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The pathogenesis of therapy-related myeloid neoplasms from TP53-mutant clonal hematopoiesis.

Leukemia 2026 Vol.40(2) p. 279-292

Fullin J, Topçu E, Zielińska KA, Schimmer RR, Klemm N, Koch C, Caiado F, Lock M, Doerdelmann C, Bühler MM, Tchinda J, Kurppa KJ, Borsig L, Jones PH, Lopes M, Manz MG, Boettcher S

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Therapy-related acute myeloid leukemia and myelodysplastic neoplasms (t-AML/MDS) are devastating complications of chemo- or radiation therapy in patients treated for an unrelated primary malignancy.

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APA Fullin J, Topçu E, et al. (2026). The pathogenesis of therapy-related myeloid neoplasms from TP53-mutant clonal hematopoiesis.. Leukemia, 40(2), 279-292. https://doi.org/10.1038/s41375-025-02839-5
MLA Fullin J, et al.. "The pathogenesis of therapy-related myeloid neoplasms from TP53-mutant clonal hematopoiesis.." Leukemia, vol. 40, no. 2, 2026, pp. 279-292.
PMID 41407825

Abstract

Therapy-related acute myeloid leukemia and myelodysplastic neoplasms (t-AML/MDS) are devastating complications of chemo- or radiation therapy in patients treated for an unrelated primary malignancy. Cancer patients with TP53-mutant hematopoietic stem and progenitor cells (HSPCs) - a condition termed clonal hematopoiesis (CH) - are at a particularly high risk for t-AML/MDS. However, the pathogenesis of TP53-mutant t-AML/MDS, especially the role of the TP53 allelic state (i.e., mono- vs. biallelic), and its prognostic impact in AML/MDS have remained only poorly understood. We developed novel in vitro and in vivo mouse models to investigate how mono- or biallelic Trp53 mutations influence clonal expansion and leukemic progression from CH to t-AML/MDS. While HSPCs with monoallelic Trp53 mutations gain clonal fitness but retain their genomic integrity under chemo- or radiation therapy, biallelic Trp53 mutations result in genomic instability and are essential for leukemic transformation. Moreover, we provide proof of concept that non-mutational p53 inactivation, such as MDM2 overexpression, can replicate the effects of biallelic TP53 mutations, providing a possible explanation for cases of TP53-mutant AML/MDS that retain one wild-type TP53 allele. Our findings elucidate the pathogenesis of TP53-mutant t-AML/MDS and support the classification of biallelic TP53-mutant AML/MDS as distinct clinical entities.

MeSH Terms

Animals; Clonal Hematopoiesis; Tumor Suppressor Protein p53; Mice; Mutation; Humans; Leukemia, Myeloid, Acute; Myelodysplastic Syndromes; Neoplasms, Second Primary; Hematopoietic Stem Cells; Genomic Instability; Disease Models, Animal