PD-L1 immunohistochemistry comparability study in real-life clinical samples: Results of Blueprint phase 2 project Journal Article


Authors: Tsao, M. S.; Kerr, K. M.; Kockx, M.; Beasley, M. B.; Borczuk, A. C.; Botling, J.; Bubendorf, L.; Chirieac, L.; Chen, G.; Chou, T. Y.; Chung, J. H.; Dacic, S.; Lantuejoul, S.; Mino-Kenudson, M.; Moreira, A. L.; Nicholson, A. G.; Noguchi, M.; Pelosi, G.; Poleri, C.; Russell, P. A.; Sauter, J.; Thunnissen, E.; Wistuba, I.; Yu, H.; Wynes, M. W.; Pintilie, M.; Yatabe, Y.; Hirsch, F. R.
Article Title: PD-L1 immunohistochemistry comparability study in real-life clinical samples: Results of Blueprint phase 2 project
Abstract: Objectives: The Blueprint (BP) Programmed Death Ligand 1 (PD-L1) Immunohistochemistry Comparability Project is a pivotal academic/professional society and industrial collaboration to assess the feasibility of harmonizing the clinical use of five independently developed commercial PD-L1 immunohistochemistry assays. The goal of BP phase 2 (BP2) was to validate the results obtained in BP phase 1 by using real-world clinical lung cancer samples. Methods: BP2 were conducted using 81 lung cancer specimens of various histological and sample types, stained with all five trial-validated PD-L1 assays (22C3, 28-8, SP142, SP263, and 73-10); the slides were evaluated by an international panel of pathologists. BP2 also assessed the reliability of PD-L1 scoring by using digital images, and samples prepared for cytological examination. PD-L1 expression was assessed for percentage (tumor proportional score) of tumor cell (TC) and immune cell areas showing PD-L1 staining, with TCs scored continuously or categorically with the cutoffs used in checkpoint inhibitor trials. Results: The BP2 results showed highly comparable staining by the 22C3, 28-8 and SP263 assays; less sensitivity with the SP142 assay; and higher sensitivity with the 73-10 assay to detect PD-L1 expression on TCs. Glass slide and digital image scorings were highly concordant (Pearson correlation >0.96). There was very strong reliability among pathologists in TC PD-L1 scoring with all assays (overall intraclass correlation coefficient [ICC] = 0.86–0.93), poor reliability in IC PD-L1 scoring (overall ICC = 0.18–0.19), and good agreement in assessing PD-L1 status on cytological cell block materials (ICC = 0.78–0.85). Conclusion: BP2 consolidates the analytical evidence for interchangeability of the 22C3, 28-8, and SP263 assays and lower sensitivity of the SP142 assay for determining tumor proportion score on TCs and demonstrates greater sensitivity of the 73-10 assay compared with that of the other assays. © 2018 International Association for the Study of Lung Cancer
Keywords: cytology; pathology; companion diagnostics; checkpoint inhibitors; immunooncology; complementary diagnostics
Journal Title: Journal of Thoracic Oncology
Volume: 13
Issue: 9
ISSN: 1556-0864
Publisher: Elsevier Inc.  
Date Published: 2018-09-01
Start Page: 1302
End Page: 1311
Language: English
DOI: 10.1016/j.jtho.2018.05.013
PROVIDER: scopus
PUBMED: 29800747
PMCID: PMC8386299
DOI/URL:
Notes: Article -- Export Date: 4 September 2018 -- Source: Scopus
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  1. Jennifer Lynn Sauter
    124 Sauter