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造血干细胞移植后急性髓系白血病复发的防治:现状与未来展望

Prevention and Treatment of Acute Myeloid Leukemia Relapse after Hematopoietic Stem Cell Transplantation: The State of the Art and Future Perspectives.

作者信息

Leotta Salvatore, Condorelli Annalisa, Sciortino Roberta, Milone Giulio Antonio, Bellofiore Claudia, Garibaldi Bruno, Schininà Giovanni, Spadaro Andrea, Cupri Alessandra, Milone Giuseppe

机构信息

Division of Hematology, AOU "Policlinico G. Rodolico-San Marco", Via Santa Sofia 78, 95124 Catania, Italy.

出版信息

J Clin Med. 2022 Jan 4;11(1):253. doi: 10.3390/jcm11010253.

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) for high-risk acute myeloid leukemia (AML) represents the only curative option. Progress has been made in the last two decades in the pre-transplant induction therapies, supportive care, selection of donors and conditioning regimens that allowed to extend the HSCT to a larger number of patients, including those aged over 65 years and/or lacking an HLA-identical donor. Furthermore, improvements in the prophylaxis of the graft-versus-host disease and of infection have dramatically reduced transplant-related mortality. The relapse of AML remains the major reason for transplant failure affecting almost 40-50% of the patients. From 10 to 15 years ago to date, treatment options for AML relapsing after HSCT were limited to conventional cytotoxic chemotherapy and donor leukocyte infusions (DLI). Nowadays, novel agents and targeted therapies have enriched the therapeutic landscape. Moreover, very recently, the therapeutic landscape has been enriched by manipulated cellular products (CAR-T, CAR-CIK, CAR-NK). In light of these new perspectives, careful monitoring of minimal-residual disease (MRD) and prompt application of pre-emptive strategies in the post-transplant setting have become imperative. Herein, we review the current state of the art on monitoring, prevention and treatment of relapse of AML after HSCT with particular attention on novel agents and future directions.

摘要

异基因造血干细胞移植(HSCT)是高危急性髓系白血病(AML)唯一的治愈选择。在过去二十年中,移植前诱导治疗、支持治疗、供体选择和预处理方案取得了进展,这使得HSCT能够应用于更多患者,包括65岁以上和/或缺乏HLA相合同胞供体的患者。此外,移植物抗宿主病和感染预防措施的改进显著降低了移植相关死亡率。AML复发仍然是移植失败的主要原因,影响了近40%-50%的患者。从10到15年前至今,HSCT后复发AML的治疗选择仅限于传统细胞毒性化疗和供体白细胞输注(DLI)。如今,新型药物和靶向治疗丰富了治疗手段。此外,最近,经改造的细胞产物(CAR-T、CAR-CIK、CAR-NK)也丰富了治疗手段。鉴于这些新观点,在移植后环境中仔细监测微小残留病(MRD)并及时应用抢先治疗策略变得势在必行。在此,我们综述了HSCT后AML复发监测、预防和治疗的当前技术水平,特别关注新型药物和未来方向。

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