Prognostic impact of myelodysplasia-related gene mutations in ELN-2022 favorable-risk acute myeloid leukemia subtypes.
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Acute Myeloid Leukemia Research
Chronic Myeloid Leukemia Treatments
Retinoids in leukemia and cellular processes
[BACKGROUND] The 2022 European Leukemia Net (ELN) risk stratification categorizes acute myeloid leukemia (AML) with myelodysplasia-related gene (MRG) mutations - including , , , , , , , and/or - as
APA
Lulu Zhang, Shuangwei Ying, et al. (2026). Prognostic impact of myelodysplasia-related gene mutations in ELN-2022 favorable-risk acute myeloid leukemia subtypes.. Annals of medicine, 58(1), 2636337. https://doi.org/10.1080/07853890.2026.2636337
MLA
Lulu Zhang, et al.. "Prognostic impact of myelodysplasia-related gene mutations in ELN-2022 favorable-risk acute myeloid leukemia subtypes.." Annals of medicine, vol. 58, no. 1, 2026, pp. 2636337.
PMID
41797681
Abstract
[BACKGROUND] The 2022 European Leukemia Net (ELN) risk stratification categorizes acute myeloid leukemia (AML) with myelodysplasia-related gene (MRG) mutations - including , , , , , , , and/or - as "adverse-risk". However, the prognostic relevance of MRG mutations in patients with favorable-risk AML remains uncertain.
[METHODS] In this study, we analyzed a cohort of 221 adult patients with de novo favorable-risk AML. Risk groups were classified according to the 2022 European Leukemia Net guideline.
[RESULTS] A total of 47 AML patients (21.3%) harbored MRG mutations. The presence of MRG mutations was associated with older age (57 vs. 49, = 0.005), lower white blood cell count (6.9 vs. 14.5, = 0.015), and the presence of (27.7% vs. 10.9%, = 0.004), (6.4% vs. 0.6%, = 0.031), and (6.4% vs. 1.1%, = 0.066) mutations. Our findings indicated that the presence of MRG mutations did not significantly impact 2-year overall survival (OS) (75.2% vs. 69.4%, = 0.285) or leukemia-free survival (LFS) (58.9% vs. 52.5%, = 0.640). However, patients with two or more MRG mutations had significantly poorer LFS than those with one MRG mutation ( = 0.004) or without MRG mutations ( = 0.001). By multivariable analysis, ≥2 MRG mutations was independently associated with worse LFS.
[CONCLUSION] The presence of a single MRG mutation did not confer a worse prognosis in favorable-risk AML, whereas a high MRG mutation burden (≥2 mutations) was independently associated with poorer LFS. This study suggests that quantifying the MRG mutation burden may inform risk stratification in this patient population.
[METHODS] In this study, we analyzed a cohort of 221 adult patients with de novo favorable-risk AML. Risk groups were classified according to the 2022 European Leukemia Net guideline.
[RESULTS] A total of 47 AML patients (21.3%) harbored MRG mutations. The presence of MRG mutations was associated with older age (57 vs. 49, = 0.005), lower white blood cell count (6.9 vs. 14.5, = 0.015), and the presence of (27.7% vs. 10.9%, = 0.004), (6.4% vs. 0.6%, = 0.031), and (6.4% vs. 1.1%, = 0.066) mutations. Our findings indicated that the presence of MRG mutations did not significantly impact 2-year overall survival (OS) (75.2% vs. 69.4%, = 0.285) or leukemia-free survival (LFS) (58.9% vs. 52.5%, = 0.640). However, patients with two or more MRG mutations had significantly poorer LFS than those with one MRG mutation ( = 0.004) or without MRG mutations ( = 0.001). By multivariable analysis, ≥2 MRG mutations was independently associated with worse LFS.
[CONCLUSION] The presence of a single MRG mutation did not confer a worse prognosis in favorable-risk AML, whereas a high MRG mutation burden (≥2 mutations) was independently associated with poorer LFS. This study suggests that quantifying the MRG mutation burden may inform risk stratification in this patient population.
MeSH Terms
Humans; Male; Female; Leukemia, Myeloid, Acute; Middle Aged; Mutation; Prognosis; Aged; Adult; Myelodysplastic Syndromes; Aged, 80 and over; Risk Assessment; Young Adult; Risk Factors
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