Public source
Reviewed 21 Jul 2026
Completeness Good (44%)
The Human Epidermal Growth Factor Receptor 2 (HER2) is a central biomarker in invasive breast cancer, and the HER2 status is predictive of the patient’s response to HER2-targeted treatment. According to the guidelines of the American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP), the HER2 status must be determined by protein expression and/or genetic analysis of breast tissue sections using immunohistochemistry (IHC) and/or in situ hybridization (ISH), respectively. The present protocol is a fully automatic single-cell approach for HER2 IHC quantification that follows ASCO/CAP guidelines, designed with this new scoring regime in mind, i.e. HER2-low and HER2-ultra. It is also configurable to national modifications.
No papers to support — we monitor for new evidence.
Key features
ASCO/CAP HER2 IHC guidelines
HER2 Cell-based Scoring
General Information
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Regulatory Information
Pathway:
In Vitro Diagnostic Directive (IVDD)
Class:
General IVD Devices
Not verified by Health AI Register
Scanner Brands Certified for Use (CE-IVD)
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Scanner Models Certified for Use (CE-IVD)
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Evidence & Research
No research papers or evidence on file yet.
The registry monitors publications for new evidence.
Technical Specifications
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On market since
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Pricing Information
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Source: Public | First published: Jul 30, 2025 | Last updated: Jul 21, 2026