent metastases from 103 patients with breast cancer. The estrogen receptor (ER), progesterone receptor (PR), and HER-2/neu status were reported at all three time points. In addition, hormone, cytotoxic, and targeted treatments were recorded for primary and metastatic disease, and survival was determined.

Results: Between the primary and first metastases, discordance rates for ER, PR, and HER-2/neu were 15.8%, 33.7%, and 14.3%, respectively. There was discordance between the first and second metastases for the ER receptor in 18.8%, PR receptor in 19.8%, and HER-2/neu in 10.7%. Overall, there was discordance between the primary tumor and either the first or second metastases for ER in 27.7%, PR receptor in 40.7%, and HER-2/neu in 19.6% of cases. Discordance of either ER or PR affected survival, with worse survival experienced by those patients with all three hormone receptors remaining negative, and intermediate survival reported for those with discordant tumors (ER χ=14.27, =0.0008; PR χ=11.31, =0.0035). There was no difference in survival for patients whose HER-2/neu tumors were discordant.

Conclusion: This study demonstrated that continued metastatic disease evolution may be associated with different tumor biology and that studies of metastatic lesions appear warranted, especially if targeted therapy is an option.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546587PMC
http://dx.doi.org/10.2147/BCTT.S137709DOI Listing

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