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. 2024 Feb 13;30(3):716–729. doi: 10.1038/s41591-024-02808-y

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© The Author(s) 2024

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Extended Data Fig. 4 — Kaplan–Meier analyses of (left) PFS and (right) OS with durvalumab-ceralasertib in patients with a, primary vs acquired resistance, b, PD-L1-negative vs -positive status, and c, squamous cell carcinoma vs non-squamous histology, and in patients d, with or without bone/liver metastases, e, with high or low tumour mutational burden, and according to f, STK11 status and g, KRAS status (variant or wild-type).