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A multicenter round robin test of PD-L1 expression assessment in urothelial bladder cancer by immunohistochemistry and RT-qPCR with emphasis on prognosis prediction after radical cystectomy
BACKGROUND: Immunohistochemical PD-L1 assessment is currently used to identify responders towards checkpoint inhibitors although it is limited by inter-observer effects. Here, we conducted a multi-center round robin test to prove the possibility of assessing the PD-L1 status by gene expression to av...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871092/ https://www.ncbi.nlm.nih.gov/pubmed/29599921 http://dx.doi.org/10.18632/oncotarget.24531 |
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author | Eckstein, Markus Wirtz, Ralph M. Pfannstil, Carolin Wach, Sven Stoehr, Robert Breyer, Johannes Erlmeier, Franziska Günes, Cagatay Nitschke, Katja Weichert, Wilko Otto, Wolfgang Keck, Bastian Eidt, Sebastian Burger, Maximilian Taubert, Helge Wullich, Bernd Bolenz, Christian Hartmann, Arndt Erben, Philipp |
author_facet | Eckstein, Markus Wirtz, Ralph M. Pfannstil, Carolin Wach, Sven Stoehr, Robert Breyer, Johannes Erlmeier, Franziska Günes, Cagatay Nitschke, Katja Weichert, Wilko Otto, Wolfgang Keck, Bastian Eidt, Sebastian Burger, Maximilian Taubert, Helge Wullich, Bernd Bolenz, Christian Hartmann, Arndt Erben, Philipp |
author_sort | Eckstein, Markus |
collection | PubMed |
description | BACKGROUND: Immunohistochemical PD-L1 assessment is currently used to identify responders towards checkpoint inhibitors although it is limited by inter-observer effects. Here, we conducted a multi-center round robin test to prove the possibility of assessing the PD-L1 status by gene expression to avoid inter-observer effects. PATIENTS AND METHODS: Gene expression of PD-L1 was analyzed in a total of 294 samples (14 cases non-muscle invasive and muscle-invasive bladder cancer; MIBC) in seven centers by a RT-qPCR kit and compared with immunohistochemical scoring of three pathologists (DAKO, 22c3). Both assays were compared towards prognosis prediction in a cohort of 88 patients with MIBC. RESULTS: PD-L1 gene expression revealed very high inter center correlation (centrally extracted RNA: r = 0.68–0.98, p ≤ 0.0076; locally extracted RNA: r = 0.81–0.98, p ≤ 0.0014). IHC Inter-observer concordance was moderate to substantial for immune cells (IC), fair for combined IC/ tumor cell (TC) (IC: κ = 0.50–0.61; IC + TC: κ = 0.50), and fair for TC scoring (κ = 0.26–0.35). Gene expression assessment resulted in more positive cases (9/14 cases positive vs. 6/14 cases [IHC]) which could be validated in the independent cohort. Positive mRNA status was associated with significantly better overall and disease-specific survival (5-year OS: 50% vs. 26%, p = 0.0042, HR = 0.48; 5 year DSS: 65% vs. 40%, p = 0.012, HR = 0.49). The 1% IHC IC cut-off also revealed significant better OS (5 year OS: 58% vs. 31%, p = 0.036, HR = 0.62). CONCLUSION: Gene expression showed very high inter-center agreement. Gene expression assessment also resulted in more positive cases and revealed better prognosis prediction. PD-L1 mRNA expression seems to be a reproducible and robust tool for PD-L1 assessment. |
format | Online Article Text |
id | pubmed-5871092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-58710922018-03-29 A multicenter round robin test of PD-L1 expression assessment in urothelial bladder cancer by immunohistochemistry and RT-qPCR with emphasis on prognosis prediction after radical cystectomy Eckstein, Markus Wirtz, Ralph M. Pfannstil, Carolin Wach, Sven Stoehr, Robert Breyer, Johannes Erlmeier, Franziska Günes, Cagatay Nitschke, Katja Weichert, Wilko Otto, Wolfgang Keck, Bastian Eidt, Sebastian Burger, Maximilian Taubert, Helge Wullich, Bernd Bolenz, Christian Hartmann, Arndt Erben, Philipp Oncotarget Research Paper BACKGROUND: Immunohistochemical PD-L1 assessment is currently used to identify responders towards checkpoint inhibitors although it is limited by inter-observer effects. Here, we conducted a multi-center round robin test to prove the possibility of assessing the PD-L1 status by gene expression to avoid inter-observer effects. PATIENTS AND METHODS: Gene expression of PD-L1 was analyzed in a total of 294 samples (14 cases non-muscle invasive and muscle-invasive bladder cancer; MIBC) in seven centers by a RT-qPCR kit and compared with immunohistochemical scoring of three pathologists (DAKO, 22c3). Both assays were compared towards prognosis prediction in a cohort of 88 patients with MIBC. RESULTS: PD-L1 gene expression revealed very high inter center correlation (centrally extracted RNA: r = 0.68–0.98, p ≤ 0.0076; locally extracted RNA: r = 0.81–0.98, p ≤ 0.0014). IHC Inter-observer concordance was moderate to substantial for immune cells (IC), fair for combined IC/ tumor cell (TC) (IC: κ = 0.50–0.61; IC + TC: κ = 0.50), and fair for TC scoring (κ = 0.26–0.35). Gene expression assessment resulted in more positive cases (9/14 cases positive vs. 6/14 cases [IHC]) which could be validated in the independent cohort. Positive mRNA status was associated with significantly better overall and disease-specific survival (5-year OS: 50% vs. 26%, p = 0.0042, HR = 0.48; 5 year DSS: 65% vs. 40%, p = 0.012, HR = 0.49). The 1% IHC IC cut-off also revealed significant better OS (5 year OS: 58% vs. 31%, p = 0.036, HR = 0.62). CONCLUSION: Gene expression showed very high inter-center agreement. Gene expression assessment also resulted in more positive cases and revealed better prognosis prediction. PD-L1 mRNA expression seems to be a reproducible and robust tool for PD-L1 assessment. Impact Journals LLC 2018-02-19 /pmc/articles/PMC5871092/ /pubmed/29599921 http://dx.doi.org/10.18632/oncotarget.24531 Text en Copyright: © 2018 Eckstein et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Eckstein, Markus Wirtz, Ralph M. Pfannstil, Carolin Wach, Sven Stoehr, Robert Breyer, Johannes Erlmeier, Franziska Günes, Cagatay Nitschke, Katja Weichert, Wilko Otto, Wolfgang Keck, Bastian Eidt, Sebastian Burger, Maximilian Taubert, Helge Wullich, Bernd Bolenz, Christian Hartmann, Arndt Erben, Philipp A multicenter round robin test of PD-L1 expression assessment in urothelial bladder cancer by immunohistochemistry and RT-qPCR with emphasis on prognosis prediction after radical cystectomy |
title | A multicenter round robin test of PD-L1 expression assessment in urothelial bladder cancer by immunohistochemistry and RT-qPCR with emphasis on prognosis prediction after radical cystectomy |
title_full | A multicenter round robin test of PD-L1 expression assessment in urothelial bladder cancer by immunohistochemistry and RT-qPCR with emphasis on prognosis prediction after radical cystectomy |
title_fullStr | A multicenter round robin test of PD-L1 expression assessment in urothelial bladder cancer by immunohistochemistry and RT-qPCR with emphasis on prognosis prediction after radical cystectomy |
title_full_unstemmed | A multicenter round robin test of PD-L1 expression assessment in urothelial bladder cancer by immunohistochemistry and RT-qPCR with emphasis on prognosis prediction after radical cystectomy |
title_short | A multicenter round robin test of PD-L1 expression assessment in urothelial bladder cancer by immunohistochemistry and RT-qPCR with emphasis on prognosis prediction after radical cystectomy |
title_sort | multicenter round robin test of pd-l1 expression assessment in urothelial bladder cancer by immunohistochemistry and rt-qpcr with emphasis on prognosis prediction after radical cystectomy |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871092/ https://www.ncbi.nlm.nih.gov/pubmed/29599921 http://dx.doi.org/10.18632/oncotarget.24531 |
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