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. 2022 Jun 23;22:691. doi: 10.1186/s12885-022-09755-2

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© The Author(s) 2022

Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 1 — Prognostic risk models constructed by four immune-related signatures for overall survival (OS) in early and advanced RCC. A Classified efficiency of prognostic risk models constructed by four immune-related signatures (IFN-gamma signature, extended immune gene signature, cytotoxic T lymphocyte signature and HLA-A and HLA-B) in stage I + II RCC. B Classified efficiency of the four prognostic risk models for stage III + IV RCC. The p-value was shown in the survival plots