Hu Guangchao, Qu Jianyi, Gao Jie, Chen Yuqian, Wang Fang, Zhang Haicheng, Zhang Han, Wang Xuefeng, Ma Heng, Xie Haizhu, Xu Cong, Li Naixuan, Zhang Qianqian
Department of Radiology, Qingdao Municipal Hospital, Qingdao, Shandong, China.
Department of Radiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Front Oncol. 2024 Jul 11;14:1371432. doi: 10.3389/fonc.2024.1371432. eCollection 2024.
This study aimed to develop and validate a radiogenomics nomogram for predicting microvascular invasion (MVI) in hepatocellular carcinoma (HCC) on the basis of MRI and microRNAs (miRNAs).
This cohort study included 168 patients (training cohort: n = 116; validation cohort: n = 52) with pathologically confirmed HCC, who underwent preoperative MRI and plasma miRNA examination. Univariate and multivariate logistic regressions were used to identify independent risk factors associated with MVI. These risk factors were used to produce a nomogram. The performance of the nomogram was evaluated by receiver operating characteristic curve (ROC) analysis, sensitivity, specificity, accuracy, and F1-score. Decision curve analysis was performed to determine whether the nomogram was clinically useful.
The independent risk factors for MVI were maximum tumor length, rad-score, and miRNA-21 (all P < 0.001). The sensitivity, specificity, accuracy, and F1-score of the nomogram in the validation cohort were 0.970, 0.722, 0.884, and 0.916, respectively. The AUC of the nomogram was 0.900 (95% CI: 0.808-0.992) in the validation cohort, higher than that of any other single factor model (maximum tumor length, rad-score, and miRNA-21).
The radiogenomics nomogram shows satisfactory predictive performance in predicting MVI in HCC and provides a feasible and practical reference for tumor treatment decisions.
本研究旨在基于磁共振成像(MRI)和微小RNA(miRNA)开发并验证一种用于预测肝细胞癌(HCC)微血管侵犯(MVI)的放射基因组学列线图。
本队列研究纳入了168例经病理证实的HCC患者(训练队列:n = 116;验证队列:n = 52),这些患者均接受了术前MRI检查和血浆miRNA检测。采用单因素和多因素逻辑回归分析来确定与MVI相关的独立危险因素。这些危险因素被用于生成列线图。通过受试者操作特征曲线(ROC)分析、灵敏度、特异度、准确度和F1评分来评估列线图的性能。进行决策曲线分析以确定该列线图是否具有临床实用性。
MVI的独立危险因素为肿瘤最大径、放射组学评分和miRNA-21(均P < 0.001)。验证队列中列线图的灵敏度、特异度、准确度和F1评分分别为0.970、0.722、0.884和0.916。验证队列中列线图的AUC为0.900(95%CI:0.808 - 0.992),高于任何其他单一因素模型(肿瘤最大径、放射组学评分和miRNA-21)。
放射基因组学列线图在预测HCC的MVI方面表现出令人满意的预测性能,并为肿瘤治疗决策提供了可行且实用的参考。