Department of Hematology and Lymphoma Research Center, Peking University, Third Hospital, 49 Huayuan North Road, Beijing, 100191, China.
Department of Biomedical Engineering, Chinese PLA General Hospital, Beijing, 100853, China.
Ann Hematol. 2018 Aug;97(8):1391-1397. doi: 10.1007/s00277-018-3331-8. Epub 2018 Apr 25.
Brain and acute leukemia, cytoplasmic (BAALC) and ETS-related gene (ERG) expression levels are independent prognostic factors for acute myeloid leukemia (AML); however, their prognostic impacts on AML patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) require further investigation. We studied 71 de novo AML patients treated with allo-HSCT and defined low and high expressers according to the median expression levels of BAALC and ERG at diagnosis respectively. High BAALC expression was associated with wild-type NPM1 (P = 0.000) and RUNX1 mutations (P = 0.027). High ERG expression was associated with FLT3-ITD absence (P = 0.003) and wild-type NPM1 (P = 0.001). BAALC and ERG expression levels were significantly correlated with each other (P = 0.001). Survival analyses including Kaplan-Meier curves and univariate and multivariate analysis consistently reported that there were no significant differences for both event-free survival (EFS) and overall survival (OS) (all P > 0.1), between high versus low BAALC and ERG expressers. Our study suggested that despite of their well-known adverse role in prognosis of AML, neither BAALC nor ERG expression levels at diagnosis had effect on survival of AML patients who underwent allo-HSCT.
脑和急性白血病,细胞质(BAALC)和 ETS 相关基因(ERG)的表达水平是急性髓系白血病(AML)的独立预后因素;然而,它们对接受异基因造血干细胞移植(allo-HSCT)的 AML 患者的预后影响仍需要进一步研究。我们研究了 71 例接受 allo-HSCT 治疗的初发 AML 患者,并根据诊断时 BAALC 和 ERG 的中位表达水平分别定义低表达者和高表达者。高 BAALC 表达与野生型 NPM1(P = 0.000)和 RUNX1 突变(P = 0.027)相关。高 ERG 表达与 FLT3-ITD 缺失(P = 0.003)和野生型 NPM1(P = 0.001)相关。BAALC 和 ERG 的表达水平呈显著正相关(P = 0.001)。包括 Kaplan-Meier 曲线和单因素及多因素分析在内的生存分析报告显示,高表达者与低表达者之间在无事件生存(EFS)和总生存(OS)方面均无显著差异(均 P > 0.1)。我们的研究表明,尽管 BAALC 和 ERG 在 AML 预后中具有已知的不良作用,但诊断时它们的表达水平对接受 allo-HSCT 的 AML 患者的生存无影响。