Machine learning-based early prediction of severe pneumonia risk in hospitalized leukemia patients: a dual-center retrospective cohort study.

IF 5.3 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2026-09-18 eCollection Date: 2026-01-01 DOI:10.3389/fcell.2026.1943797
Jian Huang, Qinliang Wu, Yixin Zhang, Kai Wang, Yuanyuan Wang, Chaogui Tang, Chang Li, Ning Lin
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引用次数: 0

Abstract

Background: Severe pneumonia is a major infectious complication in patients with leukemia and may rapidly progress to respiratory failure or septic shock. Disease- and treatment-related immunosuppression increases susceptibility, yet population-specific early risk-stratification tools are limited.

Objectives: To develop and externally validate a machine learning model for predicting severe pneumonia in hospitalized patients with leukemia.

Methods: Data from 2,978 leukemia patients at two Chinese hospitals were retrospectively analyzed. The derivation cohort was divided into training and internal test sets; SMOTE was applied only to the training set. LASSO and SVM-RFE were used for predictive feature selection, eight machine learning algorithms were compared, and RCS was used for exploratory association analysis. The final model was presented as a nomogram.

Results: Seven predictors were retained: age, history of myelosuppression, acute lymphoblastic leukemia (ALL) subtype, cardiac insufficiency, atrial fibrillation, red blood cell distribution width-standard deviation (RDW-SD), and prothrombin time activity. Logistic regression showed the best generalizability, with an area under the curve (AUC) of 0.801 in external validation. Sensitivity analyses showed similar discrimination with multiple imputation and complete-case analysis.

Conclusion: We developed and externally validated an interpretable model for severe pneumonia in hospitalized patients with leukemia. Because direct programmed-cell-death biomarkers were not measured and SMOTE substantially altered training prevalence, mechanistic interpretation and absolute-risk calibration require caution. Prospective recalibration and clinical-impact evaluation are needed before routine use.

基于机器学习的白血病住院患者重症肺炎风险早期预测:一项双中心回顾性队列研究
背景:严重肺炎是白血病患者的主要感染性并发症,可迅速发展为呼吸衰竭或感染性休克。疾病和治疗相关的免疫抑制增加了易感性,但针对人群的早期风险分层工具有限。目的:开发并外部验证用于预测白血病住院患者重症肺炎的机器学习模型。方法:回顾性分析国内两所医院2978例白血病患者的资料。衍生队列分为训练集和内部测试集;SMOTE仅应用于训练集。采用LASSO和SVM-RFE进行预测特征选择,比较8种机器学习算法,采用RCS进行探索性关联分析。最后的模型以nomogram表示。结果:保留了7个预测因子:年龄、骨髓抑制史、急性淋巴细胞白血病(ALL)亚型、心功能不全、心房颤动、红细胞分布宽度-标准差(RDW-SD)和凝血酶原时间活性。Logistic回归的推广效果最好,外部验证的曲线下面积(AUC)为0.801。敏感性分析显示多重归算和全病例分析有相似的区别。结论:我们开发并外部验证了一个可解释的白血病住院患者重症肺炎模型。由于没有测量直接的程序性细胞死亡生物标志物,并且SMOTE大大改变了训练流行率,因此机制解释和绝对风险校准需要谨慎。在常规使用前需要进行前瞻性重新校准和临床影响评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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