The Impact of Mutation of Myelodysplasia-Related Genes in De Novo Acute Myeloid Leukemia Carrying NPM1 Mutation.
Yi WangAndrés E QuesadaZhuang ZuoL Jeffrey MedeirosCheng Cameron YinShaoying LiJie XuGautam BorthakurYisheng LiChao YangYasmin M AbazaJuehua GaoXinyan LuM James YouYizhuo ZhangPei LinPublished in: Cancers (2022)
Background: The impact of gene mutations typically associated with myelodysplastic syndrome (MDS) in acute myeloid leukemia (AML) with NPM1 mutation is unclear. Methods: Using a cohort of 107 patients with NPM1-mutated AML treated with risk-adapted therapy, we compared survival outcomes of patients without MDS-related gene mutations (group A) with those carrying concurrent FLT3-ITD (group B) or with MDS-related gene mutations (group C). Minimal measurable disease (MMD) status assessed by multiparameter flow cytometry (MFC), polymerase chain reaction (PCR), and/or next-generation sequencing (NGS) were reviewed. Results: Among the 69 patients treated intensively, group C showed significantly inferior progression-free survival (PFS, p < 0.0001) but not overall survival (OS, p = 0.055) compared to group A. Though groups A and C had a similar MMD rate, group C patients had a higher relapse rate (p = 0.016). Relapse correlated with MMD status at the end of cycle 2 induction (p = 0.023). Survival of group C patients was similar to that of group B. Conclusion: MDS-related gene mutations are associated with an inferior survival in NPM1-mutated AML.
Keyphrases
- acute myeloid leukemia
- free survival
- end stage renal disease
- newly diagnosed
- allogeneic hematopoietic stem cell transplantation
- ejection fraction
- flow cytometry
- chronic kidney disease
- peritoneal dialysis
- prognostic factors
- stem cells
- gene expression
- radiation therapy
- genome wide
- bone marrow
- tyrosine kinase
- patient reported
- patient reported outcomes