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在骨髓增生异常综合征患者中,低甲基化药物是否正在取代异基因干细胞移植前的诱导型化疗?

Are hypomethylating agents replacing induction-type chemotherapy before allogeneic stem cell transplantation in patients with myelodysplastic syndrome?

作者信息

Yakoub-Agha Ibrahim, Deeg Joachim

机构信息

Bone Marrow Transplantation Unit, University-Hospital, Lille, France; INSERM U995, Lille, France.

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; University of Washington School of Medicine, Seattle, Washington.

出版信息

Biol Blood Marrow Transplant. 2014 Dec;20(12):1885-90. doi: 10.1016/j.bbmt.2014.06.023. Epub 2014 Jun 24.

Abstract

Cytoreductive treatment before allogeneic hematopoietic stem cell transplantation (allo-SCT) with the objective of reducing the incidence of disease relapse post-transplant in patients with myelodysplastic syndrome (MDS) is a matter of debate. The achievement of complete remission (CR) before allo-SCT improves post-transplantation outcome, although it is not clear whether this reflects the selection of patients with more responsive disease or is related to a reduction in disease burden. Higher CR rates in patients with MDS are obtained with induction chemotherapy (ICT) than with hypomethylating agents (HMAs), although HMAs may be active in patients with complex karyotypes in whom ICT almost invariably fails. Furthermore, HMAs have a good toxicity profile compared with ICT and may therefore be considered especially in older patients and in patients with comorbidities. However, all interventions aimed at reducing disease burden before allo-SCT expose patients to the risk of complications, which may prevent them from undergoing transplantation. Therefore, up-front allo-SCT is an option, particularly for patients with life-threatening cytopenias. In this review we discuss the main pretransplant therapeutic approaches and propose a decision-model based on clinical considerations. However, only prospective randomized trials can address the issue definitively.

摘要

对于骨髓增生异常综合征(MDS)患者,在异基因造血干细胞移植(allo-SCT)前进行减瘤治疗以降低移植后疾病复发率是一个存在争议的问题。allo-SCT前实现完全缓解(CR)可改善移植后的结局,尽管尚不清楚这是反映了选择了对疾病反应性更高的患者,还是与疾病负担的减轻有关。MDS患者接受诱导化疗(ICT)比接受去甲基化药物(HMA)能获得更高的CR率,尽管HMA可能对染色体核型复杂的患者有效,而ICT对这类患者几乎总是无效。此外,与ICT相比,HMA具有良好的毒性特征,因此尤其在老年患者和合并症患者中可能会被考虑使用。然而,所有旨在在allo-SCT前减轻疾病负担的干预措施都会使患者面临并发症风险,这可能会阻止他们接受移植。因此,早期allo-SCT是一种选择,特别是对于有危及生命的血细胞减少症的患者。在本综述中,我们讨论了主要的移植前治疗方法,并基于临床考虑提出了一个决策模型。然而,只有前瞻性随机试验才能明确解决这个问题。

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