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岭南现代临床外科 ›› 2024, Vol. 24 ›› Issue (05): 284-290.DOI: 10.3969/j.issn.1009-976X.2024.05.003

• 论著与临床研究 • 上一篇    下一篇

HAIC联合仑伐替尼和PD-1抗体对比HAIC联合仑伐替尼转化治疗肝细胞癌的回顾性研究

黄东东1, 田丰2, 方郁晖2, 邱益霖2, 何坤1,2,*   

  1. 1.中山市人民医院普外一科,广东中山 528403;
    2.广东医科大学第一临床医学院,广东湛江 524000
  • 通讯作者: *何坤,Email:hekun80@126.com
  • 基金资助:
    中山市医学科研项目(20211A020295)

A retrospective study of HAIC in combination with lenvatinib and PD-1 antibody versus HAIC in combination with lenvatinib for the translational treatment of hepatocellular carcinoma

HUANG Dong-dong1, TIAN Feng2, FANG Yu-hui2, QIU Yi-lin2, HE Kun1,2   

  1. 1. Department of General Surgery, Zhongshan People's Hospital, Zhongshan, Guangdong 528403, China;
    2. The First Clinical Medical College of Guangdong Medical University, Zhanjiang, Guangdong 524000, China
  • Received:2024-09-10 Online:2024-10-20 Published:2025-01-06
  • Contact: HE Kun, hekun80@126.com

摘要: 目的 回顾性分析65例中晚期肝细胞癌患者分别使用HAIC联合仑伐替尼和PD-1抗体与HAIC联合仑伐替尼转化切除的疗效及预后。方法 回顾性收集中山市人民医院自2020年3月至2023年3月期间获得成功转化切除的65例肝细胞癌患者,根据治疗方案不同分为联合组(HAIC联合仑伐替尼和PD-1抗体)和对照组(HAIC联合仑伐替尼),对两组患者的总生存期(OS)、无疾病进展生存期(PFS)、治疗相关的不良反应进行统计分析。结果 65例肝细胞癌患者根据 RECIST 1.1和mRECIST标准分别评估治疗,mRECIST标准,联合组PR 29例(74.4%),ORR 35例(89.7%),DCR 37例(94.9%);对照组,PR 9例(74.4%),ORR 17例(65.4%),DCR 24例(92.3%);总体中位生存时间约36个月,总体中位无复发生存期约28个月。其中联合组患者的中位生存时间为40个月,中位无复发生存期为32个月。对照组患者的中位生存时间为29个月、中位无复发生存期为25个月。联合组的PR、ORR、PR、OS、RFS均明显高于对照组(P<0.005)。结论 HAIC联合仑伐替尼和PD-1抗体可为中晚期HCC患者带来更显著的生存优势,有效延长其生存期,改善其生存质量。

关键词: 肝细胞癌, 肝动脉灌注化疗, FOLFOX方案, 联合治疗

Abstract: Objective To retrospectively analyze the efficacy and prognosis of HAIC combined with lenvatinib and PD-1 antibody in the treatment of hepatocellular carcinoma in patients with intermediate and advanced hepatocellular carcinoma in our center. Methods Sixty-five patients admitted to Zhongshan People′s Hospital from March 2020 to March 2023 were retrospectively collected and divided into a combination group (HAIC combined with lenvatinib and PD-1 antibody) and a control group (HAIC combined with lenvatinib) according to the different treatment regimens, and the overall survival (OS), disease progression-free survival (PFS), and treatment-related adverse effects of the patients in the two groups were statistically analyzed. Results Sixty-five patients with hepatocellular carcinoma were evaluated for treatment according to RECIST 1.1 and mRECIST criteria, respectively, According to the mRECIST criteria, there were 29 cases (74.4%) of PR, 35 cases (89.7%) of ORR, and 37 cases (94.9%) of DCR in the combined group; In the control group, there were 9 cases of PR (74.4%), 17 cases of ORR (65.4%), and 24 cases of DCR (92.3%); the overall median survival time was about 36 months, and the overall median relapse-free survival was about 28 months. The median survival time for patients in the combination group was 40 months, and the median relapse-free survival was 32 months. Patients in the control group had a median survival time of 29 months and a median relapse-free survival of 25 months. The PR, ORR, OS and RFS of the combination group were significantly higher than those of the control group, which were statistically different. Conclusion HAIC combined with lenvatinib and PD-1 antibody can bring more significant survival advantages for patients with intermediate and advanced HCC, effectively prolonging the survival of intermediate and advanced patients and improving the quality of patients′ survival.

Key words: hepatocellular carcinoma, hepatic artery perfusion chemotherapy, FOLFOX regimen, combination therapy

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