[1]姜 楠,黄金涛,聂 宏,等.TACE联合靶向免疫药物治疗晚期肝细胞癌的有效性和安全性[J].介入放射学杂志,2023,32(05):441-445.
 JIANG Nan,HUANG Jintao,NIE Hong,et al.The efficacy and safety of transarterial chemoembolization combined with targeted drugs and immune drugs for advanced hepatocellular carcinoma [J].journal interventional radiology,2023,32(05):441-445.
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TACE联合靶向免疫药物治疗晚期肝细胞癌的有效性和安全性()

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《介入放射学杂志》[ISSN:1008-794X/CN:31-1796/R]

卷:
32
期数:
2023年05
页码:
441-445
栏目:
肿瘤介入
出版日期:
2023-05-30

文章信息/Info

Title:
The efficacy and safety of transarterial chemoembolization combined with targeted drugs and immune drugs for advanced hepatocellular carcinoma
作者:
姜 楠 黄金涛 聂 宏 李婉慈 仲斌演 张 帅 沈 健 王万胜 朱晓黎 倪才方
Author(s):
JIANG Nan HUANG Jintao NIE Hong LI Wanci ZHONG Binyan ZHANG Shuai SHEN Jian WANG Wansheng ZHU Xiaoli NI Caifang.
Department of Interventional Radiology, First Affiliated Hospital of Soochow University, Suzhou, Jiangsu Province 215006, China
关键词:
【关键词】 经动脉化疗栓塞术 靶向治疗 免疫治疗 晚期肝细胞癌
文献标志码:
A
摘要:
【摘要】 目的 探讨TACE联合靶向免疫药物治疗晚期肝细胞癌(HCC)的疗效和安全性。方法 回顾性分析2019年1月至2021年9月苏州大学附属第一医院收治的37例晚期HCC患者的临床资料。采用TACE联合靶向免疫药物治疗(联合组)16例,单纯靶向免疫治疗(单纯组)21例。Kaplan-Meier法绘制生存曲线,比较两组的中位无进展生存期(mPFS)、中位总生存期(mOS)。根据mRECIST标准进行疗效评估,比较两组的客观缓解率(ORR)、疾病控制率(DCR)。观察两组患者的不良反应发生情况。结果 联合组的mOS和mPFS分别为14.0个月(95% CI:4.59~23.41)和6.0个月(95% CI:4.04~7.96),单纯组分别为11.6个月(95% CI:4.53~18.67)和4.5个月(95% CI:3.38~6.63),差异有统计学意义(P=0.047、0.045)。联合组的ORR和DCR分别为68.75%和87.5%,较单纯组(4.76%和33.3%)均明显提高(P<0.01)。两组患者严重不良事件的发生差异无统计学意义(P=0.634)。结论 与单纯靶向免疫治疗相比,TACE联合靶向免疫药物治疗晚期HCC的疗效明显提高,且不会增加严重不良反应的发生。

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备注/Memo

备注/Memo:
(收稿日期:2022- 06- 18)
(本文编辑:新 宇)
更新日期/Last Update: 2023-05-30