Monitoring Immunohistochemical Staining Variations Using Artificial Intelligence on Standardized Controls

Sven van Kempen1, W J Ghlowy Gerritsen1, Tri Q Nguyen1

  • 1Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

Insights

Artificial intelligence (AI) effectively monitors immunohistochemistry (IHC) stain quality using standardized cell lines for HER2 and PD-L1. AI identifies variations in staining, crucial for accurate patient management and quality control in pathology.

Area of Science:

  • Pathology
  • Biotechnology
  • Artificial Intelligence

Background:

  • Immunohistochemistry (IHC) quality control is vital for patient management.
  • Traditional control tissues face limitations due to scarcity and heterogeneity.
  • Standardized cell lines offer a promising alternative for IHC quality control.

Purpose of the Study:

  • To investigate the use of artificial intelligence (AI) for monitoring the IHC stain quality of standardized cell lines.
  • To evaluate AI-based quality control for HER2 and PD-L1 IHC staining.
  • To identify and trace variations in IHC staining using AI.

Main Methods:

  • Utilized standardized cell lines for HER2 and PD-L1 IHC staining across five autostainers.
  • Employed Qualitopix, an AI algorithm, for quantitative measurement of cell membrane expression and stain quality over 24 months.
  • Assessed inter-stainer and intra-run variations, and determined the limit of detection for variance.

Main Results:

  • Observed unexpected variations in AI-measured stain quality, especially in low- and medium-expressing cell lines.
  • Identified significant differences between autostainers and within slide slots.
  • Maintenance on a fluctuating stainer reduced observed variations.

Conclusions:

  • AI is an effective tool for monitoring IHC stain quality of standardized control cell lines.
  • AI facilitates the detection and tracing of errors in IHC staining processes.
  • AI-driven quality control is crucial for ensuring accurate patient management in targeted therapies like HER2 and PD-L1.