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. 2024 Oct 5;8:225. doi: 10.1038/s41698-024-00680-0

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. 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-nc-nd/4.0/.

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Fig. 4 — a Forest plot showing the survival analysis results of six immune cells in TRACERxC1 cohort. The average (Avg.), maximal (Max.), and minimal (Min.) infiltration values of each immune cell were used to obtain the patient-level immune infiltration and then were analyzed with univariate Cox regression. In the Hazard Ratio column, a 95% confidence interval was shown as a dotted line. b The bar graph of the C-index evaluating the same immune cells in the MDAMPLC cohort. The infiltration level of six immune cell types was calculated in all regions of each patient. The minimal infiltration level of Naïve B, Memory B, CD8+ T, and CD4+ T cells (protective) but the maximal infiltration level of Monocyte (hazardous) achieves the highest prognostic association. The survival analysis measures disease-free survival.