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- Botling, Johan2
- Bubendorf, Lukas2
- Chen, Gang2
- Chung, Jin-Haeng2
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- Hirsch, Fred R2
- Kerr, Keith M2
- Lantuejoul, Sylvie2
- Mino-Kenudson, Mari2
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- Noguchi, Masayuki2
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- Beasley, Mary Beth1
- Beasley, Mary-Beth1
- Borczuk, Alain1
- Borczuk, Alain C1
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Editors Choice
2 Results
- Original Article Translational OncologyOpen Archive
The International Association for the Study of Lung Cancer Global Survey on Programmed Death-Ligand 1 Testing for NSCLC
Journal of Thoracic OncologyVol. 16Issue 4p686–696Published online: March 1, 2021- Mari Mino-Kenudson
- Nolwenn Le Stang
- Jillian B. Daigneault
- Andrew G. Nicholson
- Wendy A. Cooper
- Anja C. Roden
- and others
Cited in Scopus: 7Programmed death-ligand 1 (PD-L1) immunohistochemistry (IHC) is required to determine the eligibility for pembrolizumab monotherapy in advanced NSCLC worldwide and for several other indications depending on the country. Four assays have been approved/ Communauté Européene–In vitro Diagnostic (CV-IVD)–marked, but PD-L1 IHC seems diversely implemented across regions and laboratories with the application of laboratory-developed tests (LDTs). - Original Article Translational OncologyOpen Archive
PD-L1 Immunohistochemistry Comparability Study in Real-Life Clinical Samples: Results of Blueprint Phase 2 Project
Journal of Thoracic OncologyVol. 13Issue 9p1302–1311Published online: May 22, 2018- Ming Sound Tsao
- Keith M. Kerr
- Mark Kockx
- Mary-Beth Beasley
- Alain C. Borczuk
- Johan Botling
- and others
Cited in Scopus: 482The 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.