Predictive Model of Gemtuzumab Ozogamicin Response in Childhood Acute Myeloid Leukemia on Event-Free Survival: Data Analysis Based on Trial AAML0531.

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL Bioengineering Pub Date : 2025-03-14 DOI:10.3390/bioengineering12030297
Kun-Yin Qiu, Xiong-Yu Liao, Jian-Pei Fang, Dun-Hua Zhou
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Abstract

Purpose: We aimed to develop a simple nomogram and online calculator that can identify the optimal subpopulation of pediatric acute myeloid leukemia (AML) patients who would benefit most from gemtuzumab ozogamicin (GO) therapy. Methods: Within the framework of the phase Ⅲ AAML0531 randomized trial for GO, the event-free survival (EFS) probability was calculated using a predictor-based nomogram to evaluate GO treatment impact on EFS in relation to baseline characteristics. Nomogram performance was assessed by the area under the receiver operating characteristic curve (AUC) and the calibration curve with 500 bootstrap resample validations. Decision curve analysis (DCA) was performed to evaluate the clinical utility of the nomogram. Results: A total of 705 patients were randomly assigned to two arms: the No-GO arm (n = 358) and the GO arm (n = 347). We performed a nomogram model for EFS among childhood AML. The AUC (C statistic) of the nomogram was 0.731 (95%CI: 0.614-0.762) in the development group and 0.700 (95% CI: 0.506-0.889) in the validation group. DCA showed that the model in the development and validation groups had a net benefit when the risk thresholds were 0-0.75 and 0-0.75, respectively. Notably, an intriguing observation emerged wherein pediatric patients with AML exhibited a favorable outcome in the GO arm when the predicted 5-year EFS probability fell below 60%, demonstrating a superior EFS compared to the No-GO Arm. Conclusions: We have developed a nomogram and online calculator that can be used to predict EFS among childhood AML based on trial AAML0531, and this might help deciding which patients can benefit from GO.

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吉妥珠单抗Ozogamicin反应对儿童急性髓系白血病无事件生存的预测模型:基于试验AAML0531的数据分析
目的:我们旨在开发一种简单的nomogram和在线计算器,以确定从gemtuzumab ozogamicin (GO)治疗中获益最多的儿科急性髓性白血病(AML)患者的最佳亚群。方法:在ⅢAAML0531期氧化石墨烯随机试验的框架内,使用基于预测因子的nomogram来计算无事件生存(EFS)概率,以评估氧化石墨烯治疗对EFS与基线特征的影响。通过500次bootstrap重采样验证,通过受试者工作特征曲线(AUC)下面积和校准曲线来评估Nomogram性能。采用决策曲线分析(DCA)评价nomogram临床应用价值。结果:共有705名患者被随机分为两组:No-GO组(n = 358)和GO组(n = 347)。我们对儿童期AML患者的EFS进行了nomogram模型。发展组和验证组的nomogram AUC (C统计量)分别为0.731 (95%CI: 0.614 ~ 0.762)和0.700 (95%CI: 0.506 ~ 0.889)。DCA表明,当风险阈值分别为0-0.75和0-0.75时,开发组和验证组中的模型具有净收益。值得注意的是,一项有趣的观察结果显示,当预测的5年EFS概率低于60%时,氧化石墨烯组的儿科AML患者表现出有利的结果,表明与不氧化石墨烯组相比,氧化石墨烯组的EFS更优越。结论:基于试验AAML0531,我们开发了一种nomogram和在线计算器,可用于预测儿童AML患者的EFS,这可能有助于确定哪些患者可以从GO中受益。
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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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