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. 2021 Apr 1;100(9):2339–2350. doi: 10.1007/s00277-021-04494-z

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© The Author(s) 2021

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 — Survival with first allo-HSCT and preDLI by risk marker constellation at the time of first-dose preDLI. Kaplan–Meier plot and tabulated outcome parameters for the day 100 landmark cohort with preDLI use, stratified as follows: MC/Clin (n=24), includes 22 patients with detection of mixed chimerism (MC) and 2 with individual clinical risk assessment (Clin) at follow-up immediately preceding first-dose preDLI, without genetic risk markers at that time (non-specific risk indicators); Mol/CG ± MC (n=18), includes 17 patients with AML-typical molecular genetic findings (Mol), including 5 with concomitant mixed chimerism, and one with cytogenetic findings (CG), with concomitant mixed chimerism, reported at follow-up immediately preceding first-dose preDLI (leukemia-specific risk indicators). Survival times from day of transplantation