首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Prospective evaluation of gene mutations and minimal residual disease in patients with core binding factor acute myeloid leukemia.
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Prospective evaluation of gene mutations and minimal residual disease in patients with core binding factor acute myeloid leukemia.

机译:核心结合因子急性髓细胞白血病患者的基因突变和最小残留疾病的前瞻性评估。

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摘要

Not all patients with core binding factor acute myeloid leukemia (CBF-AML) display a good outcome. Modern risk factors include KIT and/or FLT3 gene mutations and minimal residual disease (MRD) levels, but their respective values have never been prospectively assessed. A total of 198 CBF-AML patients were randomized between a reinforced and a standard induction course, followed by 3 high-dose cytarabine consolidation courses. MRD levels were monitored prospectively. Gene mutations were screened at diagnosis. Despite a more rapid MRD decrease after reinforced induction, induction arm did not influence relapse-free survival (RFS) (64% in both arms; P = .91). Higher WBC, KIT, and/or FLT3-ITD/TKD gene mutations, and a less than 3-log MRD reduction after first consolidation, were associated with a higher specific hazard of relapse, but MRD remained the sole prognostic factor in multivariate analysis. At 36 months, cumulative incidence of relapse and RFS were 22% vs 54% (P < .001) and 73% vs 44% (P < .001) in patients who achieved 3-log MRD reduction vs the others. These results suggest that MRD, rather than gene mutations, should be used for future treatment stratifications in CBF-AML patients. This trial was registered at EudraCT as #2006-005163-26 and at www.clinicaltrials.gov as #NCT 00428558.
机译:并非所有患有核心结合因子急性髓性白血病(CBF-AML)的患者都表现出良好的预后。现代危险因素包括KIT和/或FLT3基因突变以及最小残留疾病(MRD)水平,但从未对其前瞻性评估。总共198名CBF-AML患者被随机分为强化和标准诱导疗程,随后是3个大剂量阿糖胞苷巩固疗程。前瞻性监测MRD水平。在诊断时筛选基因突变。尽管强化诱导后MRD下降较快,但诱导臂并未影响无复发生存期(RFS)(两组均64%; P = 0.91)。较高的WBC,KIT和/或FLT3-ITD / TKD基因突变,以及首次合并后MRD降低少于3 log,与更高的复发特异性危险相关,但MRD仍然是多变量分析的唯一预后因素。在36个月时,MRD降低3对数的患者与其他患者相比,复发和RFS的累积发生率分别为22%vs 54%(P <.001)和73%vs 44%(P <.001)。这些结果表明,应将CRD-AML患者的MRD而不是基因突变用于将来的治疗分层。该试验已在EudraCT上注册为#2006-005163-26,在www.clinicaltrials.gov上注册为#NCT 00428558。

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