Pathological identification of HER2-low breast cancer: Tips, tricks, and troubleshooting for the optimal test
- PMID: 37077201
- PMCID: PMC10106673
- DOI: 10.3389/fmolb.2023.1176309
Pathological identification of HER2-low breast cancer: Tips, tricks, and troubleshooting for the optimal test
Abstract
The introduction of novel anti-HER2 antibody-drug conjugates (ADC) for the treatment of HER2-low breast cancers has transformed the traditional dichotomy of HER2 status to an expanded spectrum. However, the identification of HER2-low (i.e., immunohistochemistry (IHC) score 1 + or IHC score 2+, without gene amplification) tumors is challenged by methodological and analytical variables that might influence the sensitivity and reproducibility of HER2 testing. To open all possible therapeutic opportunities for HER2-low breast cancer patients the implementation of more accurate and reproducible testing strategies is mandatory. Here, we provide an overview of the existing barriers that may trouble HER2-low identification in breast cancer and discuss practical solutions that could enhance HER-low assessment.
Keywords: HER2; HER2-low; breast cancer; immunohistochemistry; in situ hybridization; pathology; precision medicine.
Copyright © 2023 Sajjadi, Guerini-Rocco, De Camilli, Pala, Mazzarol, Venetis, Ivanova and Fusco.
Conflict of interest statement
NF has received honoraria for consulting, advisory role, speaker bureau, travel, and/or research grants from MSD, Boehringer Ingelheim, Novartis, Roche, AstraZeneca, Daiichi Sankyo, GlaxoSmithKline (GSK), Gilead, Diaceutics, Adicet Bio, and Sermonix. EGR has received honoraria for consulting, advisory role, speaker bureau, travel, and/or research grants from Thermo Fisher Scientific, Novartis, AstraZeneca, Roche, Biocartis, Exact Science, GSK, and Illumina. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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