胃癌预测模型的开发与验证:一项单中心前瞻性研究。

Suyu Sun, Feifei Huang, Xueqin Xu, Ke Xu, Tingting Peng, Wenjing Bai, Chunwei Huang, Xingzhong Hu, Yong Pan
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引用次数: 0

摘要

目的:本研究旨在开发和验证诊断胃癌(GC)的新型提名图:本研究旨在开发和验证诊断胃癌(GC)的新型提名图:在这项前瞻性分析中,温州市中心医院招募了146名患者,分为胃癌组和良性病变组,并按7:3的比例分为训练集和内部验证集。收集临床和分析特征,并通过逻辑回归分析进行分析。使用接收者操作特征曲线、校准曲线和决策曲线分析评估了预测模型的性能:结果:白蛋白、癌胚抗原、125 碳水化合物抗原、肌酐和富含脯氨酸的小蛋白 2A 这 5 个变量被确定为所开发模型的最终参数。在训练集和内部验证集中,模型的曲线下面积分别为 0.968 和 0.979,显示出良好的诊断性能:本研究开发并验证了基于 5 个参数的新提名图。该模型在区分 GC 和良性病变组方面表现出良好的诊断性能,在临床应用中具有一定的意义。
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Development and validation of a prediction model for gastric cancer: a single-center prospective study.

Objective: This study aimed to develop and validate a novel nomogram for diagnosing gastric cancer (GC).

Methods: In this prospective analysis, 146 patients of Wenzhou Central Hospital were recruited for a GC group and a benign lesion group and were divided into a training set and an internal validation set in a ratio of 7:3. Clinical and analytical characteristics were collected and analyzed by logistic regression analysis. The performance of the predictive model was evaluated using the receiver operating characteristic curve, calibration curve, and decision curve analysis.

Results: There were 5 variables, namely albumin, carcinoembryonic antigen, carbohydrate antigen 125, creatinine, and small proline-rich protein 2A, that were identified as the final parameters for the developed model. In the training and internal validation sets, the area under the curve of the model was 0.968 and 0.979, respectively, showing good diagnostic performance.

Conclusion: This study developed and validated a new nomogram based on 5 parameters. This model shows good diagnostic performance in distinguishing GC from benign lesion groups and has certain significance in clinical application.

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