基于双能 CT 导出的细胞外体积分数的预测胃癌微卫星不稳定性状态的提名图

Wenjun Hu, Ying Zhao, Hongying Ji, Anliang Chen, Qihao Xu, Yi-jun Liu, Ziming Zhang, Ailian Liu
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引用次数: 0

摘要

目的:开发并验证一种基于双能CT(DECT)得出的细胞外体积(ECV)分数的提名图,用于术前预测胃癌(GC)的微卫星不稳定性(MSI)状态。根据术后免疫组化染色将患者分为MSI组(41人)和微卫星稳定性组(82人),然后随机分配到训练组(86人)和验证组(37人)。我们提取了三个增强阶段的临床病理特征、CT成像特征、碘浓度(ICs)和针对主动脉的归一化IC值(nICs)。计算平衡期碘密度图得出的 ECV 分数。采用单变量和多变量逻辑回归分析来确定 MSI 状态的独立风险预测因素。然后,建立了一个提名图,并通过 ROC 分析和 Delong 检验对其性能进行了评估。ECV分数、肿瘤位置和Borrmann类型是MSI状态的独立预测因素(均P<0.05),并被用于建立提名图。在训练组和验证组中,提名图的AUC值分别为0.826(0.729-0.899)和0.833(0.675-0.935),高于单一变量(P<0.05),具有良好的校准性和临床实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nomogram based on dual-energy CT-derived extracellular volume fraction for the prediction of microsatellite instability status in gastric cancer
To develop and validate a nomogram based on extracellular volume (ECV) fraction derived from dual-energy CT (DECT) for preoperatively predicting microsatellite instability (MSI) status in gastric cancer (GC).A total of 123 patients with GCs who underwent contrast-enhanced abdominal DECT scans were retrospectively enrolled. Patients were divided into MSI (n=41) and microsatellite stability (MSS, n=82) groups according to postoperative immunohistochemistry staining, then randomly assigned to the training (n=86) and validation cohorts (n=37). We extracted clinicopathological characteristics, CT imaging features, iodine concentrations (ICs), and normalized IC values against the aorta (nICs) in three enhanced phases. The ECV fraction derived from the iodine density map at the equilibrium phase was calculated. Univariate and multivariable logistic regression analyses were used to identify independent risk predictors for MSI status. Then, a nomogram was established, and its performance was evaluated by ROC analysis and Delong test. Its calibration performance and clinical utility were assessed by calibration curve and decision curve analysis, respectively.The ECV fraction, tumor location, and Borrmann type were independent predictors of MSI status (all P < 0.05) and were used to establish the nomogram. The nomogram yielded higher AUCs of 0.826 (0.729–0.899) and 0.833 (0.675–0.935) in training and validation cohorts than single variables (P<0.05), with good calibration and clinical utility.The nomogram based on DECT-derived ECV fraction has the potential as a noninvasive biomarker to predict MSI status in GC patients.
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