异基因造血干细胞移植治疗急性白血病的进展。

Yasuhito Nannya, Auro Viswabandya, Peihua Lu
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摘要

在急性白血病方面,以异体造血干细胞移植(allo-SCT)为中心的治疗策略取得了进展,本文介绍了其中的三种。对于首次完全缓解(CR1)的急性髓性白血病(AML),异体干细胞移植的适应症一直存在争议。基因组医学帮助我们更深入地了解了这种疾病,其中一些可能成为预后因素。这些基因异常还有助于测量最小残留病(MRD),并为估计化疗疗效提供更多线索。结合现有的预后因素,这些数据可用于构建更准确的预后模型,为 CR1 期急性髓细胞白血病患者提供异体 SCT 的最佳指征。此外,异体造血干细胞移植后高风险急性髓细胞白血病的整体治疗算法应包括预防性和先发制人的治疗,以防止复发。这包括使用供体淋巴细胞输注(DLI)的免疫疗法、FLT3突变急性髓细胞白血病的FLT3抑制剂、低甲基化药物或DLI与这些药物的组合。目前正在进行临床试验,以阐明这些策略的作用,从而为预防高风险急性髓细胞性白血病复发提供适应风险的治疗方法。CD19 靶向嵌合抗原受体(CAR)T 细胞疗法可诱导 B 型急性淋巴白血病(B-ALL)患者产生显著反应,但复发仍是一个主要问题。因此,建议儿童和成人患者在接受 CAR-T 细胞疗法治疗 B-ALL 后,接受异体 SCT 作为巩固治疗。通过CAR-T细胞疗法获得完全缓解(CR)被认为是一种很有希望的allo-SCT桥接疗法。目前正在开发新型 CAR-T 治疗技术,以改变其作为移植前治疗的角色。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advances in Allogeneic Hematopoietic Stem Cell Transplantation for Acute Leukemia.

In acute leukemia, advances have been made in therapeutic strategies centered on allogeneic hematopoietic stem cell transplantation (allo-SCT), three of which are presented here. The indication of allo-SCT for acute myeloid leukemia (AML) in 1st complete remission (CR1) has been debated. Genomic medicine has helped us gain a deeper understanding of this disease, some of which may serve as prognostic factors. Such genetic abnormalities could also help measure minimal residual disease (MRD) and provide additional clues to estimate the efficacy of chemotherapy. Combined with existing prognostic factors, these data can be used to construct a more accurate prognostic model, providing an optimal indication of allo-SCT for AML in CR1. Furthermore, overall treatment algorithms for high-risk AML after allo-SCT should include prophylactic and pre-emptive treatment to prevent relapse. These include immunotherapy using donor lymphocyte infusion (DLI), FLT3 inhibitors in FLT3-mutated AML, hypomethylating agents, or a combination of DLI with these agents. Clinical trials are currently ongoing to elucidate the role of these strategies, which will lead to a risk-adapted treatment for preventing relapse in high-risk AML. CD19-targeted chimeric antigen receptor (CAR) T-cell therapy induces a remarkable response in B-acute lymphoid leukemia (B-ALL); however, relapse remains a major problem. In this regard, allo-SCT as a consolidation treatment after CAR-T cell therapy for B-ALL is recommended for pediatric and adult patients. Achieving complete remission (CR) with CAR-T cell therapy is considered a promising bridging therapy to allo-SCT. Novel CAR-T treatment techniques are being developed to change their role as a pre-transplant treatment.

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