基于炎症和临床病理因素的远处转移性 DTC 预后提名图模型

IF 3 Q2 ENDOCRINOLOGY & METABOLISM
Journal of the Endocrine Society Pub Date : 2025-02-27 eCollection Date: 2025-05-01 DOI:10.1210/jendso/bvaf037
Chenghui Lu, Guoqiang Wang, Zengmei Si, Fengqi Li, Xinfeng Liu, Na Han, Congcong Wang, Jiao Li, Xufu Wang
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引用次数: 0

摘要

背景:炎症标志物可作为预测远处转移分化型甲状腺癌(DM-DTC)患者预后的潜在生物标志物:本研究旨在评估炎症标志物和临床病理特征对DM-DTC患者疾病进展(PD)的预测能力:方法:对2016年5月至2022年1月期间的230例DM-DTC患者进行回顾性分析。患者按 7:3 的比例分为训练集和验证集。在最后一次131I治疗前1周内采集炎症标记物。主要结果是无进展生存期(PFS)。单变量和多变量 Cox 比例危险模型确定了重要的预后因素,基于炎症标志物和临床病理特征构建了一个提名图,并使用 R 软件进行了验证:多变量 Cox 回归分析显示,年龄(危险比 [HR] = 2.191; 95% CI, 1.387-3.462)、组织学类型(HR = 2.030; 95% CI, 1.216-3.389)、远处转移部位(HR = 3.379;95% CI,1.832-6.233)、T 期(HR = 6.061;95% CI,2.469-14.925)和 LMR(HR = 2.050;95% CI,1.194-3.519)被确定为 DM-DTC 进展的独立危险因素。我们构建了一个预测提名图来估算DM-DTC进展的概率。经计算,训练集的 PFS 模型 C 指数为 0.775(0.749-0.802),验证集为 0.731(95% CI,0.686-0.775)。验证集的校准曲线非常接近参考线。决策曲线分析表明,当风险阈值大于 0.2 时,该提名图模型可提供临床净效益:该研究确定了预测DM-DTC患者PD的重要炎症标志物和临床因素,提供了一个稳健的预后模型,具有潜在的临床应用价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nomogram Model for Prognosis of Distant Metastatic DTC Based on Inflammatory and Clinicopathological Factors.

Context: Inflammatory markers may serve as potential biomarkers in predicting prognosis in patients with distant metastasis differentiated thyroid cancer (DM-DTC).

Objective: This study aimed to evaluate the predictive ability of inflammatory markers and clinicopathological features for disease progression (PD) in patients with DM-DTC.

Methods: A retrospective analysis was conducted on 230 DM-DTC patients from May 2016 to January 2022. Patients were divided into a training set and a validation set at a 7:3 ratio. Inflammatory markers were obtained within 1 week before the last 131I treatment. The primary outcome was progression-free survival (PFS). Univariable and multivariable Cox proportional hazards models identified significant prognostic factors, and a nomogram based on inflammatory markers and clinicopathological features was constructed and validated using R software.

Results: Multivariable Cox regression analysis showed that age (hazard ratio [HR] = 2.191; 95% CI, 1.387-3.462), histological type (HR = 2.030; 95% CI, 1.216-3.389), distant metastatic site (HR = 3.379; 95% CI, 1.832-6.233), T stage (HR = 6.061; 95% CI, 2.469-14.925), and LMR (HR = 2.050; 95% CI, 1.194-3.519) were identified as independent risk factors for the progression of DM-DTC. A predictive nomogram was constructed to estimate the probability of DM-DTC progression. The C-index of the PFS model was calculated to be 0.775 (0.749-0.802) for the training set and 0.731 (95% CI, 0.686-0.775) for the validation set. The calibration curve of the validation set closely approached the reference line. The decision curve analysis indicated that when the risk threshold was greater than 0.2, this nomogram model provided clinical net benefit.

Conclusion: The study identified significant inflammatory markers and clinical factors for predicting PD in DM-DTC patients, providing a robust prognostic model with potential clinical application.

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来源期刊
Journal of the Endocrine Society
Journal of the Endocrine Society Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.50
自引率
0.00%
发文量
2039
审稿时长
9 weeks
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