通过倾向评分匹配预测肝内胆管癌患者肝切除术后的预后:竞争风险模型分析。

IF 1.5 4区 医学 Q4 ONCOLOGY
Translational cancer research Pub Date : 2025-03-30 Epub Date: 2025-03-25 DOI:10.21037/tcr-24-1819
Shu-Sen Jiang, Zhi-Yu Wang, Li-Jun Tan, Li-Xia Zhou, Xue-Yao Wang, Xin-Meng Han, Shun-Gang Li, Ji-Meng Luo, Hong-Bing Yao
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引用次数: 0

摘要

背景:肝切除术是肝内胆管癌(ICCA)的基础治疗方法;然而,利用相互竞争的风险模型对ICCA患者预后的研究仍然很少。本研究旨在建立一个利用竞争风险分析预测ICCA患者术后癌症特异性生存(CSS)的预后模型。方法:本研究回顾性分析了监测、流行病学和最终结果(SEER)数据库(2004-2015)中接受肝切除术的ICCA患者。患者被随机分配到训练组(70%)和验证组(30%),基线通过倾向评分匹配(PSM)平衡。通过竞争风险的单变量和多变量分析确定预后因素,促进相关风险模型和nomogram的发展。通过受试者工作特征(ROC)曲线、曲线下面积(AUC)和标定图评估模型的疗效,通过决策曲线分析(DCA)评估模型的临床效用。X-tile程序有助于根据从nomogram得出的分数将参与者分为低、中、高风险组。结果:在PSM后纳入分析的1131名参与者中,65.34% (n=739)死于ICCA, 13.97% (n=158)死于其他原因。ICCA患者肝切除术后1年、2年和3年总生存率(OS)分别为79.4%、59.8%和46.4%;相应的CSS率分别为82.5%、64.0%和51.3%。多因素分析显示,低分化、晚期T分期、淋巴结浸润和远处转移是重要的危险因素。训练队列1年、2年和3年预测CSS的auc分别为0.668、0.711和0.710。同样,测试队列1年、2年和3年的auc分别为0.709、0.718和0.721。AUC表明,所建立的nomogram模型具有中等的区分能力。标定曲线表明,预测值与实际数据吻合较好。与肿瘤淋巴结转移(TNM)分类系统相比,DCA显示出更大的临床应用价值。根据nomogram将患者分为3个风险组,结果显示各组患者的生存率存在显著差异(p)。结论:基于竞争风险模型的预后nomogram对ICCA患者肝切除术后的具体生存率具有中等的预测准确性,为个体化预测和治疗方案提供了实用的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prediction of the prognosis of intrahepatic cholangiocarcinoma patients after hepatectomy via propensity score matching: a competitive risk model analysis.

Background: Hepatectomy represents the cornerstone therapeutic approach for intrahepatic cholangiocarcinoma (ICCA); however, research pertaining to the prognosis of ICCA patients utilizing competing risk models remains scarce. This study aimed to construct a prognostic model utilizing competing risk analysis to predict cancer-specific survival (CSS) among ICCA patients posthepatectomy.

Methods: This study retrospectively analyzed ICCA patients from the Surveillance, Epidemiology, and End Results (SEER) database (2004-2015) who underwent hepatectomy. Patients were randomly allocated to the training (70%) and validation (30%) cohorts, with baselines balanced via propensity score matching (PSM). Prognostic factors were ascertained through both univariate and multivariate analyses of competing risks, facilitating the development of pertinent risk models and nomograms. The efficacy of the model was assessed via receiver operating characteristic (ROC) curves, area under the curve (AUC), and calibration plots, with clinical utility appraised through decision curve analysis (DCA). The X-tile program facilitated the categorization of participants into low-, intermediate-, and high-risk groups on the basis of their scores derived from the nomogram.

Results: Among the 1,131 participants included in the analysis after PSM, 65.34% (n=739) died from ICCA, and 13.97% (n=158) died from other causes. The 1-, 2-, and 3-year overall survival (OS) rates for ICCA patients after hepatectomy were 79.4%, 59.8% and 46.4%, respectively; the corresponding CSS rates were 82.5%, 64.0%, and 51.3%, respectively. Multivariate analysis revealed that hypodifferentiation, advanced T stage, lymph node invasion, and distant metastasis were significant risk factors. The AUCs for predicting CSS in the training cohort were 0.668, 0.711, and 0.710 for 1, 2, and 3 years, respectively. similarly, the AUCs for the test cohort were 0.709, 0.718, and 0.721 for 1, 2, and 3 years, respectively. The AUC demonstrated that the developed nomogram model exhibited moderate discriminatory power. The calibration curve demonstrated that the predicted values closely matched the actual data. DCA demonstrated greater clinical utility for the nomogram than the tumor node metastasis (TNM) classification system. Patients were divided into three risk groups according to the nomogram, which revealed substantial differences in survival rates between the groups (P<0.001).

Conclusions: The prognostic nomogram developed based on the competitive risk model demonstrates moderate predictive accuracy for the specific survival rate of ICCA patients after hepatectomy, offering a practical tool for individualized prognostication and treatment planning.

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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
252
期刊介绍: Translational Cancer Research (Transl Cancer Res TCR; Print ISSN: 2218-676X; Online ISSN 2219-6803; http://tcr.amegroups.com/) is an Open Access, peer-reviewed journal, indexed in Science Citation Index Expanded (SCIE). TCR publishes laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer; results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of cancer patients. The focus of TCR is original, peer-reviewed, science-based research that successfully advances clinical medicine toward the goal of improving patients'' quality of life. The editors and an international advisory group of scientists and clinician-scientists as well as other experts will hold TCR articles to the high-quality standards. We accept Original Articles as well as Review Articles, Editorials and Brief Articles.
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