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首页> 外文期刊>Journal of Clinical Oncology >Therapeutic advances in acute myeloid leukemia.
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Therapeutic advances in acute myeloid leukemia.

机译:急性髓细胞白血病的治疗进展。

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The choice of treatment approach and outcome in acute myeloid leukemia (AML) depends on the age of the patient. In younger patients, arbitrarily defined as being younger than 60 years, 70% to 80% enter complete disease remission with several anthracycline-based chemotherapy combinations. Consolidation with high-dose cytarabine or stem-cell transplantation in high-risk patients will restrict overall relapse to approximately 50%. A number of demographic features can predict the outcome of treatment including cytogenetics and an increasing list of molecular features (ie, FLT3, NPM1, MLL, WT1, CEBPalpha, EVI1). These are increasingly being used to direct postinduction therapy, but they are also molecular targets for a new generation of small molecule inhibitors that are in early development; however, randomized data have yet to emerge. In older patients who comprise the majority, which will increase with demographic change, the initial clinical decision to be made is whether the patient should receive an intensive or nonintensive approach. If the same anthracycline/cytarabine-based approach is deployed, the remission rate will be around 50%, but the risk of subsequent relapse is approximately 85% at 3 years. This difference from younger patients is explained partly by the ability of patients to tolerate effective therapy, and also the aggregation of several poor risk factors compared with the young. There remains a substantial proportion of patients older than 60 years who do not receive intensive chemotherapy. Their survival is approximately 4 months, but there is considerable interest in developing new treatments for this patient group, including novel nucleoside analogs and several other agents.
机译:急性髓细胞性白血病(AML)的治疗方法和结果的选择取决于患者的年龄。在任意定义为60岁以下的年轻患者中,有70%至80%的患者通过几种以蒽环类为基础的化学疗法联合治疗可完全缓解疾病。高危患者合并大剂量阿糖胞苷或干细胞移植可将总体复发率限制在约50%。许多人口统计学特征可以预测治疗的结果,包括细胞遗传学和越来越多的分子特征(即FLT3,NPM1,MLL,WT1,CEBPalpha,EVI1)。这些被越来越多地用于指导诱导后治疗,但它们还是处于早期开发阶段的新一代小分子抑制剂的分子靶标。但是,随机数据尚未出现。在占多数的老年患者中,这将随着人口统计学的变化而增加,最初的临床决策是患者应该接受强化治疗还是非强化治疗。如果采用相同的基于蒽环/阿糖胞苷的方法,其缓解率将约为50%,但3年后复发的风险约为85%。与年轻患者的区别部分是由于患者耐受有效治疗的能力以及与年轻患者相比几种不良危险因素的聚集所致。 60岁以上的患者中仍有很大一部分未接受强化化疗。它们的生存期约为4个月,但是对于开发针对该患者组的新疗法(包括新型核苷类似物和几种其他药物)有相当大的兴趣。

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