AI Article Synopsis

  • The overexpression of HER2 in breast cancer highlights the importance of molecular targeted therapy, with traditional treatments being effective only in HER2 high-expressing tumors.
  • Recent clinical trials show that the antibody-drug conjugate trastuzumab-deruxtecan can also treat tumors with low HER2 expression, prompting a need to reevaluate diagnostic criteria.
  • This shift necessitates rapid updates in diagnostic practices and raises new challenges for standardization in the assessment of tumors with low HER2 expression levels.

Article Abstract

The overexpression of HER2 in breast cancer is a classic example for molecular targeted therapy, and it has been shown that classical anti-HER2 therapeutics were only effective in patients with HER2 overexpressing tumors. Therefore, in recent decades, pathologists have been focused on the reliable identification of HER2 overexpressing tumors. Based on the results of recent clinical trials in metastatic breast cancer with antibody-drug conjugates (ADCs), this diagnostic strategy for evaluation of HER2 is currently changing. It has been shown that the ADC trastuzumab-deruxtecan is effective not only against tumors with classical HER2 overexpression, but also against HER2-low tumors. These clinical trial results lead to a paradigm shift in the treatment of patients whose tumours were previously classified as HER2 negative. In addition to the identification of HER2 (score 3+) overexpressing tumors, it is necessary to identify HER2-low expressing tumors (defined as an immunohistochemistry (IHC) score of 1+ or IHC2+ with negative in situ hybridization).Due to the therapeutic consequences, it is important to quickly adapt the diagnostic workup and reporting to the new requirements. In addition, the new therapeutic options for anti-HER2 therapy lead to new challenges for standardization as well as to new scientific questions for the characterization of tumors with low HER2 expression.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10713687PMC
http://dx.doi.org/10.1007/s00292-022-01139-4DOI Listing

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