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. 2021 Jan 6;19:22. doi: 10.1186/s12967-020-02679-0

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© The Author(s) 2021

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. 3 — The mutation status of FGFR4 is closely associated with the prognosis of NSCLC. a The prevalence of FGFR4 mutations in NSCLC patients based on the cBioPortal for Cancer Genomics; b the expression of FGFR4 was closely related to the prognosis of lung cancer patients; c the mutation status of FGFR4 is associated with the TMB level in TCGA cohort; d the mutation status of FGFR4 is associated with the TMB level in cBioPortal for Cancer Genomics; e the mutation status of FGFR4 is associated with the PD-L1 expression in cBioPortal for Cancer Genomics; f the mutation status of FGFR4 is associated with the PFS of ICIs treatment in cBioPortal for Cancer Genomics