TRACE模型:预测不可切除肝细胞癌经动脉化疗栓塞的治疗反应。

IF 4.2 3区 医学 Q2 ONCOLOGY
Journal of Hepatocellular Carcinoma Pub Date : 2025-01-29 eCollection Date: 2025-01-01 DOI:10.2147/JHC.S490226
Weilang Wang, Qi Zhang, Ying Cui, Shuhang Zhang, Binrong Li, Tianyi Xia, Yang Song, Shuwei Zhou, Feng Ye, Wenbo Xiao, Kun Cao, Yuan Chi, Jinrong Qu, Guofeng Zhou, Zhao Chen, Teng Zhang, Xunjun Chen, Shenghong Ju, Yuan-Cheng Wang
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引用次数: 0

摘要

目的:建立并验证一种预测模型,通过整合前处理MRI特征和TACE后1个月的治疗反应来预测6个月的预后。方法:对来自单臂多中心临床试验(NCT03113955)的108例160例hcc患者进行分析,并作为训练队列。外部多中心数据集(ChiCTR2100046020)包含63例99例hcc患者作为测试数据集。基于预处理后的MR图像所选择的特征构建放射组学模型。使用临床和放射学因素的单因素和多因素logistic回归分析来确定6个月治疗反应的独立预测因素。结合1个月的治疗反应、选定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。结果:在所有临床和放射学特征中,仅选择冠状增强和1个月治疗反应。联合模型命名为TRACE模型(1个月治疗反应、放射组学和冠状增强),auc为0.91(训练队列)和0.84(测试队列)。TRACE模型的AUC明显高于放射组学模型(P = 0.001)。采用TRACE模型分层的高危组和低危组的总生存期(OS)也有显著差异(P < 0.001)。相比之下,所有已发表的评分系统,包括ART、SNACOR或ABCR评分,都没有显示出风险组之间在OS预测方面的显著差异。结论:TRACE模型对6个月TACE反应表现出良好的预测能力,并有潜力作为长期生存结果的标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TRACE Model: Predicting Treatment Response to Transarterial Chemoembolization in Unresectable Hepatocellular Carcinoma.

Purpose: To develop and validate a predictive model for predicting six-month outcome by integrating pretreatment MRI features and one-month treatment response after TACE.

Methods: 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.

Results: 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 (P = 0.001). High-risk and low-risk groups stratified by using the TRACE model also exhibited significant differences in overall survival (OS) (P < 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.

Conclusion: The TRACE model exhibited favorable predictive capability for six-month TACE response, and holds potential as a marker for long-term survival outcomes.

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来源期刊
CiteScore
0.50
自引率
2.40%
发文量
108
审稿时长
16 weeks
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