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. 2022 Dec 8;28(12):2573–2583. doi: 10.1038/s41591-022-02126-1

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© The Author(s) 2022

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. 3 — Progression-free survival by iRECIST in the subpopulation with high (> 66^th percentile) and low (≤ 66^th percentile) tumor inflammation signature (TIS) in the atezo-chemo (a) and placebo-chemo (b) group. Tumor Inflammation Signature was assessed by analysis of pre-treatment biopsies on the NanoString BC360 assay. All patients in the full analysis set for whom samples were available were included in the analysis (placebo-chemo n = 17, atezo-chemo n = 27). Hazard ratios (HR) with confidence intervals (CI) were calculated using the Cox proportional hazards method.