小儿急性髓性白血病干细胞移植的简化稳健风险分层模型。

IF 11.7 1区 医学 Q1 CELL BIOLOGY
Cell Reports Medicine Pub Date : 2024-10-15 Epub Date: 2024-10-03 DOI:10.1016/j.xcrm.2024.101762
Hua Yang, Yang Xun, Yali Shen, Hongtao Wang, Yu Tao, Huihan Wang, Xinyue Zhang, Rongqiu Liu, Huarong Yu, Li Wei, Jinsong Yan, Xiaoyu Zhu, Hua You
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引用次数: 0

摘要

由于现有预后模型在预测疗效和选择合适候选者方面的局限性,干细胞移植(SCT)在小儿急性髓性白血病(pAML)中的疗效仍不令人满意。本研究旨在为处于CR1阶段的pAML患者建立一个独立于细胞分子风险分层的SCT预后模型。该 pAML SCT 模型基于年龄、KMT2A 重排(KMT2A-r)和病程 1 结束时的最小残留病(MRD1),能有效地将患者分为低、中、高风险组。我们在一个内部验证队列和四个外部验证队列(包括不同的移植物来源和供体)中验证了该方法的有效性。此外,通过纳入FMS类酪氨酸激酶3/内部串联重复(FLT3/ITD)等位基因比率,pAML SCT模型得到了改进,提高了有效选择合适候选者的能力。我们为接受 SCT 的 pAML 患者建立了一个简单而稳健的风险分层模型,以帮助进行风险分层,并为 CR1 阶段的移植前决策提供依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A simplified and robust risk stratification model for stem cell transplantation in pediatric acute myeloid leukemia.

The efficacy of stem cell transplantation (SCT) in pediatric acute myeloid leukemia (pAML) remains unsatisfactory due to the limitations of existing prognostic models in predicting efficacy and selecting suitable candidates. This study aims to develop a cytomolecular risk stratification-independent prognostic model for SCT in pAML patients at CR1 stage. The pAML SCT model, based on age, KMT2A rearrangement (KMT2A-r), and minimal residual disease at end of course 1 (MRD1), effectively classifies patients into low-, intermediate-, and high-risk groups. We validate the effectiveness in an internal validation cohort and in four external validation cohorts, consisting of different graft sources and donors. Moreover, by incorporating the FMS-like tyrosine kinase 3/internal tandem duplication (FLT3/ITD) allelic ratio, the pAML SCT model is refined, enhancing its ability to effectively select suitable candidates. We develop a simple and robust risk stratification model for pAML patients undergoing SCT, to aid in risk stratification and inform pretransplant decision-making at CR1 stage.

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来源期刊
Cell Reports Medicine
Cell Reports Medicine Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
15.00
自引率
1.40%
发文量
231
审稿时长
40 days
期刊介绍: Cell Reports Medicine is an esteemed open-access journal by Cell Press that publishes groundbreaking research in translational and clinical biomedical sciences, influencing human health and medicine. Our journal ensures wide visibility and accessibility, reaching scientists and clinicians across various medical disciplines. We publish original research that spans from intriguing human biology concepts to all aspects of clinical work. We encourage submissions that introduce innovative ideas, forging new paths in clinical research and practice. We also welcome studies that provide vital information, enhancing our understanding of current standards of care in diagnosis, treatment, and prognosis. This encompasses translational studies, clinical trials (including long-term follow-ups), genomics, biomarker discovery, and technological advancements that contribute to diagnostics, treatment, and healthcare. Additionally, studies based on vertebrate model organisms are within the scope of the journal, as long as they directly relate to human health and disease.
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