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单倍体相合干细胞移植治疗急性髓系白血病:当前疗法、挑战与未来展望

Haploidentical Stem Cell Transplantation for Acute Myeloid Leukemia: Current Therapies, Challenges and Future Prospective.

作者信息

Chang Ying-Jun, Zhao Xiang-Yu, Huang Xiao-Jun

机构信息

Peking University Institute of Hematology, Peking University People's Hospital, Beijing, China.

National Clinical Research Center for Hematologic Disease, Beijing, China.

出版信息

Front Oncol. 2021 Oct 28;11:758512. doi: 10.3389/fonc.2021.758512. eCollection 2021.

Abstract

Haploidentical stem cell transplantation (haplo-SCT), an alternative donor source, offers a curative therapy for patients with acute myeloid leukemia (AML) who are transplant candidates. Advances in transplantation techniques, such as donor selection, conditioning regimen modification, and graft-versus-host disease prophylaxis, have successfully improved the outcomes of AML patients receiving haplo-SCT and extended the haploidentical transplant indictions for AML. Presently, treating AML, secondary AML, therapy-related AML and refractory and relapsed AML with haplo-SCT can achieve comparable outcomes to those of human leukocyte antigen (HLA)-matched sibling donor transplantation (MSDT), unrelated donor transplantation or umbilical cord blood transplantation. For some subgroups of AML subjects, such as patients with positive pretransplantation minimal/measurable residual disease, recent studies suggest that haplo-SCT might be superior to MSDT in decreasing relapse and improving survival. Unfortunately, for patients with AML after haplo-SCT, relapse and infections remain the causes of death that restrict further improvement in clinical outcomes. In this review, we discuss the recent advances and challenges in haplo-SCT for AML treatment, mainly focusing on unmanipulated haplo-SCT protocols. We provide an outlook on future prospects and suggest that relapse prophylaxis, intervention, and treatment, as well as infection prevention and therapy, are areas of active research in AML patients who receive haploidentical allografts.

摘要

单倍体相合干细胞移植(haplo-SCT)作为一种供体来源选择,为符合移植条件的急性髓系白血病(AML)患者提供了一种治愈性疗法。移植技术的进步,如供体选择、预处理方案调整和移植物抗宿主病预防等,已成功改善了接受haplo-SCT的AML患者的治疗效果,并扩大了AML的单倍体相合移植适应症。目前,采用haplo-SCT治疗AML、继发性AML、治疗相关AML以及难治性和复发性AML,可取得与人类白细胞抗原(HLA)相合的同胞供体移植(MSDT)、无关供体移植或脐带血移植相当的治疗效果。对于AML受试者的某些亚组,如移植前微小/可测量残留病呈阳性的患者,最近的研究表明,haplo-SCT在降低复发率和提高生存率方面可能优于MSDT。不幸的是,对于接受haplo-SCT后的AML患者,复发和感染仍然是导致死亡的原因,限制了临床疗效的进一步提高。在本综述中,我们讨论了haplo-SCT治疗AML的最新进展和挑战,主要聚焦于未处理的haplo-SCT方案。我们展望了未来前景,并指出预防复发、干预和治疗以及预防和治疗感染是接受单倍体相合同种异体移植的AML患者积极研究的领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60a0/8581046/9b76ef051d6e/fonc-11-758512-g001.jpg

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