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Interobserver Variation in the Assessment of Immunohistochemistry Expression Levels in HER2-Negative Breast Cancer: Can We Improve the Identification of Low Levels of HER2 Expression by Adjusting the Criteria? An International Interobserver Study

  • Ximena Baez-Navarro*
  • , Mieke R. van Bockstal
  • , Diënna Nawawi
  • , Glenn Broeckx
  • , Cecile Colpaert
  • , Shusma C. Doebar
  • , Marieke C.H. Hogenes
  • , Esther Koop
  • , Kathleen Lambein
  • , Dieter J.E. Peeters
  • , Renata H.J.A. Sinke
  • , Johannes Bastiaan van Brakel
  • , José van der Starre-Gaal
  • , Bert van der Vegt
  • , Koen van de Vijver
  • , Celien P.H. Vreuls
  • , Willem Vreuls
  • , Pieter J. Westenend
  • , Carolien H.M. van Deurzen
  • *Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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Abstract

The classification of human epidermal growth factor receptor 2 (HER2) expression is optimized to detect HER2-amplified breast cancer (BC). However, novel HER2-targeting agents are also effective for BCs with low levels of HER2. This raises the question whether the current guidelines for HER2 testing are sufficiently reproducible to identify HER2-low BC. The aim of this multicenter international study was to assess the interobserver agreement of specific HER2 immunohistochemistry scores in cases with negative HER2 results (0, 1+, or 2+/in situ hybridization negative) according to the current American Society of Clinical Oncology/College of American Pathologists (ASCO/CAP) guidelines. Furthermore, we evaluated whether the agreement improved by redefining immunohistochemistry (IHC) scoring criteria or by adding fluorescent in situ hybridization (FISH). We conducted a 2-round study of 105 nonamplified BCs. During the first assessment, 16 pathologists used the latest version of the ASCO/CAP guidelines. After a consensus meeting, the same pathologists scored the same digital slides using modified IHC scoring criteria based on the 2007 ASCO/CAP guidelines, and an extra “ultralow” category was added. Overall, the interobserver agreement was limited (4.7% of cases with 100% agreement) in the first round, but this was improved by clustering IHC categories. In the second round, the highest reproducibility was observed when comparing IHC 0 with the ultralow/1+/2+ grouped cluster (74.3% of cases with 100% agreement). The FISH results were not statistically different between HER2-0 and HER2-low cases, regardless of the IHC criteria used. In conclusion, our study suggests that the modified 2007 ASCO/CAP criteria were more reproducible in distinguishing HER2-0 from HER2-low cases than the 2018 ASCO/CAP criteria. However, the reproducibility was still moderate, which was not improved by adding FISH. This could lead to a suboptimal selection of patients eligible for novel HER2-targeting agents. If the threshold between HER2 IHC 0 and 1+ is to be clinically actionable, there is a need for clearer, more reproducible IHC definitions, training, and/or development of more accurate methods to detect this subtle difference in protein expression levels.

Original languageEnglish
Article number100009
JournalModern Pathology
Volume36
Issue number1
DOIs
Publication statusPublished - Jan 2023

Keywords

  • breast cancer
  • HER2 low
  • interobserver agreement

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