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Bull Cancer ; 104(7-8): 608-617, 2017.
Article in French | MEDLINE | ID: mdl-28595742

ABSTRACT

INTRODUCTION: The implementation of an internal quality control is mandatory to guarantee the accuracy of HER2 status in invasive breast cancers. OBJECTIVES: To evaluate the impact of our quality control assurance on HER2 status results in invasive breast carcinomas from 2008 to 2014. METHODS: HER2 status was determined by immunohistochemistry as the first-line indication, completed by fluorescence in situ hybridization (FISH) for scores 2+ by immunohistochemistry. Internal quality control of HER2 status relied on the standardization of pre-analytical phases, the use of external controls with a known number of HER2 gene copies determined by FISH and continued monitoring of concordance between immunohistochemistry and FISH. RESULTS: The proportion of HER2-positive cases corresponding to scores 3+ by immunohistochemistry and 2+ amplified by FISH varied from 10.6% to 13.8% (median of 11.3%). The proportion of scores 2+ amplified by FISH varied from 13.3% to 32.7% during period of study. The rate of concordance between FISH and immunohistochemistry for score 0/1+ and 3+ cases were≥97%. Eight among 12 discordant cases were false positive resulting from errors in interpretation of immunohistochemistry (score 2+ instead of 3+). DISCUSSION: Calibration of immunohistochemistry on FISH for HER2 status contributes to limit variability of immunohistochemistry results due to technical issues or interpretation. The implementation of an external control of score 3+ on each slide enables accurate interpretation of score 2+ and 3+ by immunohistochemistry.


Subject(s)
Algorithms , Breast Neoplasms/genetics , Carcinoma, Ductal, Breast/genetics , Gene Amplification , Genes, erbB-2 , Quality Control , Receptor, ErbB-2/analysis , Breast Neoplasms/chemistry , Carcinoma, Ductal, Breast/chemistry , Decision Support Systems, Clinical , Female , Humans , Immunohistochemistry/methods , Immunohistochemistry/standards , Immunohistochemistry/statistics & numerical data , In Situ Hybridization, Fluorescence/methods , In Situ Hybridization, Fluorescence/standards , In Situ Hybridization, Fluorescence/statistics & numerical data , Receptor, ErbB-2/metabolism
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