Do hypomethylating agents prevent relapse after Allo-HCT?

Thomas Schroeder, Christina Rautenberg, Rainer Haas, Ulrich Germing, Guido Kobbe
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引用次数: 1

Abstract

Relapse is the main cause of treatment failure in patients with acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) and limits the curative potential of allogeneic blood stem cell transplantation (allo-HCT). Many patients can either not tolerate or do not achieve durable remissions through commonly used treatment options such as salvage chemotherapy, donor lymphocyte infusions (DLI), and/or second transplants. Thus, patients who relapse after allo-HCT have a very poor prognosis with the currently available therapies implicating the great medical need for relapse prevention. After having demonstrated efficacy and tolerability as salvage therapy in patients with myeloid malignancies who relapse after allo-HCT the hypomethylating agents azacitidine (Aza) and decitabine (DAC) have also been tested as prophylactic and preemptive approaches in patients with AML and MDS after allo-SCT. Here, we summarize the current literature reporting on results from prospective trials and retrospective analyses regarding the prophylactic and preemptive use of Aza and DAC after allo-SCT and aim to give an answer if these hypomethylating agents (HMA) are able to prevent relapse of myeloid malignancies after allo-HCT.

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低甲基化药物能防止Allo-HCT后复发吗?
复发是急性髓细胞白血病(AML)和骨髓增生异常综合征(MDS)患者治疗失败的主要原因,并限制了异基因造血干细胞移植(allo-HCT)的治疗潜力。通过常用的治疗方案,如挽救性化疗、供体淋巴细胞输注(DLI)和/或第二次移植,许多患者要么无法耐受,要么无法实现持久的缓解。因此,allo-HCT后复发的患者预后非常差,目前可用的治疗方法意味着预防复发的巨大医学需求。在异基因造血干细胞移植后复发的髓系恶性肿瘤患者中,低甲基化药物阿扎胞苷(Aza)和地西他滨(DAC)已被证明是补救治疗的有效性和耐受性后,还被测试为异基因造血细胞移植后AML和MDS患者的预防性和先发制人的方法。在此,我们总结了目前关于异基因造血干细胞移植后预防性和优先使用Aza和DAC的前瞻性试验和回顾性分析结果的文献报道,并旨在给出这些低甲基化药物(HMA)是否能够预防异基因造血细胞移植后髓系恶性肿瘤复发的答案。
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