Division of Hematology and Oncology, University of Leipzig, Leipzig, Germany.
Onco Targets Ther. 2013 Jun 20;6:741-8. doi: 10.2147/OTT.S45459. Print 2013.
Epigenetic modulations, including changes in DNA cytosine methylation, are implicated in the pathogenesis and progression of acute myeloid leukemia (AML). Azacitidine is a hypomethylating agent that is incorporated into RNA as well as DNA. Thus, there is a rationale to its use in patients with AML. We determined whether baseline and/or early changes in the methylation of long interspersed element (LINE)-1 or CDH13 correlate with bone marrow blast clearance, hematological response, or survival in patients with AML treated with azacitidine.
An open label, phase I/II trial was performed in 40 AML patients (median bone marrow blast count was 42%) unfit for intensive chemotherapy treated with azacitidine 75 mg/m(2)/day subcutaneously for 5 days every 4 weeks. Bone marrow mononuclear cell samples were taken on day 0 (pretreatment) and day 15 during the first treatment cycle; LINE-1 and CDH13 methylation levels were quantified by methylation-specific, semiquantitative, real-time polymerase chain reaction.
Treatment with azacitidine significantly reduced LINE-1 but not CDH13 methylation levels over the first cycle (P < 0.0001). Absolute LINE-1 methylation levels tended to be lower on day 0 (P = 0.06) and day 15 of cycle 1 (P = 0.03) in patients who went on to achieve subsequent complete remission, partial remission or hematological improvement versus patients with stable disease. However, the decrease in LINE-1 methylation over the first treatment cycle did not correlate with subsequent response (P = 0.31). Baseline methylation levels of LINE-1 or CDH13 did not correlate with disease-related prognostic factors, including cytogenetic risk, relapsed/refractory AML, or presence of NPM1 or FLT3 mutations. No correlation was observed between LINE-1 or CDH13 methylation levels and overall survival.
Analysis of baseline LINE-1 methylation levels may help identify elderly AML patients who are most likely to respond to azacitidine therapy.
表观遗传修饰,包括 DNA 胞嘧啶甲基化的改变,与急性髓系白血病(AML)的发病机制和进展有关。阿扎胞苷是一种低甲基化剂,可整合到 RNA 和 DNA 中。因此,它在 AML 患者中有其应用的理由。我们确定在接受阿扎胞苷治疗的 AML 患者中,基线和/或 LINE-1 或 CDH13 甲基化的早期变化是否与骨髓原始细胞清除、血液学反应或生存相关。
对 40 名不适合强化化疗的 AML 患者(中位骨髓原始细胞计数为 42%)进行了一项开放标签的 I/II 期临床试验,这些患者接受阿扎胞苷 75 mg/m2/天皮下注射,每 4 周 5 天。在第一个治疗周期的第 0 天(预处理)和第 15 天采集骨髓单核细胞样本;通过甲基化特异性、半定量、实时聚合酶链反应定量测定 LINE-1 和 CDH13 甲基化水平。
阿扎胞苷治疗在第一个周期中显著降低了 LINE-1 但未降低 CDH13 的甲基化水平(P < 0.0001)。在随后获得完全缓解、部分缓解或血液学改善的患者中,第 0 天(P = 0.06)和第 1 个周期的第 15 天(P = 0.03)的绝对 LINE-1 甲基化水平倾向于较低,而在疾病稳定的患者中则较低。然而,第一个治疗周期中 LINE-1 甲基化的降低与随后的反应无关(P = 0.31)。LINE-1 或 CDH13 的基线甲基化水平与疾病相关的预后因素,包括细胞遗传学风险、复发/难治性 AML 或存在 NPM1 或 FLT3 突变,均无相关性。未观察到 LINE-1 或 CDH13 甲基化水平与总生存期之间存在相关性。
分析基线 LINE-1 甲基化水平可能有助于识别最有可能对阿扎胞苷治疗有反应的老年 AML 患者。