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经动脉化疗栓塞术联合靶向和免疫治疗对比单纯经动脉化疗栓塞术可改善伴有微血管侵犯的肝细胞癌患者的无病生存期:一项多中心倾向评分匹配研究

Combined TACE with Targeted and Immunotherapy versus TACE Alone Improves DFS in HCC with MVI: A Multicenter Propensity Score Matching Study.

作者信息

Chen Xiaokun, Wu Xiangan, Peng Wei, Liu Liguo, Liu Xiao, Wan Xueshuai, Xu Haifeng, Zheng Yongchang, Zhao Haitao, Mao Yilei, Lu Xin, Sang Xinting, Chang Xiaoyan, Zhou Kang, Pan Jie, Guan Mei, Hu Dandan, Tan Haidong, Zhang Yaojun, Du Shunda

机构信息

Department of Liver Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, 100005, People's Republic of China.

Graduate School, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, 100006, People's Republic of China.

出版信息

J Hepatocell Carcinoma. 2025 Mar 19;12:561-577. doi: 10.2147/JHC.S504016. eCollection 2025.

DOI:10.2147/JHC.S504016
PMID:40124969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11930282/
Abstract

BACKGROUND

Hepatocellular carcinoma (HCC) with microvascular invasion (MVI) is associated with high recurrence and poor survival outcomes. Although adjuvant therapies such as transcatheter arterial chemoembolization (TACE), targeted therapy, and immunotherapy show potential in improving outcomes, the optimal postoperative treatment strategy remains undetermined. This study evaluates the efficacy of different adjuvant treatments on disease-free survival (DFS) and overall survival (OS) in HCC patients with MVI following curative resection.

METHODS

A retrospective cohort of 409 HCC patients with MVI who underwent curative resection from three clinical centers between 2017 and 2024 was analyzed. Patients were stratified into three groups: TACE alone (n=132), TACE + targeted therapy (n=58), and TACE + targeted immunotherapy (n=68). Propensity score matching (PSM) was employed to balance confounding factors. Kaplan-Meier survival curves and Cox regression models were used to assess DFS and OS. A nomogram was constructed for individualized DFS prediction.

RESULTS

After PSM, both the TACE + targeted therapy and TACE + targeted immunotherapy groups exhibited significantly prolonged DFS compared to TACE alone (median DFS: 16 vs 22 and 21 months, respectively; p=0.027). No significant differences were observed in OS across the groups. The nomogram for DFS demonstrated robust predictive performance, with a C-index of 0.709 and 0.645 in the training and validation cohorts, respectively, supporting its utility in clinical decision-making.

CONCLUSION

In HCC patients with MVI, adjuvant TACE combined with targeted therapy or targeted immunotherapy significantly enhances DFS, though no OS benefit was observed. The developed nomogram provides a reliable tool for risk stratification and personalized postoperative management in this high-risk patient population.

摘要

背景

伴有微血管侵犯(MVI)的肝细胞癌(HCC)与高复发率及不良生存结局相关。尽管经动脉化疗栓塞术(TACE)、靶向治疗及免疫治疗等辅助治疗在改善结局方面显示出潜力,但最佳术后治疗策略仍未确定。本研究评估不同辅助治疗对MVI的HCC患者根治性切除术后无病生存期(DFS)和总生存期(OS)的疗效。

方法

分析了2017年至2024年间来自三个临床中心的409例接受根治性切除的MVI的HCC患者的回顾性队列。患者被分为三组:单纯TACE组(n = 132)、TACE + 靶向治疗组(n = 58)和TACE + 靶向免疫治疗组(n = 68)。采用倾向评分匹配(PSM)来平衡混杂因素。使用Kaplan-Meier生存曲线和Cox回归模型评估DFS和OS。构建列线图用于个体化DFS预测。

结果

PSM后,与单纯TACE组相比,TACE + 靶向治疗组和TACE + 靶向免疫治疗组的DFS均显著延长(中位DFS:分别为16个月与22个月和21个月;p = 0.027)。各组间OS未观察到显著差异。DFS列线图显示出强大的预测性能,训练队列和验证队列中的C指数分别为0.709和0.645,支持其在临床决策中的实用性。

结论

在MVI的HCC患者中,辅助TACE联合靶向治疗或靶向免疫治疗可显著提高DFS,尽管未观察到OS获益。所开发的列线图为这一高危患者群体的风险分层和个性化术后管理提供了可靠工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/98d47b9909af/JHC-12-561-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/e79ad3896c6c/JHC-12-561-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/39221d0ce8a9/JHC-12-561-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/8e16f71c0e17/JHC-12-561-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/e40ba9f4f143/JHC-12-561-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/7b3a05680f3a/JHC-12-561-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/481c7c16963f/JHC-12-561-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/98d47b9909af/JHC-12-561-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/e79ad3896c6c/JHC-12-561-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/39221d0ce8a9/JHC-12-561-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/8e16f71c0e17/JHC-12-561-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/e40ba9f4f143/JHC-12-561-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/7b3a05680f3a/JHC-12-561-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/481c7c16963f/JHC-12-561-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bad2/11930282/98d47b9909af/JHC-12-561-g0007.jpg

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