Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jul 15;105(26):2195-2202.
doi: 10.3760/cma.j.cn112137-20250226-00460.

[Predictive value of CT-based tumor and peritumoral radiomics for WHO/ISUP grading of non-metastatic clear cell renal cell carcinoma]

[Article in Chinese]
Affiliations

[Predictive value of CT-based tumor and peritumoral radiomics for WHO/ISUP grading of non-metastatic clear cell renal cell carcinoma]

[Article in Chinese]
J K Xu et al. Zhonghua Yi Xue Za Zhi. .

Abstract

Objective: To investigate the value of CT-based tumor and peritumoral radiomics in predicting the World Health Organization/International Society of Urological Pathology (WHO/ISUP) grading for non-metastatic clear cell renal cell carcinoma (ccRCC). Methods: A total of 503 patients with non-metastatic ccRCC were retrospectively enrolled from 7 tertiary hospitals between February 2017 and December 2023. Patients from 4 hospitals within Shandong Province were divided into a training set and an internal validation set in a 7∶3 ratio, while patients from 3 hospitals outside Shandong Province constituted the external validation set. Regions of interest (ROI) were manually delineated slice-by-slice along the tumor margin on contrast-enhanced CT images. Peritumoral regions were obtained by expanding 10 mm outward from the tumor boundary. Key radiomics features were selected using Least Absolute Shrinkage and Selection Operator (LASSO) regression with five-fold cross-validation to build tumor models and peritumoral models for predicting the WHO/ISUP grading. Univariate logistic regression was used to screen clinical factors associated with the WHO/ISUP grading, which was included to construct a combined predictive model together with tumor and peritumoral features. The predictive performance of the models for WHO/ISUP grading was evaluated using receiver operating characteristic (ROC) curves, and the Youden index and optimal cutoff value were calculated for risk stratification. Calibration curves were used to validate model performance, and decision curve analysis (DCA) was employed to evaluate the clinical value of the models. Results: The median age [M(Q1,Q3)] of the 503 patients was 59.0 (52.0, 66.0) years, with 335 males and 168 females. Univariate logistic regression analysis showed there was a statistically significance in age between low and high WHO/ISUP grades (P=0.043). The AUC of the tumor model and peritumoral model in the internal validation set were 0.744 (95%CI: 0.700-0.788) and 0.742 (95%CI: 0.709-0.774), respectively. In the external validation set, the AUC of the tumor model and peritumoral model were 0.685 (95%CI: 0.651-0.720) and 0.655 (95%CI: 0.628-0.683), respectively. The combined model demonstrated the best predictive performance in both internal and external validation sets, with AUC of 0.760 (95%CI: 0.721-0.800) and 0.706 (95%CI: 0.675-0.737), respectively. Using the Youden index calculated from the ROC curve from the combined model, the optimal cutoff value was 0.504 for risk stratification, where 190 cases were classified as low-grade and 313 as high-grade, achieving a concordance rate of 0.718 (361/503) with the WHO/ISUP grading. Calibration curve tests indicated good fit for the combined model (internal validation set: P=0.932; external validation set: P=0.404). DCA showed that the combined model provided favorable clinical net benefit within the threshold probability range of 0.2-0.8. Conclusion: The combined model incorporating age, CT-based tumor features, and peritumoral features demonstrates good performance in predicting the WHO/ISUP grading for patients with non-metastatic ccRCC.

目的: 探究基于CT肿瘤和瘤周影像组学在预测非转移性肾透明细胞癌(ccRCC)的世界卫生组织/国际泌尿病理学会(WHO/ISUP)分级的价值。 方法: 回顾性收集2017年2月至2023年12月7家三甲医院(北京3家,山东4家)共503例非转移性ccRCC患者,其中山东省内4家医院患者按照7∶3的比例分为训练集和内部验证集,山东省外3家医院患者作为外部验证集。在CT增强图像沿肿瘤边缘人工逐层勾画感兴趣区(ROI),向外膨胀10 mm获得瘤周区域。通过最小绝对收缩和选择算法(LASSO)回归及五折交叉验证筛选关键影像组学特征,构建预测WHO/ISUP分级的肿瘤模型和瘤周模型。分析WHO/ISUP分级相关的临床指标,并与肿瘤和瘤周组学特征共同构建联合模型。通过受试者工作特征(ROC)曲线评价模型对WHO/ISUP分级的预测效能,计算约登指数及最佳临界值对患者分层。采用校准曲线对模型效能进行验证、决策曲线(DCA)评估模型的临床价值。 结果: 503例患者的年龄[MQ1Q3)]为59.0(52.0,66.0)岁,男335例,女168例。低级别和高级别WHO/ISUP分级患者在年龄间差异具有统计学意义(P=0.043)。肿瘤模型和瘤周模型在内部验证集的曲线下面积(AUC)分别为0.744(95%CI:0.700~0.788)和0.742(95%CI:0.709~0.774),外部验证集的AUC分别为0.685(95%CI:0.651~0.720)和0.655(95%CI:0.628~0.683);联合模型在内外部验证集中均表现出最佳的预测性能,AUC分别为0.760(95%CI:0.721~0.800)和0.706(95%CI:0.675~0.737)。据联合模型的ROC曲线计算约登指数,以0.504为最佳临界值点进行危险分层,结果显示190例为低分级、313例为高分级,与WHO/ISUP分级一致性达0.718(361/503)。校准曲线检验结果显示联合模型拟合效果较好(内部验证集:P=0.932;外部验证集:P=0.404)。DCA结果显示,联合模型在阈值概率0.2~0.8时具有较好的临床净收益。 结论: 基于年龄、CT肿瘤和瘤周区域的联合模型在预测非转移性ccRCC患者的WHO/ISUP分级方面有良好的性能。.

PubMed Disclaimer

Similar articles

Publication types