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治疗前长散在核元件(LINE)-1 甲基化水平,而非治疗下的早期低甲基化,可预测老年急性髓系白血病患者对阿扎胞苷的血液学反应。

Pretreatment long interspersed element (LINE)-1 methylation levels, not early hypomethylation under treatment, predict hematological response to azacitidine in elderly patients with acute myeloid leukemia.

机构信息

Division of Hematology and Oncology, University of Leipzig, Leipzig, Germany.

出版信息

Onco Targets Ther. 2013 Jun 20;6:741-8. doi: 10.2147/OTT.S45459. Print 2013.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

Analysis of baseline LINE-1 methylation levels may help identify elderly AML patients who are most likely to respond to azacitidine therapy.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c39e/3699298/3d0b381cf549/ott-6-741Fig1.jpg

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