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. 2024 Sep 16;14(1):160. doi: 10.1038/s41408-024-01140-5

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© The Author(s) 2024

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/.

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Fig. 3 — A OS within the entire cohort of intensively treated patients: survival with t-AML is inferior to de novo AML. B OS within the entire cohort of non-intensively treated patients: no significant difference between t-AML and de novo AML. C OS of patients with APL: no significant difference between t-APL and de novo APL. D OS of patients with ELN 2010 favorable risk: no significant difference between t-AML and de novo AML. E OS of patients with ELN 2010 intermediate risk: survival with t-AML is inferior to de novo AML. F OS of patients with ELN 2010 adverse risk: survival with t-AML is inferior to de novo AML. n number of patients, OS overall survival, t-AML therapy-related AML, APL acute promyelocytic leukemia, ELN European LeukemiaNet.