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J Clin Oncol. 2024 Sep 10;42(26):3140-3150. doi: 10.1200/JCO.24.00108. Epub 2024 Jul 19.
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Leuk Lymphoma. 2024 Oct;65(10):1405-1417. doi: 10.1080/10428194.2024.2364043. Epub 2024 Jun 8.
5
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Leukemia. 2024 Jun;38(6):1315-1322. doi: 10.1038/s41375-024-02272-0. Epub 2024 May 14.
6
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成人急性淋巴细胞白血病中可测量残留病的临床应用:美国专家小组的建议

Clinical use of measurable residual disease in adult ALL: recommendations from a panel of US experts.

作者信息

Short Nicholas J, Aldoss Ibrahim, DeAngelo Daniel J, Konopleva Marina, Leonard Jessica, Logan Aaron C, Park Jae, Shah Bijal, Stock Wendy, Jabbour Elias

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.

Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.

出版信息

Blood Adv. 2025 Mar 25;9(6):1442-1451. doi: 10.1182/bloodadvances.2024015441.

DOI:10.1182/bloodadvances.2024015441
PMID:39853316
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11960638/
Abstract

Measurable residual disease (MRD) is a powerful predictor of clinical outcomes in acute lymphoblastic leukemia (ALL). In addition to its clear prognostic importance, MRD information is increasingly used in clinical decision algorithms to guide therapeutic interventions. Although it is well established that achievement of MRD-negative remission is an important end point of ALL therapy, the prognostic and therapeutic implications of MRD in an individual patient are influenced by both disease-related factors (eg, cytomolecular risk) and assay-related factors (eg, sensitivity, specimen source, and timing of assessment), which add complexity to MRD-guided treatment decisions. In this review, we discuss the data supporting the use of MRD assessment in adult ALL and how this information can rationally inform clinical decisions, including selection of patients for MRD-directed therapies or allogeneic hematopoietic stem cell transplantation. We also discuss important interpretative challenges related to novel high sensitivity next-generation sequencing-based MRD assays, which are becoming increasingly used in clinical practice.

摘要

可测量残留病(MRD)是急性淋巴细胞白血病(ALL)临床结局的有力预测指标。除了其明确的预后重要性外,MRD信息在临床决策算法中越来越多地用于指导治疗干预。尽管已明确实现MRD阴性缓解是ALL治疗的一个重要终点,但个体患者中MRD的预后和治疗意义受疾病相关因素(如细胞分子风险)和检测相关因素(如敏感性、标本来源和评估时间)的影响,这增加了MRD指导治疗决策的复杂性。在本综述中,我们讨论了支持在成人ALL中使用MRD评估的数据,以及这些信息如何合理地为临床决策提供依据,包括选择接受MRD导向治疗或异基因造血干细胞移植的患者。我们还讨论了与新型高灵敏度下一代测序-based MRD检测相关的重要解释挑战,这些检测在临床实践中越来越多地被使用。