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Mutations of epigenetic modifier genes predict poor outcome in adult acute lymphoblastic leukemia.

Jiawang OuShiyu DengChenhao DingZihong CaiJunjie ChenZicong HuangXiuli XuJia LiZhengwei WuBingqing TangTing ZhangZhixiang WangYa ZhouLi XuanQifa LiuHongsheng Zhou
Published in: Annals of hematology (2024)
Epigenetic modifier (EM) genes play important roles in the occurrence and progression of acute lymphoblastic leukemia (ALL). However, the prognostic significance of EM mutations in ALL has not yet been thoroughly investigated. This retrospective study included 205 adult patients with ALL engaged in a pediatric-type regimen. Based on targeted next-generation sequencing, they were divided into EM mutation group (EM-mut, n = 75) and EM wild-type group (EM-wt, n = 130). The EM-mut group showed a higher positive rate of minimal residual disease (MRD) on treatment day24 and before consolidation therapy (P = 0.026, 0.020). Multivariate Cox regression analysis showed that EM-mut was an independent adverse factor for overall survival (OS) and event-free survival (EFS) (HR = 2.123, 1.742; P = 0.009, 0.007). Survival analysis revealed that the OS and EFS rates were significantly lower in the EM-mut group than in the EM-wt group (3-year OS rate, 45.8% vs. 65.0%, P = 0.0041; 3-year EFS rate, 36.7% vs. 53.2%, P = 0.011). In conclusion, EM was frequently mutated in adult ALL and was characterized by poor response to induction therapy and inferior clinical outcomes.
Keyphrases
  • acute lymphoblastic leukemia
  • free survival
  • dna methylation
  • genome wide
  • risk assessment
  • mass spectrometry
  • high resolution
  • smoking cessation
  • cell therapy
  • chemotherapy induced