
Emerging Technologies for Assessing HER2 Amplification
Author(s) -
Frédérique PenaultLlorca,
Michael Bilous,
Mitch Dowsett,
Wedad Hanna,
R. Yoshiyuki Osamura,
Josef Rüschoff,
Marc J. van de Vijver
Publication year - 2009
Publication title -
american journal of clinical pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.859
H-Index - 128
eISSN - 1943-7722
pISSN - 0002-9173
DOI - 10.1309/ajcpv2i0hgpmgbsq
Subject(s) - cish , chromogenic in situ hybridization , immunohistochemistry , in situ hybridization , trastuzumab , human epidermal growth factor receptor 2 , fluorescence in situ hybridization , chromogenic , concordance , breast cancer , pathology , in situ , fish <actinopterygii> , biology , medicine , cancer , chemistry , bioinformatics , genetics , messenger rna , organic chemistry , chromatography , fishery , gene , chromosome
Patients with human epidermal growth factor receptor-2 (HER2)+ breast cancer are eligible for trastuzumab treatment; therefore, accurate assessment of HER2 status is essential. Until recently, only 2 methods were validated for determining the HER2 status of breast tumors in the routine diagnostic setting: immunohistochemical analysis and fluorescence in situ hybridization (FISH). Recently, bright-field in situ hybridization techniques such as chromogenic in situ hybridization (CISH) and silver-enhanced in situ hybridization (SISH), which combine features of immunohistochemical analysis and FISH, have been introduced for the determination of HER2 status. These new techniques use a peroxidase enzyme-labeled probe with chromogenic detection, instead of a fluorescent-labeled probe, allowing results to be visualized by standard bright-field microscopy. Thus, the histologic features and HER2 status of a specimen can be evaluated in parallel. Moreover, signals do not decay over time. This review discusses recent publications regarding CISH and SISH testing, including results scoring and concordance between FISH and immunohistochemical analysis.