Ontology highlight
ABSTRACT: Background
Conventional HER2-targeting therapies improve outcomes for patients with HER2-positive breast cancer (BC), defined as tumors showing HER2 protein overexpression by immunohistochemistry and/or ERBB2 gene amplification determined by in situ hybridization (ISH). Emerging HER2-targeting compounds show benefit in some patients with neither HER2 protein overexpression nor ERBB2 gene amplification, creating a need for new assays to select HER2-low tumors for treatment with these compounds. We evaluated the analytical performance of a targeted mass spectrometry-based assay for quantifying HER2 protein in formalin-fixed paraffin-embedded (FFPE) and frozen BC biopsies.Methods
We used immunoaffinity-enrichment coupled to multiple reaction monitoring-mass spectrometry (immun
SUBMITTER: Kennedy JJ
PROVIDER: S-EPMC8260184 | biostudies-literature | 2021 Jul
REPOSITORIES: biostudies-literature