[Internal quality control on HER2 status determination in breast cancers: Experience of a cancer center]

Bull Cancer. 2017 Jul-Aug;104(7-8):608-617. doi: 10.1016/j.bulcan.2017.05.002. Epub 2017 Jun 7.
[Article in French]

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.

Keywords: Breast cancers; Cancers du sein; Contrôle qualité; Fluorescence in situ hybridization; HER2; Hybridation in situ en fluorescence; Immunohistochemistry; Immunohistochimie; Quality control.

Publication types

  • Comparative Study

MeSH terms

  • Algorithms*
  • Breast Neoplasms / chemistry
  • Breast Neoplasms / genetics*
  • Carcinoma, Ductal, Breast / chemistry
  • Carcinoma, Ductal, Breast / genetics*
  • Decision Support Systems, Clinical
  • Female
  • Gene Amplification*
  • Genes, erbB-2*
  • 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
  • Quality Control*
  • Receptor, ErbB-2 / analysis*
  • Receptor, ErbB-2 / metabolism

Substances

  • Receptor, ErbB-2