建立两个同步多发性原发性肺癌患者的生存预测模型:多中心队列分析。

IF 4 2区 医学 Q2 ONCOLOGY Translational lung cancer research Pub Date : 2024-09-30 Epub Date: 2024-09-27 DOI:10.21037/tlcr-24-252
Ying Ji, Qing Zhao, Yi Liu, Bin Qiu, Guangyu Bai, Siyuan Ai, Wei Feng, Ligong Yuan, Xin Wang, Lulu Rong, Hua Fu, Huihui Xie, Linlin Qi, Ye Tao, Longyu Jin, Jing Zhou, Bin Hu, Shugeng Gao
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引用次数: 0

摘要

背景:同步多发原发性肺癌(SMPLC)的预后预测因素仍不明确,并且缺乏对SMPLC患者(不包括多灶性磨玻璃/鳞状结节(GG/L)患者)预后的研究。本研究的目的是建立一个有效的模型来预测SMPLC患者的生存率:在这项多中心队列研究中,共纳入了 2004 年 1 月至 2018 年 1 月在五家机构接受肺癌切除术的 831 例 SMPLC 患者,用于开发和验证提名图模型。其中,中国医学科学院肿瘤医院和首都医科大学附属北京朝阳医院的 499 例患者作为训练队列。中南大学湘雅三医院、中国科学技术大学附属第一医院和北京良乡医院的 332 名患者作为外部验证队列。在总生存率方面,将提名图模型与肿瘤结节转移(TNM)系统进行了比较。C指数、净再分类改进(NRI)和综合判别改进(IDI)被用来评估模型的性能。为了更好地了解切除的SMPLC患者的预后,该研究还提供了一个用户友好型网站,用于计算SMPLC的生存概率:结果:通过对训练集进行多变量分析,共筛选出七个独立的危险因素。结果:通过对训练集进行多变量分析,共筛选出七个独立的风险因素,并利用这些因素建立了一个提名图模型。内部和外部验证均显示出良好的区分度(C-指数:内部,0.827;外部,0.784)。该模型的 NRI 和 IDI 分别为 0.33 和 0.21。1 年、3 年和 5 年的存活率与实际观察值一致。通过将患者分为三个不同组别,确定了一组临界值。结论:新的提名图模型能准确预测患者的生存率:新颖的提名图模型可对切除的 SMPLC 患者进行准确的生存风险分层,并可协助做出有利于高风险 SMPLC 患者的决策。
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Establishment of a survival predictive model for patients with two synchronous multiple primary lung cancers: a multicenter cohort analysis.

Background: The prognostic predictors of the synchronous multiple primary lung cancer (SMPLC) still remain unclear, and there is a lack of studies on the prognosis of SMPLC patients excluding those with multifocal ground-glass/lepidic (GG/L) nodules. The aim of this study is to develop an effective model for predicting survival of SMPLC patients.

Methods: In this multicenter cohort study, a total of 831 SMPLC patients presenting for lung cancer resection from January 2004 to January 2018 at five institutions were included for developing and validating a nomogram model. Specifically, 499 patients from the Cancer Hospital, Chinese Academy of Medical Sciences, and Beijing Chao-Yang Hospital, Capital Medical University were served as the training cohort. A total of 332 patients from The Third Xiangya Hospital of Central South University, the First Affiliated Hospital of University of Science and Technology of China, and Beijing Liangxiang Hospital were served as the external validation cohort. The nomogram model was compared with the Tumor Node Metastasis (TNM) system for the overall survival. The C-index, net reclassification improvement (NRI), and integrated discrimination improvement (IDI) were used to evaluate the model performance. A user-friendly website for SMPLC survival probability calculation was also provided for a better understanding of prognosis of patients with resected SMPLC.

Results: A total of seven independent risk factors were selected by conducting a multivariate analysis on the training set. Further, a nomogram model was developed with these factors. Both the internal and external validations exhibited good discrimination (C-index: internal, 0.827; external, 0.784). The NRI and IDI of this model were 0.33 and 0.21, respectively. The survival rates for 1-year, 3-year, and 5-year were consistent with the actual observed values. A set of cutoff values were determined by grouping the patients into three different groups. For each group, we should expect a significant distinction between survival curves.

Conclusions: The novel nomogram model enables accurate survival risk stratification of patients with resected SMPLC and may assist in decision-making that is conducive to patients with SMPLC at high risk.

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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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