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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
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.
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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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