Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, 610 University Ave, OPG Rm 6-222, Toronto, ON, Canada.
Department of Medicine, University of Toronto, Toronto, ON, M5G 2M9, Canada.
Int J Hematol. 2023 Jul;118(1):1-17. doi: 10.1007/s12185-023-03614-x. Epub 2023 May 22.
Allogeneic hematopoietic stem cell transplant (HCT) has improved survival for patients with acute myeloid leukemia (AML), especially for those at high risk of relapse. However, relapse remains the leading cause of treatment failure post-HCT, occurring in around 35-45% of patients, and leading to dismal outcomes. Strategies to reduce relapse risk are urgently needed, especially in the early post-transplant period before activation of the graft-versus-leukemia (GVL) effect. Maintenance therapy is a course of treatment given post-HCT with the expectation of reducing relapse risk. While there are currently no therapies approved for maintenance therapy for AML after HCT, there are a number of studies and ongoing investigations examining the role of maintenance therapies that include targeted agents against FLT3-ITD, BCL2, or IDH mutations, hypomethylating agents, immunomodulatory therapies and cellular therapies. In this review, we discuss the mechanistic and clinical data for post-transplant maintenance therapies in AML and strategies for maintenance therapy for AML after HCT.
异基因造血干细胞移植(HCT)提高了急性髓系白血病(AML)患者的生存率,特别是对于那些有高复发风险的患者。然而,移植后复发仍然是导致治疗失败的主要原因,约有 35-45%的患者会发生复发,并导致预后不良。因此迫切需要降低复发风险的策略,特别是在移植物抗白血病(GVL)效应激活之前的移植后早期阶段。维持治疗是在 HCT 后给予的治疗方案,期望降低复发风险。尽管目前尚无 AML 患者 HCT 后维持治疗的批准疗法,但有许多研究和正在进行的研究正在探讨维持治疗的作用,包括针对 FLT3-ITD、BCL2 或 IDH 突变、低甲基化剂、免疫调节疗法和细胞疗法的靶向药物。在这篇综述中,我们讨论了 AML 移植后维持治疗的机制和临床数据,以及 AML 患者 HCT 后维持治疗的策略。