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. 2023 Oct 30;11(10):e007047. doi: 10.1136/jitc-2023-007047

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© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/.

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(A) Prevalence of patients identified in the programmed death-ligand 1 (PD-L1)-negative, PD-L1-positive, and PD-L1-high subgroups among the patients with stage II–IIIA NSCLC in the combined-biomarker-evaluable population (BEP) according to the SP263 assay or among the 22C3-BEP according to the 22C3 assay. (B) Venn diagrams show the percentage of patients in the stage II–IIIA combined-BEP that were defined as having tumors that were PD-L1 positive or PD-L1 high according to both, just one, or neither of the SP263 and 22C3 assays. TC, tumor cell; TPS, tumor proportion score.