A multicentre analytical comparison study of inter-reader and inter-assay agreement of four programmed death-ligand 1 immunohistochemistry assays for scoring in triple-negative breast cancer.

Noske, Aurelia; Ammann, Johannes U; Wagner, Daniel-Christoph; Denkert, Carsten; Lebeau, Annette; Sinn, Peter; Kreipe, Hans-Heinrich; Sommer, Ulrich; Baretton, Gustavo; Steiger, Katja; Kiechle, Marion; Hieke-Schulz, Stefanie; Flores, Mike; Roth, Wilfried; Weichert, Wilko

doi:10.1111/his.14254

Benutzer: Gast

journal article

Dokumenttyp:: Journal Article
Autor(en):: Noske, Aurelia; Ammann, Johannes U; Wagner, Daniel-Christoph; Denkert, Carsten; Lebeau, Annette; Sinn, Peter; Kreipe, Hans-Heinrich; Sommer, Ulrich; Baretton, Gustavo; Steiger, Katja; Kiechle, Marion; Hieke-Schulz, Stefanie; Flores, Mike; Roth, Wilfried; Weichert, Wilko
Titel:: A multicentre analytical comparison study of inter-reader and inter-assay agreement of four programmed death-ligand 1 immunohistochemistry assays for scoring in triple-negative breast cancer.
Abstract:: AIMS: Studies in various cancer types have demonstrated discordance between results from different programmed death-ligand 1 (PD-L1) assays. Here, we compare the reproducibility and analytical concordance of four clinically developed assays for assessing PD-L1-positivity in tumour-infiltrating immune cells in the tumour area (PD-L1-IC-positivity) in triple-negative breast cancer (TNBC). METHODS AND RESULTS: Primary TNBC resection specimens (n = 30) were selected based on their PD-L1-IC-positivity per VENTANA SP142 (<1%: 15 cases; 1-5%: seven cases; >5%: eight cases). Serial histological sections were stained for PD-L1 using VENTANA SP142, VENTANA SP263, DAKO 22C3 and DAKO 28-8. PD-L1-IC-positivity and tumour cell expression (≥1 versus <1%) were scored by trained readers from seven sites using online virtual microscopy. The adjusted mean of PD-L1-IC-positivity for SP263 (7.8%) was significantly higher than those for the other three assays (3.7-4.9%). Differences in adjusted means were statistically significant between SP263 and the other three assays (P < 0.0001) but not between the three remaining assays when excluding SP263 (P = 0.0961-0.6522). Intra-class correlation coefficients revealed moderate-to-strong inter-reader agreement for each assay (0.460-0.805) and poor-to-strong inter-assay agreement for each reader (0.298-0.678) on PD-L1-IC-positivity. CONCLUSIONS: In this first multicentre study of different PD-L1 assays in TNBC, we show that PD-L1-IC-positivity for SP142, 22C3 and 28-8 was reproducible and analytically concordant, indicating that these three assays may be analytically interchangeable. The relevance of the higher PD-L1-IC-positivity for SP263 should be further investigated.
Zeitschriftentitel:: Histopathology
Jahr:: 2021
Band / Volume:: 78
Heft / Issue:: 4
Seitenangaben Beitrag:: 567-577
Volltext / DOI:: doi:10.1111/his.14254
PubMed:: http://view.ncbi.nlm.nih.gov/pubmed/32936950
Print-ISSN:: 0309-0167
TUM Einrichtung:: Frauenklinik und Poliklinik; Institut für Allgemeine Pathologie und Pathologische Anatomie
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