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Concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma

BACKGROUND: Antibodies targeting the programmed cell death-1 (PD-1)/PD-ligand 1 (PD-1/PD-L1) checkpoint have shown promising clinical activity in patients with advanced urothelial carcinoma (UC). Expression of PD-L1 in UC tumors has been investigated using different antibody clones, staining protoco...

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Autores principales: Zajac, Magdalena, Scott, Marietta, Ratcliffe, Marianne, Scorer, Paul, Barker, Craig, Al-Masri, Hytham, Rebelatto, Marlon C., Walker, Jill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720992/
https://www.ncbi.nlm.nih.gov/pubmed/31477145
http://dx.doi.org/10.1186/s13000-019-0873-6
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author Zajac, Magdalena
Scott, Marietta
Ratcliffe, Marianne
Scorer, Paul
Barker, Craig
Al-Masri, Hytham
Rebelatto, Marlon C.
Walker, Jill
author_facet Zajac, Magdalena
Scott, Marietta
Ratcliffe, Marianne
Scorer, Paul
Barker, Craig
Al-Masri, Hytham
Rebelatto, Marlon C.
Walker, Jill
author_sort Zajac, Magdalena
collection PubMed
description BACKGROUND: Antibodies targeting the programmed cell death-1 (PD-1)/PD-ligand 1 (PD-1/PD-L1) checkpoint have shown promising clinical activity in patients with advanced urothelial carcinoma (UC). Expression of PD-L1 in UC tumors has been investigated using different antibody clones, staining protocols, and scoring algorithms. The aim was to establish the extent of concordance among PD-L1 immunohistochemistry (IHC) assays. METHODS: Tumor biopsy samples (N = 335) were assessed using four commercially available PD-L1 assays: VENTANA SP263, VENTANA SP142, PD-L1 IHC 28–8 pharmDx, and PD-L1 IHC 22C3 pharmDx. PD-L1 analytical staining and classification concordance, including agreement between clinically relevant scoring algorithms, were investigated using overall/positive/negative percentage agreement (OPA/PPA/NPA). RESULTS: Good analytical correlation was observed among the VENTANA SP263, PD-L1 IHC 22C3 pharmDx, and PD-L1 IHC 28–8 pharmDx assays for tumor cell (TC) and immune cell (IC) PD-L1 staining with Spearman rank coefficients of 0.92–0.93 for TCs and 0.88–0.91 for ICs. However, concordance (preset criterion: ≥85%) between patient PD-L1 status when applying the TC or IC(ICArea) ≥ 25% (VENTANA SP263) cutoff was only achieved for PD-L1 IHC 22C3 pharmDx versus VENTANA SP263 (OPA 92.2%, PPA 86.4%, NPA 95.4%). Differences were observed between patient populations with UC tumors classified as PD-L1 high versus PD-L1 low/negative using combined positive score (CPS) ≥1, CPS ≥10, IC ≥5%, and TC/IC ≥25%. CONCLUSIONS: The VENTANA SP263 and PD-L1 IHC 22C3 pharmDx assays are analytically similar in UC. When the different PD-L1 assays were combined with their specified clinical scoring algorithms, differences were seen in patient classification driven by substantial differences in scoring approaches. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13000-019-0873-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-67209922019-09-10 Concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma Zajac, Magdalena Scott, Marietta Ratcliffe, Marianne Scorer, Paul Barker, Craig Al-Masri, Hytham Rebelatto, Marlon C. Walker, Jill Diagn Pathol Research BACKGROUND: Antibodies targeting the programmed cell death-1 (PD-1)/PD-ligand 1 (PD-1/PD-L1) checkpoint have shown promising clinical activity in patients with advanced urothelial carcinoma (UC). Expression of PD-L1 in UC tumors has been investigated using different antibody clones, staining protocols, and scoring algorithms. The aim was to establish the extent of concordance among PD-L1 immunohistochemistry (IHC) assays. METHODS: Tumor biopsy samples (N = 335) were assessed using four commercially available PD-L1 assays: VENTANA SP263, VENTANA SP142, PD-L1 IHC 28–8 pharmDx, and PD-L1 IHC 22C3 pharmDx. PD-L1 analytical staining and classification concordance, including agreement between clinically relevant scoring algorithms, were investigated using overall/positive/negative percentage agreement (OPA/PPA/NPA). RESULTS: Good analytical correlation was observed among the VENTANA SP263, PD-L1 IHC 22C3 pharmDx, and PD-L1 IHC 28–8 pharmDx assays for tumor cell (TC) and immune cell (IC) PD-L1 staining with Spearman rank coefficients of 0.92–0.93 for TCs and 0.88–0.91 for ICs. However, concordance (preset criterion: ≥85%) between patient PD-L1 status when applying the TC or IC(ICArea) ≥ 25% (VENTANA SP263) cutoff was only achieved for PD-L1 IHC 22C3 pharmDx versus VENTANA SP263 (OPA 92.2%, PPA 86.4%, NPA 95.4%). Differences were observed between patient populations with UC tumors classified as PD-L1 high versus PD-L1 low/negative using combined positive score (CPS) ≥1, CPS ≥10, IC ≥5%, and TC/IC ≥25%. CONCLUSIONS: The VENTANA SP263 and PD-L1 IHC 22C3 pharmDx assays are analytically similar in UC. When the different PD-L1 assays were combined with their specified clinical scoring algorithms, differences were seen in patient classification driven by substantial differences in scoring approaches. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13000-019-0873-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-09-02 /pmc/articles/PMC6720992/ /pubmed/31477145 http://dx.doi.org/10.1186/s13000-019-0873-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zajac, Magdalena
Scott, Marietta
Ratcliffe, Marianne
Scorer, Paul
Barker, Craig
Al-Masri, Hytham
Rebelatto, Marlon C.
Walker, Jill
Concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma
title Concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma
title_full Concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma
title_fullStr Concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma
title_full_unstemmed Concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma
title_short Concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma
title_sort concordance among four commercially available, validated programmed cell death ligand-1 assays in urothelial carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720992/
https://www.ncbi.nlm.nih.gov/pubmed/31477145
http://dx.doi.org/10.1186/s13000-019-0873-6
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