Variable screening and model construction for prognosis of elderly patients with lower-grade gliomas based on LASSO-Cox regression: a population-based cohort study

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Xiaodong Niu, Tao Chang, Yuekang Zhang, Yanhui Liu, Yuan Yang, Qing Mao
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Abstract

BackgroundThis study aimed to identify prognostic factors for survival and develop a prognostic nomogram to predict the survival probability of elderly patients with lower-grade gliomas (LGGs).MethodsElderly patients with histologically confirmed LGG were recruited from the Surveillance, Epidemiology, and End Results (SEER) database. These individuals were randomly allocated to the training and validation cohorts at a 2:1 ratio. First, Kaplan−Meier survival analysis and subgroup analysis were performed. Second, variable screening of all 13 variables and a comparison of predictive models based on full Cox regression and LASSO-Cox regression analyses were performed, and the key variables in the optimal model were selected to construct prognostic nomograms for OS and CSS. Finally, a risk stratification system and a web-based dynamic nomogram were constructed.ResultsA total of 2307 elderly patients included 1220 males and 1087 females, with a median age of 72 years and a mean age of 73.30 ± 6.22 years. Among them, 520 patients (22.5%) had Grade 2 gliomas, and 1787 (77.5%) had Grade 3 gliomas. Multivariate Cox regression analysis revealed four independent prognostic factors (age, WHO grade, surgery, and chemotherapy) that were used to construct the full Cox model. In addition, LASSO-Cox regression analysis revealed five prognostic factors (age, WHO grade, surgery, radiotherapy, and chemotherapy), and a LASSO model was constructed. A comparison of the two models revealed that the LASSO model with five variables had better predictive performance than the full Cox model with four variables. Ultimately, five key variables based on LASSO-Cox regression were utilized to develop prognostic nomograms for predicting the 1-, 2-, and 5-year OS and CSS rates. The nomograms exhibited relatively good predictive ability and clinical utility. Moreover, the risk stratification system based on the nomograms effectively divided patients into low-risk and high-risk subgroups.ConclusionVariable screening based on LASSO-Cox regression was used to determine the optimal prediction model in this study. Prognostic nomograms could serve as practical tools for predicting survival probabilities, categorizing these patients into different mortality risk subgroups, and developing personalized decision-making strategies for elderly patients with LGGs. Moreover, the web-based dynamic nomogram could facilitate its use in the clinic.
基于 LASSO-Cox 回归的低级别胶质瘤老年患者预后变量筛选和模型构建:一项基于人群的队列研究
背景本研究旨在确定预后生存因素,并开发一种预后提名图来预测低级别胶质瘤(LGG)老年患者的生存概率。方法从监测、流行病学和最终结果(SEER)数据库中招募组织学确诊为低级别胶质瘤的老年患者。这些患者按 2:1 的比例随机分配到训练组和验证组。首先,进行卡普兰-梅耶生存分析和亚组分析。其次,对所有13个变量进行了筛选,并比较了基于完全Cox回归和LASSO-Cox回归分析的预测模型,选择了最佳模型中的关键变量,构建了OS和CSS的预后提名图。结果 共有 2307 名老年患者,其中男性 1220 人,女性 1087 人,中位年龄 72 岁,平均年龄(73.30±6.22)岁。其中,520 名患者(22.5%)为 2 级胶质瘤,1787 名患者(77.5%)为 3 级胶质瘤。多变量 Cox 回归分析显示了四个独立的预后因素(年龄、WHO 分级、手术和化疗),并以此构建了完整的 Cox 模型。此外,LASSO-Cox回归分析显示了五个预后因素(年龄、WHO分级、手术、放疗和化疗),并构建了一个LASSO模型。对这两个模型进行比较后发现,包含五个变量的 LASSO 模型比包含四个变量的完整 Cox 模型具有更好的预测效果。最终,基于LASSO-Cox回归的五个关键变量被用来绘制预后提名图,以预测1年、2年和5年的OS和CSS率。提名图显示了相对较好的预测能力和临床实用性。此外,基于提名图的风险分层系统有效地将患者分为低风险亚组和高风险亚组。预后提名图可以作为实用工具,用于预测生存概率,将这些患者分为不同的死亡风险亚组,并为老年 LGG 患者制定个性化的决策策略。此外,基于网络的动态预后提名图还能促进其在临床中的应用。
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
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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