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. 2023 Nov 11;14:7301. doi: 10.1038/s41467-023-42900-4

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — *Most common reasons were patients not meeting the inclusion criteria for confirmed metastatic non-squamous NSCLC with documented absence of genomic aberration with available approved target therapy (n = 24) and for documented PD-L1 status by the 22C3 pharmDx assay (n = 22). ^†Other reasons included death (n = 4) and lost to follow-up (n = 1). ^‡Pemetrexed plus platinum-based therapy (either cisplatin or carboplatin). CONSORT Consolidated Standards of Reporting Trials, NSCLC non-small cell lung cancer, PD-L1 programmed death ligand 1.