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PD-L1 (SP142) testing is concordant between Benchmark Ultra and Bond-III stainers
BACKGROUND: Atezolizumab is an inhibitor of programmed death-ligand 1 (PD-L1), used to treat advanced or metastatic bladder cancer, and in trials for non-invasive disease. In order to be eligible for treatment, patients require a PD-L1 immune cell score ≥ 5%, using the Ventana SP142 PD-L1 assay. Man...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571218/ https://www.ncbi.nlm.nih.gov/pubmed/34515825 http://dx.doi.org/10.1007/s00345-021-03828-w |
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author | Compérat, Eva Oszwald, André Wasinger, Gabriel Wacquet, Justine Rouprêt, Morgan Cussenot, Olivier |
author_facet | Compérat, Eva Oszwald, André Wasinger, Gabriel Wacquet, Justine Rouprêt, Morgan Cussenot, Olivier |
author_sort | Compérat, Eva |
collection | PubMed |
description | BACKGROUND: Atezolizumab is an inhibitor of programmed death-ligand 1 (PD-L1), used to treat advanced or metastatic bladder cancer, and in trials for non-invasive disease. In order to be eligible for treatment, patients require a PD-L1 immune cell score ≥ 5%, using the Ventana SP142 PD-L1 assay. Many laboratories do not have access to the required Ventana Benchmark Ultra stainer, and it is unclear if the assay performs similarly on other stainers. In this study, we compare SP142 assay results between Ventana Benchmark Ultra and Leica Bond-III stainers. METHODS: Serial sections of 90 samples of transurethral bladder resections (comprising 51 pTaHG, 8 pTis, 18 pT1, 10 pT2 tumors) were stained using the SP142 PD-L1 antibody on Ventana Benchmark Ultra and Leica Bond-III stainers, manually scored, and compared using accuracy and Cohen’s kappa measures. RESULTS: Both devices yielded highly concordant PD-L1 immune cell scores (accuracy 0.84, Cohen’s κ 0.732). Moreover, we found similar tumor cell (TC) PD-L1 scores using both stainers, and a trend towards greater TC scores in pT2 stage samples (p = 0.05). CONCLUSION: This study is the first to compare the SP142 antibody in bladder cancer on two different stainers. Our results indicate that both Benchmark Ultra and Bond-III stainers yield highly concordant results using the SP142 PD-L1 antibody. |
format | Online Article Text |
id | pubmed-8571218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-85712182021-11-08 PD-L1 (SP142) testing is concordant between Benchmark Ultra and Bond-III stainers Compérat, Eva Oszwald, André Wasinger, Gabriel Wacquet, Justine Rouprêt, Morgan Cussenot, Olivier World J Urol Topic Paper BACKGROUND: Atezolizumab is an inhibitor of programmed death-ligand 1 (PD-L1), used to treat advanced or metastatic bladder cancer, and in trials for non-invasive disease. In order to be eligible for treatment, patients require a PD-L1 immune cell score ≥ 5%, using the Ventana SP142 PD-L1 assay. Many laboratories do not have access to the required Ventana Benchmark Ultra stainer, and it is unclear if the assay performs similarly on other stainers. In this study, we compare SP142 assay results between Ventana Benchmark Ultra and Leica Bond-III stainers. METHODS: Serial sections of 90 samples of transurethral bladder resections (comprising 51 pTaHG, 8 pTis, 18 pT1, 10 pT2 tumors) were stained using the SP142 PD-L1 antibody on Ventana Benchmark Ultra and Leica Bond-III stainers, manually scored, and compared using accuracy and Cohen’s kappa measures. RESULTS: Both devices yielded highly concordant PD-L1 immune cell scores (accuracy 0.84, Cohen’s κ 0.732). Moreover, we found similar tumor cell (TC) PD-L1 scores using both stainers, and a trend towards greater TC scores in pT2 stage samples (p = 0.05). CONCLUSION: This study is the first to compare the SP142 antibody in bladder cancer on two different stainers. Our results indicate that both Benchmark Ultra and Bond-III stainers yield highly concordant results using the SP142 PD-L1 antibody. Springer Berlin Heidelberg 2021-09-13 2021 /pmc/articles/PMC8571218/ /pubmed/34515825 http://dx.doi.org/10.1007/s00345-021-03828-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Topic Paper Compérat, Eva Oszwald, André Wasinger, Gabriel Wacquet, Justine Rouprêt, Morgan Cussenot, Olivier PD-L1 (SP142) testing is concordant between Benchmark Ultra and Bond-III stainers |
title | PD-L1 (SP142) testing is concordant between Benchmark Ultra and Bond-III stainers |
title_full | PD-L1 (SP142) testing is concordant between Benchmark Ultra and Bond-III stainers |
title_fullStr | PD-L1 (SP142) testing is concordant between Benchmark Ultra and Bond-III stainers |
title_full_unstemmed | PD-L1 (SP142) testing is concordant between Benchmark Ultra and Bond-III stainers |
title_short | PD-L1 (SP142) testing is concordant between Benchmark Ultra and Bond-III stainers |
title_sort | pd-l1 (sp142) testing is concordant between benchmark ultra and bond-iii stainers |
topic | Topic Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571218/ https://www.ncbi.nlm.nih.gov/pubmed/34515825 http://dx.doi.org/10.1007/s00345-021-03828-w |
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