Section of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL USA.
Division of Blood and Marrow Transplantation and Cellular Therapy, Stanford University, Stanford, CA, USA.
Haematologica. 2022 Dec 1;107(12):2783-2793. doi: 10.3324/haematol.2022.280638.
Measurable residual disease (MRD) is the most powerful independent predictor of risk of relapse and long-term survival in adults and children with acute lymphoblastic leukemia (ALL). For almost all patients with ALL there is a reliable method to evaluate MRD, which can be done using multi-color flow cytometry, quantitative polymerase chain reaction to detect specific fusion transcripts or immunoglobulin/T-cell receptor gene rearrangements, and high-throughput next-generation sequencing. While next-generation sequencing-based MRD detection has been increasingly utilized in clinical practice due to its high sensitivity, the clinical significance of very low MRD levels (<10-4) is not fully characterized. Several new immunotherapy approaches including blinatumomab, inotuzumab ozogamicin, and chimeric antigen receptor T-cell therapies have demonstrated efficacy in eradicating MRD in patients with B-ALL. However, new approaches to target MRD in patients with T-ALL remain an unmet need. As our MRD detection assays become more sensitive and expanding novel therapeutics enter clinical development, the future of ALL therapy will increasingly utilize MRD as a criterion to either intensify or modify therapy to prevent relapse or de-escalate therapy to reduce treatment-related morbidity and mortality.
残留疾病(MRD)是急性淋巴细胞白血病(ALL)成人和儿童复发风险和长期生存的最有力的独立预测因素。对于几乎所有 ALL 患者,都有一种可靠的方法来评估 MRD,可以使用多色流式细胞术、定量聚合酶链反应检测特定融合转录本或免疫球蛋白/T 细胞受体基因重排,以及高通量下一代测序。虽然基于下一代测序的 MRD 检测由于其高灵敏度而在临床实践中越来越多地被应用,但非常低的 MRD 水平(<10-4)的临床意义尚未完全确定。几种新的免疫疗法,包括blinatumomab、inotuzumab ozogamicin 和嵌合抗原受体 T 细胞疗法,已证明在消除 B-ALL 患者的 MRD 方面有效。然而,针对 T-ALL 患者的 MRD 的新方法仍然是一个未满足的需求。随着我们的 MRD 检测方法变得更加敏感,并且新的治疗方法进入临床开发,ALL 治疗的未来将越来越多地将 MRD 作为标准,要么加强治疗,要么改变治疗方案,以防止复发,要么降低治疗相关的发病率和死亡率。