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[预防异基因移植后急性白血病和骨髓增生异常综合征的复发:预防性和抢先性策略(SFGM-TC)]

[Preventing relapse of acute leukemias and myelodysplastic syndromes in post-allograft transplantation: Prophylactic and preemptive strategies (SFGM-TC)].

作者信息

Coiteux Valérie, Abellan Isabelle, Ahmad Imran, Boisnard Anne, Busquet Clémence, Ceballos Patrice, Coman Tereza, Godin Sandrine, Hermet Éric, Marcais Ambroise, Mamez Anne-Claire, Quessar Asmaa, Souchet Laetitia, Magro Léonardo, Simon Nicolas

机构信息

CHU de Lille, service des maladies du sang, unité de greffe de moelle osseuse et thérapie cellulaire, Lille, France.

CHU de Montpellier, service d'onco-hématologie pédiatrique, Montpellier, France.

出版信息

Bull Cancer. 2025 Jan;112(1S):S111-S124. doi: 10.1016/j.bulcan.2024.06.015. Epub 2024 Sep 5.

DOI:10.1016/j.bulcan.2024.06.015
PMID:39242256
Abstract

Disease relapse remains the first cause of mortality of hematological malignancies after allogeneic hematopoietic stem cell transplantation (allo-HCT) for acute myeloid and lymphoid leukemia (AML and ALL) and for myelodysplastic syndroms (MDS). More and more patients are eligible for allo-HCT over the years and for many of them, only reduced intensity conditioning is possible, which is associated with a higher risk of relapse. Knowledge and biotechnology allow us to better identify diseases at very high risk of relapse and to measure residual disease before allo-HCT. Planning post-transplant maintenance treatment as part of a prophylaxis strategy is now feasible. Monitoring biomarkers of residual disease and post-transplant chimerism after allo-HCT allows a preemptive strategy. Within the frame of the 14th annual workshops of the Francophone Society for Bone Marrow Transplantation and Cell Therapy, the working group reviewed the literature and discussed novel strategies and therapies used to prevent relapse post-allo-HCT. Innovative drugs have been developed recently. Their toxicity profile allows their use post-allo-HCT, albeit with precaution. We reviewed the use of FLT3 inhibitors for AML, BCR::ABL inhibitors for Philadelphia chromosome for ALL, hypomethylating agents and Bcl-2 inhibitors for AML and MDS. The indications of immunomodulation and infusion of donor lymphocytes have been reviewed. Finally, we outlined methods of follow-up and support for patients receiving these prophylactic treatments.

摘要

疾病复发仍然是急性髓系白血病和淋巴细胞白血病(AML和ALL)以及骨髓增生异常综合征(MDS)接受异基因造血干细胞移植(allo-HCT)后血液系统恶性肿瘤患者死亡的首要原因。多年来,越来越多的患者符合allo-HCT的条件,而且对其中许多人来说,只能进行减低强度预处理,这与较高的复发风险相关。知识和生物技术使我们能够更好地识别复发风险极高的疾病,并在allo-HCT前检测残留疾病。现在将移植后维持治疗作为预防策略的一部分进行规划是可行的。监测allo-HCT后的残留疾病生物标志物和移植后嵌合状态可采取先发制人的策略。在法语国家骨髓移植和细胞治疗协会第14届年度研讨会的框架内,工作组回顾了文献,并讨论了用于预防allo-HCT后复发的新策略和疗法。最近开发了一些创新药物。尽管要谨慎使用,但它们的毒性特征使其可在allo-HCT后使用。我们回顾了FLT3抑制剂用于AML、BCR::ABL抑制剂用于ALL的费城染色体、低甲基化剂以及Bcl-2抑制剂用于AML和MDS的情况。免疫调节和输注供体淋巴细胞的适应证也已得到回顾。最后,我们概述了接受这些预防性治疗患者的随访和支持方法。

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