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. 2023 Nov 19;23:281. doi: 10.1186/s12935-023-03122-2

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© The Author(s) 2023

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 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. 5 — Co-mutations in TP53 and ARID1A are associated with inferior clinical outcomes after CAR-T cell therapy. (a) Analysis of co-mutations in r/r MB-NHL. (b) Comparison of response rates of CAR-T cell therapy according to TP53 and ARID1A mutation status. (c) Survival analyses by Kaplan–Meier according to mutation status in patients treated with CAR-T cell therapy