Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

dc.contributor.authorWolff, Antonio C.
dc.contributor.authorHammond, M. Elizabeth Hale
dc.contributor.authorAllison, Kimberly H.
dc.contributor.authorHarvey, Brittany E.
dc.contributor.authorMangu, Pamela B.
dc.contributor.authorBartlett, John M. S.
dc.contributor.authorBilous, Michael
dc.contributor.authorEllis, Ian O.
dc.contributor.authorFitzgibbons, Patrick
dc.contributor.authorHanna, Wedad
dc.contributor.authorJenkins, Robert B.
dc.contributor.authorPress, Michael F.
dc.contributor.authorSpears, Patricia A.
dc.contributor.authorVance, Gail H.
dc.contributor.authorViale, Giuseppe
dc.contributor.authorMcShane, Lisa M.
dc.contributor.authorDowsett, Mitchell
dc.contributor.departmentMedical and Molecular Genetics, School of Medicineen_US
dc.date.accessioned2019-04-03T19:39:15Z
dc.date.available2019-04-03T19:39:15Z
dc.date.issued2018
dc.description.abstractPurpose To update key recommendations of the American Society of Clinical Oncology/College of American Pathologists human epidermal growth factor receptor 2 (HER2) testing in breast cancer guideline. Methods Based on the signals approach, an Expert Panel reviewed published literature and research survey results on the observed frequency of less common in situ hybridization (ISH) patterns to update the recommendations. Recommendations Two recommendations addressed via correspondence in 2015 are included. First, immunohistochemistry (IHC) 2+ is defined as invasive breast cancer with weak to moderate complete membrane staining observed in > 10% of tumor cells. Second, if the initial HER2 test result in a core needle biopsy specimen of a primary breast cancer is negative, a new HER2 test may (not “must”) be ordered on the excision specimen based on specific clinical criteria. The HER2 testing algorithm for breast cancer is updated to address the recommended work-up for less common clinical scenarios (approximately 5% of cases) observed when using a dual-probe ISH assay. These scenarios are described as ISH group 2 (HER2/chromosome enumeration probe 17 [CEP17] ratio ≥ 2.0; average HER2 copy number < 4.0 signals per cell), ISH group 3 (HER2/CEP17 ratio < 2.0; average HER2 copy number ≥ 6.0 signals per cell), and ISH group 4 (HER2/CEP17 ratio < 2.0; average HER2 copy number ≥ 4.0 and < 6.0 signals per cell). The diagnostic approach includes more rigorous interpretation criteria for ISH and requires concomitant IHC review for dual-probe ISH groups 2 to 4 to arrive at the most accurate HER2 status designation (positive or negative) based on combined interpretation of the ISH and IHC assays. The Expert Panel recommends that laboratories using single-probe ISH assays include concomitant IHC review as part of the interpretation of all single-probe ISH assay results.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationWolff, A. C., Hammond, M. E. H., Allison, K. H., Harvey, B. E., Mangu, P. B., Bartlett, J. M. S., … Dowsett, M. (2018). Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update. Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology, 36(20), 2105–2122. https://doi.org/10.1200/JCO.2018.77.8738en_US
dc.identifier.urihttps://hdl.handle.net/1805/18766
dc.language.isoenen_US
dc.publisherASCOen_US
dc.relation.isversionof10.1200/JCO.2018.77.8738en_US
dc.relation.journalJournal of Clinical Oncologyen_US
dc.rightsPublisher Policyen_US
dc.sourcePublisheren_US
dc.subjecthuman epidermal growth factor receptor 2en_US
dc.subjectbreast canceren_US
dc.subjecttestingen_US
dc.titleHuman Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Updateen_US
dc.typeArticleen_US
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