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首页> 外文期刊>Annals of hematology >Efficacy of the hypomethylating agents as frontline, salvage, or consolidation therapy in adults with acute myeloid leukemia (AML)
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Efficacy of the hypomethylating agents as frontline, salvage, or consolidation therapy in adults with acute myeloid leukemia (AML)

机译:次甲基化剂在成人急性髓细胞白血病(AML)中作为一线治疗,抢救或巩固治疗的功效

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摘要

The hypomethylating agents (HAs), azacitidine and decitabine, have emerged as an alternative to initial and salvage therapy in patients with acute myeloid leukemia (AML). Little is known about how AML responds to hypomethylating agents after standard therapy, and the activity of these agents in a real-world setting is not well studied. We retrospectively examined data for 75 consecutive AML patients at Wake Forest from 2002 to 2011 treated with HAs either as first-line (n = 34), salvage (n = 28), or consolidation (n = 13) therapy. We collected data on age, gender, race, Charlson comorbidity index (CCI), cytogenetics, type of treatment, complete remission (CR), complete remission with incomplete count recovery (CRi), and survival. Statistical analysis was performed using Kaplan-Meier estimates and Cox proportional hazards models. Frontline response rate (CR + CRi) was 26.5 %, and median overall survival (OS) was 3.4 months (95 % CI 1.3-7.4), with 18 % alive at 1 year. In the salvage cohort, the response rate was significantly lower compared to frontline (3.6 versus 26.5 %, p = 0.017). Despite the reduced response, OS from time of HA treatment was longer than frontline at 8.2 months (CI 4.8-10.3). In the consolidation cohort, OS was 13.8 months (CI 8.0-21.6) with one patient in remission more than 30 months from diagnosis. These data suggest that prior cytotoxic therapy decreases marrow response rates to HAs but not survival. Furthermore, use of hypomethylating agents for consolidation resulted in a median overall survival over 1 year in a cohort of older patients. This suggests that hypomethylating agents have activity in all phases of AML treatment.
机译:次甲基化剂(HAs),阿扎胞苷和地西他滨已成为急性髓细胞性白血病(AML)患者初始和挽救疗法的替代方法。关于标准疗法后AML对低甲基化药物的反应知之甚少,而且在现实环境中这些药物的活性还没有得到很好的研究。我们回顾性研究了2002年至2011年Wake Forest连续75例AML患者的数据,这些患者接受过HA作为一线治疗(n = 34),打捞(n = 28)或巩固(n = 13)治疗。我们收集了有关年龄,性别,种族,查尔森合并症(CCI),细胞遗传学,治疗类型,完全缓解(CR),完全缓解及不完全计数恢复(CRi)和生存率的数据。使用Kaplan-Meier估计和Cox比例风险模型进行统计分析。一线反应率(CR + CRi)为26.5%,中位总体生存期(OS)为3.4个月(95%CI为1.3-7.4),其中1%存活1%。在救助队列中,响应率明显低于第一线(3.6对26.5%,p = 0.017)。尽管反应降低,但从HA治疗开始的OS在8.2个月时仍比一线要长(CI 4.8-10.3)。在合并队列中,OS为13.8个月(CI 8.0-21.6),其中一名患者在诊断后超过30个月缓解。这些数据表明,先前的细胞毒性治疗会降低骨髓对HA的反应率,但不会降低生存率。此外,使用次甲基化剂进行巩固治疗可导致一组老年患者的中位总生存期超过1年。这表明低甲基化剂在AML治疗的所有阶段均具有活性。

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