Department of Hematology, Huaihe Hospital of Henan University, Kaifeng 475000, China.
Department of Hematology, The first Affiliated Hospital of Henan University, Kaifeng 475000, China.
Biosci Rep. 2020 Jun 26;40(6). doi: 10.1042/BSR20200097.
The purpose of the present study was to investigate whether expression levels of adenylate kinase 1 (AK1) were associated with prognosis of acute myeloid leukemia (AML) in patients treated with chemotherapy or allogeneic hematopoietic stem cell transplantation (allo-HSCT). 85 AML patients with AK1 expression report who received chemotherapy-alone and 71 who underwent allo-HSCT from The Cancer Genome Atlas database were identified and grouped into either AK1high or AK1low based on their AK1 expression level relative to the median. Then, overall survival (OS) and event-free survival (EFS) were compared between patients with high vs. low AK1 expression. In the chemotherapy group, high AK1 expression was favorable for both EFS (P=0.016) and OS (P=0.014). In the allo-HSCT group, there was no association for AK1 expression levels and clinical outcomes. Further analyses suggested that in the high AK1 expression group, EFS and OS were longer in patients treated with allo-HSCT compared with those treated with chemotherapy (P=0.0011; P<0.0001, respectively), whereas no significant differences were observed in the low AK1 expression group. In summary, we reported AK1 as an independent unfavorable prognostic factor of AML patients undergoing chemotherapy, and its use could also facilitate clinical decision-making in selecting treatment for AML patients. Patients with high AK1 expression may be recommended for early allo-HSCT.
本研究旨在探讨腺苷酸激酶 1(AK1)的表达水平是否与接受化疗或异基因造血干细胞移植(allo-HSCT)治疗的急性髓系白血病(AML)患者的预后相关。从癌症基因组图谱数据库中确定了 85 例接受单纯化疗且 AK1 表达报告的 AML 患者和 71 例接受 allo-HSCT 的患者,并根据 AK1 表达水平相对于中位数将其分为 AK1high 或 AK1low 组。然后,比较高 AK1 表达组与低 AK1 表达组之间的总生存期(OS)和无事件生存期(EFS)。在化疗组中,高 AK1 表达对 EFS(P=0.016)和 OS(P=0.014)均有利。在 allo-HSCT 组中,AK1 表达水平与临床结局之间没有关联。进一步分析表明,在高 AK1 表达组中,与接受化疗的患者相比,接受 allo-HSCT 的患者的 EFS 和 OS 更长(P=0.0011;P<0.0001),而在低 AK1 表达组中未观察到显著差异。总之,我们报告 AK1 是接受化疗的 AML 患者的独立不良预后因素,其使用也可以为 AML 患者的治疗选择提供临床决策。高 AK1 表达的患者可能被推荐进行早期 allo-HSCT。