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异基因造血细胞移植后的药物维持治疗

Pharmacological Maintenance Therapies After Allogeneic Hematopoietic Cell Transplantation.

作者信息

Walia Ritika, Chen Yi-Bin

机构信息

University of Massachusetts, Worcester, MA, USA.

Massachusetts General Hospital, Boston, MA, USA.

出版信息

Adv Exp Med Biol. 2025;1475:193-207. doi: 10.1007/978-3-031-84988-6_11.

Abstract

Disease relapse is the leading cause of failure for patients with hematological malignancies who have received allogeneic hematopoietic cell transplantation (HCT). Maintenance therapy administered after HCT is a promising strategy to reduce the incidence of relapse and enhance the curative potential of HCT. Historically, maintenance therapy was not possible due to off-target toxicities from conventional chemotherapy. With the advent of specifically targeted agents-such as those targeting BCR-ABL, FLT3, IDH1, IDH2 and Menin-therapy given in the immediate period after HCT while patients remain in remission has become a reality. Research investigations and clinical applications of this approach have greatly increased in recent years, with a rapidly expanding number of available therapeutic agents waiting to be tested in the post-transplant setting. However, many questions and challenges remain regarding the feasibility and clinical impact of maintenance therapy after HCT. In this chapter, we review the published data as well as ongoing studies regarding the rapidly evolving field of maintenance therapy after HCT.

摘要

疾病复发是接受异基因造血细胞移植(HCT)的血液系统恶性肿瘤患者治疗失败的主要原因。HCT后给予维持治疗是一种很有前景的策略,可降低复发率并提高HCT的治愈潜力。从历史上看,由于传统化疗的脱靶毒性,维持治疗是不可能的。随着特异性靶向药物的出现,如那些靶向BCR-ABL、FLT3、IDH1、IDH2和Menin的药物,在患者仍处于缓解期时于HCT后立即进行治疗已成为现实。近年来,这种方法的研究调查和临床应用大幅增加,有越来越多的可用治疗药物等待在移植后环境中进行测试。然而,关于HCT后维持治疗的可行性和临床影响仍存在许多问题和挑战。在本章中,我们回顾了已发表的数据以及关于HCT后维持治疗这一快速发展领域的正在进行的研究。

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