[预防移植后急性白血病和骨髓增生异常综合征复发:预防性和先发制人的策略(SFGM-TC)]。

Bulletin du cancer Pub Date : 2025-01-01 Epub Date: 2024-09-05 DOI:10.1016/j.bulcan.2024.06.015
Valérie Coiteux, Isabelle Abellan, Imran Ahmad, Anne Boisnard, Clémence Busquet, Patrice Ceballos, Tereza Coman, Sandrine Godin, Éric Hermet, Ambroise Marcais, Anne-Claire Mamez, Asmaa Quessar, Laetitia Souchet, Léonardo Magro, Nicolas Simon
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引用次数: 0

摘要

异基因造血干细胞移植(allo-HCT)治疗急性髓性和淋巴性白血病(AML和ALL)以及骨髓增生异常综合征(MDS)后,疾病复发仍是血液恶性肿瘤死亡的首要原因。多年来,越来越多的患者符合allo-HCT的条件,但对其中许多人来说,只能进行强度降低的调理,而这与较高的复发风险有关。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,并在同种异体血细胞移植前测量残留疾病。作为预防策略的一部分,计划移植后的维持治疗现在是可行的。在同种异体肝移植后监测残留疾病的生物标志物和移植后嵌合体,可以采取先发制人的策略。在第14届法语骨髓移植和细胞治疗协会年度研讨会上,工作组回顾了相关文献,并讨论了用于预防异体血细胞移植后复发的新策略和疗法。最近开发出了创新药物。这些药物的毒性特征允许在allo-HCT术后使用,但需谨慎。我们回顾了治疗急性髓细胞性白血病的FLT3抑制剂、治疗费城染色体性白血病的BCR::ABL抑制剂、治疗急性髓细胞性白血病和MDS的低甲基化药物和Bcl-2抑制剂。我们还回顾了免疫调节和输注供体淋巴细胞的适应症。最后,我们概述了接受这些预防性治疗的患者的随访和支持方法。
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[Preventing relapse of acute leukemias and myelodysplastic syndromes in post-allograft transplantation: Prophylactic and preemptive strategies (SFGM-TC)].

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.

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