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阿扎胞苷联合来那度胺治疗骨髓增生异常综合征或急性髓系白血病——明智的联合?

Combination of azacitidine and lenalidomide in myelodysplastic syndromes or acute myeloid leukemia-a wise liaison?

机构信息

Technical University, Dresden, Germany.

出版信息

Leukemia. 2013 Sep;27(9):1813-9. doi: 10.1038/leu.2013.140. Epub 2013 May 6.

Abstract

Treatment options for older patients with advanced myelodysplastic syndromes (MDS) or acute myeloid leukemia (AML) are limited and the prognosis remains poor, thereby warranting development of novel therapies. Aberrant epigenetic modifications, including altered DNA methylation, seem to contribute to the pathogenesis of these patients. In fact, hypomethylating agents (HMA) like azacitidine have been successfully used in clinical trials and achieved approval from health authorities. There is now growing evidence suggesting that the combination of drugs with different mechanisms of action might offer a potential benefit to these patients. This is especially done with the intention to synergize the positive effects of each drug on the defective hematopoiesis while sparing potential side effects and toxicities. Combination of HMA with histone deacetylase inhibitors, although mechanistically very tempting, have not yielded convincing improvement of the results in the majority of trials compared to single agent HMA treatment. Currently, combination therapies of azacitidine with lenalidomide appear to be promising thus making them an appealing option for treatment in these patients.

摘要

治疗老年骨髓增生异常综合征(MDS)或急性髓系白血病(AML)患者的方法有限,预后仍然较差,因此需要开发新的治疗方法。异常的表观遗传修饰,包括改变的 DNA 甲基化,似乎有助于这些患者的发病机制。事实上,低甲基化剂(HMA)如阿扎胞苷已在临床试验中成功应用,并获得了卫生部门的批准。越来越多的证据表明,具有不同作用机制的药物联合使用可能会给这些患者带来潜在的益处。这主要是为了协同每种药物对缺陷性造血的积极作用,同时避免潜在的副作用和毒性。HMA 与组蛋白去乙酰化酶抑制剂的联合应用,尽管在机制上非常有吸引力,但与单独使用 HMA 治疗相比,在大多数试验中并没有产生令人信服的结果改善。目前,阿扎胞苷与来那度胺的联合治疗似乎很有前途,因此成为这些患者治疗的一个有吸引力的选择。

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