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异基因造血干细胞移植后的去甲基化药物

Hypomethylating agents after allogeneic blood stem cell transplantation.

作者信息

Schroeder Thomas, Rautenberg Christina, Haas Rainer, Kobbe Guido

机构信息

Department of Hematology, Oncology and Clinical Immunology, University of Duesseldorf, Medical Faculty, Duesseldorf, Germany.

出版信息

Stem Cell Investig. 2016 Nov 28;3:84. doi: 10.21037/sci.2016.11.04. eCollection 2016.

Abstract

Allogeneic blood stem cell transplantation (allo-SCT) is a potentially curative treatment for patients with myeloid malignancies such as acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), but relapse remains the major cause of treatment failure. So far, therapeutic options for patients with AML or MDS who relapse after allo-SCT generally consisted of palliative care, low-dose or intensive chemotherapy as well as cellular therapies such as donor lymphocyte infusions (DLI) and second transplantation in selected cases. Nevertheless, the prognosis of patients with myeloid malignancies relapsing after allo-SCT remains dismal therefore asking for novel treatment strategies. Considering their well-balanced profile of good efficacy and moderate toxicity in the non-transplant setting, the hypomethylating agents (HMA) azacitidine (Aza) and decitabine (DAC) have also been tested either alone or in combination with DLI in the post-transplant period. This review summarizes the current knowledge about the use of these two HMA as pre-emptive, salvage or consolidation therapy mostly retrieved from retrospective studies but also from a few prospective trials. Within this review, we also comment on some practical issues such as optimal dose and schedule, the choice of HMA candidates and the role of additional cellular interventions. Finally, we also give an overview on the assumed mode of actions, ongoing research, clinical studies and potential combination partners aiming to improve this treatment approach.

摘要

异基因造血干细胞移植(allo-SCT)是治疗急性髓系白血病(AML)和骨髓增生异常综合征(MDS)等髓系恶性肿瘤患者的一种潜在治愈性疗法,但复发仍然是治疗失败的主要原因。到目前为止,allo-SCT后复发的AML或MDS患者的治疗选择通常包括姑息治疗、低剂量或强化化疗以及细胞疗法,如供体淋巴细胞输注(DLI),在特定情况下还包括二次移植。然而,allo-SCT后复发的髓系恶性肿瘤患者的预后仍然很差,因此需要新的治疗策略。考虑到它们在非移植环境中疗效良好且毒性适中的平衡特性,去甲基化药物(HMA)阿扎胞苷(Aza)和地西他滨(DAC)也已在移植后单独或与DLI联合进行了测试。本综述总结了目前关于这两种HMA作为抢先、挽救或巩固治疗的应用知识,这些知识大多来自回顾性研究,但也有一些前瞻性试验。在本综述中,我们还对一些实际问题进行了评论,如最佳剂量和给药方案、HMA候选药物的选择以及额外细胞干预的作用。最后,我们还概述了假定的作用方式、正在进行的研究、临床研究以及旨在改进这种治疗方法的潜在联合治疗伙伴。

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Hypomethylating agents after allogeneic blood stem cell transplantation.异基因造血干细胞移植后的去甲基化药物
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