新诊断急性髓系白血病行异基因造血干细胞移植后缓解诱导后早期WT1 mRNA减少的临床结果

IF 3.6 3区 医学 Q2 HEMATOLOGY Transplantation and Cellular Therapy Pub Date : 2025-03-01 DOI:10.1016/j.jtct.2024.12.007
Takafumi Tsushima, Chiharu Kimeda, Natsumi Yoda, Kosuke Matsuo, Kazusuke Tanaka, Yasuhito Hatanaka, Rena Matsumoto, Sonoko Shimoji, Yoshikazu Utsu, Shin-Ichi Masuda, Nobuyuki Aotsuka
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摘要

背景:Wilms' Tumor (WT1) mRNA是急性髓性白血病(AML)中可测量的残留疾病的非特异性标志物。很少有研究关注接受移植治疗的AML患者初始缓解诱导后WT1 mRNA的预后价值。目的:因此,我们回顾性分析我院AML患者初始缓解诱导后WT1 mRNA降低的临床特征及对预后的影响。我们使用对数分层对WT1 mRNA水平的降低进行分类,特别关注初始缓解诱导后3对数降低对预后的影响。研究设计:这项单中心、回顾性、观察性研究纳入了71例在2013年4月至2023年6月期间接受同种异体造血干细胞移植(alloo - hsct)的AML患者,并对WT1 mRNA进行了量化。结果:根据随访中是否观察到3对数下降(N=30) (N=41)对患者进行分组。在未达到3 log降低的患者中,欧洲白血病网(ELN) 2022不良风险更常见,移植时出现完全血液学反应的患者更少。在初始缓解诱导后,WT1 mRNA达到3对数降低的患者与未达到3对数降低的患者相比,总生存期(OS)和无进展生存期(PFS)明显更长,复发率更低(2年OS: 79.7% vs. 27.5%, 2年PFS: 83.1% vs. 11.7%, 2年累积复发率:5.9% vs. 81.2%)。在多变量分析中,初始缓解诱导后WT1 mRNA的3对数降低和遗传导致的ELN 2022不良风险与OS和PFS显著相关。结论:我们发现接受HSCT的AML患者在初始缓解诱导后WT1 mRNA早期和深度3-log降低与低复发率和更好的长期预后相关。我们的数据强调了初始缓解诱导后WT1 mRNA减少的重要性。
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Clinical Outcomes of Early WT1 mRNA Reduction After Remission Induction in Newly Diagnosed Acute Myeloid Leukemia Undergoing Allogeneic Hematopoietic Stem Cell Transplantation
Wilms’ Tumor 1 (WT1) mRNA is a non-specific marker of measurable residual disease in acute myeloid leukemia (AML). Few studies have focused on the prognostic value of WT1 mRNA after initial remission induction of patients with AML who have received transplant treatments. Thus, we retrospectively analyzed the clinical features and prognostic impact of WT1 mRNA reduction in patients with AML after initial remission induction at our hospital. We classified the reduction in WT1 mRNA levels using logarithmic stratification, with particular focus on the prognostic impact of a 3-log reduction after initial remission induction. This single-center, retrospective, observational study included 71 consecutive patients with AML who underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT) between April 2013 and June 2023 and had WT1 mRNA quantified. Patients were grouped based on whether a 3-log reduction was observed during follow-up (N=30) or not (N=41). Among patients who did not achieve a 3-log reduction, European Leukemia Net (ELN) 2022 adverse risk was more common, and fewer patients showed complete hematological responses at transplantation. Patients who reached a 3-log reduction in WT1 mRNA after the initial remission induction had significantly longer overall survival (OS) and progression-free survival (PFS) and a lower relapse rate than patients who had not reached a 3-log reduction (2-year OS: 79.7% vs. 27.5%, 2-year PFS: 83.1% vs. 11.7% and 2-year cumulative relapse rate: 5.9% vs. 81.2%). In multivariate analysis, a 3-log reduction in WT1 mRNA after initial remission induction and ELN 2022 adverse risk by genetics were significantly associated with OS and PFS. We identified that patients with AML undergoing HSCT with an early and deep 3-log reduction in WT1 mRNA after initial remission induction were associated with low relapse rates and better long-term prognosis. Our data highlight the importance of WT1 mRNA reduction after initial remission induction.
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CiteScore
7.00
自引率
15.60%
发文量
1061
审稿时长
51 days
期刊最新文献
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