Allogeneic stem cell transplantation for MDS-clinical issues, choosing preparative regimens and outcome.

IF 2.2 4区 医学 Q3 HEMATOLOGY Leukemia & Lymphoma Pub Date : 2025-08-01 Epub Date: 2025-03-12 DOI:10.1080/10428194.2025.2476652
Lara Bischof, Jule Ussmann, Uwe Platzbecker, Madlen Jentzsch, Georg-Nikolaus Franke
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Abstract

Despite the vast heterogeneity of myelodysplastic neoplasm (MDS), treatment options are limited and an allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the only curative approach. While, subsequently, allo-HSCT is the treatment of choice in fit high-risk MDS patients younger than 70 years, it should only be considered in young and fit low-risk MDS patients who suffer from severe and life threatening cytopenias, and fail all available conservative treatment options. With the increasing use of mismatched or haploidentical donors, the majority of MDS patients will have a suitable donor available, however, matched donors should still be preferred if rapidly available. Strategies to prevent relapse after allo-HSCT are scarce, and include the use of donor lymphocytes or the experimental use of hypomethylating agents in patients with impeding relapse detected by MRD or chimerism evaluation. Here, we summarize current treatment options and factors to consider in the context of allo-HSCT in MDS.

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异体干细胞移植用于mds的临床问题,选择准备方案和结果。
尽管骨髓增生异常肿瘤(MDS)具有巨大的异质性,但治疗选择有限,同种异体造血干细胞移植(alloo - hsct)仍然是唯一的治疗方法。然而,同种异体造血干细胞移植是适合70岁以下高危MDS患者的治疗选择,只有年轻健康的低风险MDS患者患有严重和危及生命的细胞减少症,并且所有可用的保守治疗方案都失败时才应该考虑。随着错配或单倍体相同供体的使用越来越多,大多数MDS患者将有一个合适的供体,然而,匹配供体仍应优先考虑,如果快速找到。预防同种异体造血干细胞移植后复发的策略很少,包括在MRD或嵌合评价检测到阻碍复发的患者中使用供体淋巴细胞或实验性地使用低甲基化药物。在这里,我们总结了目前在MDS中进行同种异体造血干细胞移植的治疗方案和需要考虑的因素。
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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