Wang Weilang, Zhang Qi, Cui Ying, Zhang Shuhang, Li Binrong, Xia Tianyi, Song Yang, Zhou Shuwei, Ye Feng, Xiao Wenbo, Cao Kun, Chi Yuan, Qu Jinrong, Zhou Guofeng, Chen Zhao, Zhang Teng, Chen Xunjun, Ju Shenghong, Wang Yuan-Cheng
Department of Radiology, Zhongda Hospital, Nurturing Center of Jiangsu Province for State Laboratory of AI Imaging & Interventional Radiology, School of Medicine, Southeast University, Nanjing, 210009, People's Republic of China.
Center of Interventional Radiology and Vascular Surgery, Department of Radiology, Zhongda Hospital, Medical School, Southeast University, Nanjing, People's Republic of China.
J Hepatocell Carcinoma. 2025 Jan 29;12:193-203. doi: 10.2147/JHC.S490226. eCollection 2025.
To develop and validate a predictive model for predicting six-month outcome by integrating pretreatment MRI features and one-month treatment response after TACE.
A total of 108 patients with 160 hCCs from a single-arm, multicenter clinical trial (NCT03113955) were analyzed and served as the training cohort. An external multicenter dataset (ChiCTR2100046020) consisting of 63 patients with 99 hCCs served as the test dataset. Radiomics model was constructed based on the selected features from pretreatment MR images. Univariate and multivariate logistic regression analysis of clinical and radiological factors were used to identify the independent predictors for the 6-month treatment response. A combined model was further constructed by incorporating one-month treatment response, selected clinical and radiological factors and radiomics signature.
Among all the clinical and radiological features, only corona enhancement and one-month treatment response were selected. The combined model, named TRACE model (Treatment response at 1 month, RAdiomics and Corona Enhancement), with AUCs of 0.91 (training cohort) and 0.84 (test cohort). The TRACE model demonstrated a significantly higher AUC than the radiomics model ( = 0.001). High-risk and low-risk groups stratified by using the TRACE model also exhibited significant differences in overall survival (OS) ( < 0.001). In contrast, none of the published scoring systems, including ART, SNACOR or ABCR score, demonstrated significant differences between the risk groups in OS prediction.
The TRACE model exhibited favorable predictive capability for six-month TACE response, and holds potential as a marker for long-term survival outcomes.
通过整合TACE治疗前的MRI特征和1个月的治疗反应,开发并验证一种预测6个月预后的预测模型。
对来自一项单臂多中心临床试验(NCT03113955)的108例患者的160个肝细胞癌(hCC)进行分析,并作为训练队列。一个由63例患者的99个hCC组成的外部多中心数据集(ChiCTR2100046020)作为测试数据集。基于治疗前MR图像中选择的特征构建放射组学模型。采用临床和放射学因素的单因素和多因素逻辑回归分析,确定6个月治疗反应的独立预测因素。通过纳入1个月的治疗反应、选择的临床和放射学因素以及放射组学特征,进一步构建联合模型。
在所有临床和放射学特征中,仅选择了晕环强化和1个月的治疗反应。联合模型名为TRACE模型(1个月治疗反应、放射组学和晕环强化),训练队列的AUC为0.91,测试队列的AUC为0.84。TRACE模型的AUC显著高于放射组学模型(P = 0.001)。使用TRACE模型分层的高风险和低风险组在总生存期(OS)方面也表现出显著差异(P < 0.001)。相比之下,包括ART、SNACOR或ABCR评分在内的所有已发表的评分系统,在OS预测的风险组之间均未显示出显著差异。
TRACE模型对TACE治疗6个月的反应具有良好的预测能力,并且有潜力作为长期生存结果的标志物。