基于提名图的淋巴瘤患者初期不明原因发热预后模型

IF 4.2 2区 医学 Q2 IMMUNOLOGY Journal of Inflammation Research Pub Date : 2024-11-07 eCollection Date: 2024-01-01 DOI:10.2147/JIR.S493158
Lin Shen, Wenjing Young, Min Wu, Yanhui Xie
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引用次数: 0

摘要

背景:以不明原因发热(FUO)为首发症状的淋巴瘤患者缺乏特定的临床特征分析、预后因素分析和现有的预后模型。我们旨在为这些患者建立一个预后模型,以改善预后和风险评估:方法:在复旦大学附属华东医院共研究了555例以FUO为首发症状的淋巴瘤患者。单变量 Cox 回归确定了结果预测因素,并通过 LASSO Cox 进行分析。多因素 Cox 筛选系数确定了独立的预后因素和提名图模型。通过自举取样、校准曲线进行模型校准、时间依赖性 ROC 曲线分析进行鉴别评估以及决策曲线分析评估临床实用性,对提名图的有效性进行了评估。进一步的验证包括使用 Kaplan-Meier 曲线和对数秩检验。最后,X-tile 软件通过与传统的国际预后指数(IPI)评分系统进行比较,确定了提名图评分的最佳临界点:整个队列被分为训练队列(388 人)和验证队列(167 人)。这些风险因素(细胞病理类型、表现状态评分、Ann Arbor分期、血小板减少症和直接胆红素升高)被用于为最初出现FUO的淋巴瘤患者构建基于网络的动态生存率计算器。淋巴瘤特异性提名图在预测模型的风险分层方面表现出良好的一致性和有效性。与IPI评分系统相比,提名图模型对不同临床终点的AUC值更高。与传统的IPI评分相比,新的提名图预后模型能更好地区分风险组别:我们的研究开发并验证了淋巴瘤初诊 FUO 患者的预后提名图,显示了强大的预测功效和风险分层能力。此外,我们还成功地将这一模型应用到了基于网络的动态生存率计算器中。
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A Nomogram-Based Prognostic Model for Lymphoma Patients Initially Presenting with Fever of Unknown Origin.

Background: Patients with lymphoma who present with fever of unknown origin (FUO) as an initial symptom lack specific clinical feature analysis, prognostic factor analysis, and existing prognostic models. We aim to create a prognostic model for these patients to improve prognosis and risk assessment.

Methods: A total of 555 lymphoma patients with FUO as initial symptom studied at Huadong Hospital affiliated with Fudan University. Univariable Cox regression identified outcome predictors, analyzed by LASSO Cox. Multifactorial Cox on screened coefficients determined independent prognostic factors and nomogram model. The validity of the nomogram was evaluated through bootstrap sampling, calibration curves for model calibration, time-dependent ROC curve analysis for discrimination assessment, and decision curve analysis for evaluating clinical usefulness. Further validation involved utilizing Kaplan-Meier curves and Log rank tests. Lastly, X-tile software determined the optimal cutoff point for the nomogram score by comparing it with the traditional International Prognostic Index (IPI) scoring system.

Results: The entire cohort was divided into a training cohort (n=388) and a validation cohort (n=167). These risk factors (cell pathologic type, performance status score, Ann Arbor staging, thrombocytopenia, and raised direct bilirubin) were used to construct a web-based dynamic survival rate calculator for lymphoma patients initially presenting with FUO. The lymphoma-specific nomogram demonstrated good consistency and efficacy in predicting the model's risk stratification. Compared to the IPI scoring system, the nomogram model had higher AUC values for different clinical endpoints. The new nomogram prognostic model showed better differentiation of risk groups compared to traditional IPI scoring.

Conclusion: Our study developed and validated a prognostic nomogram for lymphoma patients initially presenting with FUO, demonstrating robust predictive efficacy and risk stratification ability. Furthermore, we have successfully implemented this model into a web-based dynamic survival rate calculator.

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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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