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在 AML 患者中,应如何以及何时在表观遗传学治疗与化疗之间做出决策。

How and when to decide between epigenetic therapy and chemotherapy in patients with AML.

机构信息

Hôpital Saint-Louis, Institut Universitaire d'Hématologie, Université Paris Diderot, Paris, France.

出版信息

Hematology Am Soc Hematol Educ Program. 2017 Dec 8;2017(1):45-53. doi: 10.1182/asheducation-2017.1.45.

Abstract

Remission induction with chemotherapy has long been the frontline treatment of acute myeloid leukemia (AML). However, intensive therapy is limited in frail patients by its associated toxicity and higher rates of failure or relapse in patients with chemoresistant disease, such as secondary AML or poor-risk cytogenetics. Frailty and chemoresistance are more frequent in older adults with AML. In recent years, epigenetic therapies with the hypomethylating agents decitabine and azacitidine have been thoroughly explored in AML. The results of two pivotal studies carried out with these agents in older adults with newly diagnosed AML have challenged the role of intensive chemotherapy as the frontline treatment option in this high-risk population. Here, we review the results of treatment with intensive chemotherapy and hypomethylating agents in older patients with AML; discuss the patient- and disease-specific criteria to integrate into treatment decision making; and also, highlight the methodological limitations of cross-study comparison in this population.

摘要

化疗诱导缓解一直是急性髓系白血病(AML)的一线治疗方法。然而,强化治疗因其相关毒性以及在耐药疾病(如继发性 AML 或不良细胞遗传学)患者中失败或复发的更高比率,在体弱患者中受到限制。AML 老年患者中虚弱和耐药更为常见。近年来,去甲基化药物地西他滨和阿扎胞苷的表观遗传学治疗在 AML 中得到了深入探索。这两种药物在新诊断为 AML 的老年患者中进行的两项关键研究的结果挑战了强化化疗作为该高危人群一线治疗选择的作用。在这里,我们回顾了强化化疗和去甲基化药物在 AML 老年患者中的治疗结果;讨论了将整合到治疗决策中的患者和疾病特异性标准;并强调了该人群中跨研究比较的方法学局限性。

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