通过机器学习分析预测费城染色体样急性淋巴细胞白血病的生存:一项多中心队列研究。

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2025-09-18 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1650810
Xiao-Dan Song, Dan-Na Lin, Lv-Hong Xu, Li-Ying Liu, Chi-Kong Li, Xiao-Rong Lai, Ya-Ting Zhang, Wu-Qing Wan, Xiao-Li Zhang, Xiang Lan, Xing-Jiang Long, Bei-Yan Wu, Qi-Wen Chen, Li-Hua Yang, Yun-Yan He
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引用次数: 0

摘要

背景:本研究旨在建立一种预测费城染色体样急性淋巴细胞白血病(ALL)患者无事件生存期(EFS)的有效生存模型。方法:收集2016年10月至2021年7月华南儿童白血病组(SCCLG)多中心研究中与ph样ALL相关的数据。使用Cox比例风险回归、随机森林、极端梯度增强和梯度增强机技术建立预测ph样ALL患者生存的模型。通过整合一致性指数(C-index)、1年、3年、5年受者下面积工作特征曲线(AUROC)、Brier评分、决策曲线分析等指标,比较各模型的预测能力。结果:随机森林算法表现出最稳健的预测性能。在检验集中,随机森林模型的c指数为0.797 (95% CI: 0.736-0.821; P < 0.001)。1年、3年和5年的auroc分别为0.787 (95% CI: 0.62-0.953; P < 0.001)、0.797 (95% CI: 0.589-1; P < 0.001)和0.861 (95% CI: 0.606-1; P < 0.001)。1年、3年和5年Brier评分分别为0.102 (95% CI: 0.032-0.173; P < 0.001)、0.126 (95% CI: 0.063-0.19; P < 0.001)和0.121 (95% CI: 0.051-0.19; P < 0.001)。结论:随机森林模型能有效预测ph样ALL患者的生存结局,有助于临床医生提前进行个性化的预后评估。基于网络计算器,使用随机森林预测模型计算ph样ALL的预后(https://songxiaodan03.shinyapps.io/RFpredictionmodelforPHlikeALL/),方便医护人员进行临床评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Survival prediction for Philadelphia chromosome-like acute lymphoblastic leukemia by machine learning analysis: a multicenter cohort study.

Survival prediction for Philadelphia chromosome-like acute lymphoblastic leukemia by machine learning analysis: a multicenter cohort study.

Survival prediction for Philadelphia chromosome-like acute lymphoblastic leukemia by machine learning analysis: a multicenter cohort study.

Survival prediction for Philadelphia chromosome-like acute lymphoblastic leukemia by machine learning analysis: a multicenter cohort study.

Background: This study aimed to develop an efficient survival model for predicting event-free survival (EFS) in patients with Philadelphia chromosome (Ph)-like acute lymphoblastic leukemia (ALL).

Methods: Data related to Ph-like ALL were collected from the South China Children's Leukemia Group (SCCLG) multicenter study conducted from October 2016 to July 2021. A model for predicting the survival of patients with Ph-like ALL was built using Cox proportional hazards regression, random forest, extreme gradient boosting, and gradient boosting machine techniques. By integrating indicators including the concordance index (C-index), 1-, 3-, and 5-year area-under-the-receiver operating characteristics curve (AUROC), Brier score, and decision curve analysis, the predictive capabilities of each model were compared.

Results: The random forest algorithm demonstrated the most robust predictive performance. In the test set, the C-index of the random forest model was 0.797 (95% CI: 0.736-0.821; P < 0.001). The AUROCs for 1, 3, and 5 years were 0.787 (95% CI: 0.62-0.953; P < 0.001), 0.797 (95% CI: 0.589-1; P < 0.001), and 0.861 (95% CI: 0.606-1; P < 0.001), respectively. The Brier scores for 1, 3, and 5 years were 0.102 (95% CI: 0.032-0.173; P < 0.001), 0.126 (95% CI: 0.063-0.19; P < 0.001), and 0.121 (95% CI: 0.051-0.19; P < 0.001), respectively.

Conclusion: The random forest model effectively predicted the survival outcomes of patients with Ph-like ALL, which can aid clinicians to conduct personalized prognosis assessments in advance. Based on a web-based calculator, using random forest prediction models to calculate the prognosis of Ph-like ALL (https://songxiaodan03.shinyapps.io/RFpredictionmodelforPHlikeALL/) could facilitate healthcare professionals in carrying out clinical evaluation.

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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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