Frequency and impact of somatic co-occurring mutations on post-transplant outcomes in acute myeloid leukemia: a multicenter registry analysis on behalf of the EBMT ALWP.

Bazarbachi, Ali;Galimard, Jacques-Emmanuel;Abou Dalle, Iman;Labopin, Myriam;Mohty, Mohamad;et.al.
(2026) Bone Marrow Transplantation — Vol. 61, n° 3, p. 282-293 (2026)

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Authors
  • Bazarbachi, Aliorcid-logo
    Author
  • Galimard, Jacques-Emmanuelorcid-logo
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  • Abou Dalle, Imanorcid-logo
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  • Labopin, Myriamorcid-logo
    Author
  • Poire, XavierUCLouvain
    Author
  • Mohty, Mohamadorcid-logo
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Abstract
(en) Acute myeloid leukemia (AML) includes genetically defined subsets. In allogeneic hematopoietic cell transplantation (allo-HCT), the frequency and prognosis of gene-gene interactions may differ from those of patients treated with chemotherapy alone. In this study, adult patients (N = 952) with AML allografted between 2015 and 2023, with available next generation sequencing (NGS) at diagnosis were included. Most frequent mutations were DNMT3A (24%), FLT3-ITD (21%), NPM1 (21%), RUNX1 (16%), NRAS (16%), TET2 (14%), and IDH2 (12%). Multiple correspondence analysis identified distinct groups of co-occurring mutations. Outcome analysis was performed on 646 AML patients allografted in first complete remission (CR1). Six non-overlapping groups were constructed: 1) TP53 mutation (N = 47); 2) NPM1 mutation (N = 129); 3) FLT3-ITD and/or DNMT3A mutation (N = 128); 4) SRSF2 and/or ASXL1 and/or RUNX1 mutation (SAR group) (N = 132); 5) IDH1 and/or IDH2 and/or TET2 mutation (N = 43); and 6) all ten genes unmutated (N = 167). In multivariable analysis, TP53 mutation, adverse karyotype, and age negatively affected leukemia-free survival (LFS) and overall survival (OS). OS was additionally negatively affected when the ten genes were unmutated. Notably, outcomes were excellent for SAR mutations (2-year LFS 76%, OS 84%), indicating allo-HCT in CR1 can overcome their adverse risk at diagnosis.
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Bazarbachi, A., Galimard, J.-E., Abou Dalle, I., Labopin, M., Sanz, J., Huang, H., Mayer, J., Solano, C., Lioure, B., Griskevicius, L., Maertens, J., Itälä-Remes, M., Kaare, A., Gallego-Hernanz, M.-P., Bug, G., Ribera, J.-M., Gadisseur, A., Schmid, C., Kwon, M., et al. (2026). Frequency and impact of somatic co-occurring mutations on post-transplant outcomes in acute myeloid leukemia: a multicenter registry analysis on behalf of the EBMT ALWP. Bone Marrow Transplantation, 61(3), 282-293. https://doi.org/10.1038/s41409-025-02770-4 (Original work published 2026)