肝脏 ›› 2026, Vol. 31 ›› Issue (6): 826-830.

• 肝肿瘤 • 上一篇    下一篇

特瑞普利单抗联合仑伐替尼在TACE治疗晚期肝癌中的应用效果

栾欣英, 赵金侠, 孙硕, 陈雨晨   

  1. 274200 菏泽 成武县人民医院药剂科(栾欣英,赵金侠,孙硕);
    102218 北京 北京清华长庚医院药学部药剂科(陈雨晨)
  • 收稿日期:2025-10-17 出版日期:2026-06-30 发布日期:2026-07-29

A study on the efficacy of toripalimab combined with lenvatinib in TACE treatment for advanced liver cancer

Luan Xinying1, Zhao Jinxia1, Sun Shuo1, Chen Yuchen2   

  1. 1. Department of Pharmacy, Chengwu County People′s Hospital, Heze 274200, China;
    2. Department of Pharmacy, Beijing Tsinghua Changgung Hospital, Beijing 102218, China
  • Received:2025-10-17 Online:2026-06-30 Published:2026-07-29

摘要: 目的 探讨特瑞普利单抗联合仑伐替尼在肝动脉化疗栓塞术(TACE)治疗晚期肝癌中的应用。方法 选取2020年9月至2024年9月菏泽市成武县人民医院收治的晚期肝癌患者150例,随机分为对照组(仑伐替尼+TACE)与观察组(在对照组基础上加用特瑞普利单抗),每组各75例。比较两组治疗效果及1年后的生存情况。结果 治疗后,观察组客观缓解率为58.67%(44/75),高于对照组的37.33%(28/75)(χ2=6.838,P=0.009)。观察组血管内皮生长因子、缺氧诱导因子-1α、成纤维细胞生长因子、甲胎蛋白、糖类抗原19-9、AST、ALT水平分别为(203.27±25.68)pg/mL、(30.86±4.59)ng/L、(20.42±2.97)pg/mL、(212.24±25.89)ng/mL、(49.26±9.37)U/mL、(51.28±9.85)U/L、(52.33±4.25)U/L,对照组分别为(228.15±22.17)pg/mL、(36.37±5.24)ng/L、(26.15±3.46)pg/mL、(271.61±23.47)ng/mL、(58.73±10.16)U/mL、(62.61±10.37)U/L、(59.74±5.69)U/L,两组比较差异均有统计学意义(P<0.05)。治疗后,两组不良反应发生率差异无统计学意义(P>0.05)。观察组1年存活率为58.67%(44/75),高于对照组的34.67%(26/75)(P<0.05)。结论 在TACE治疗晚期肝癌的基础上,联合应用特瑞普利单抗与仑伐替尼可显著提高客观缓解率,降低肿瘤标志物及血管生成相关因子水平,改善肝功能,且未增加不良反应发生率,有助于提高患者近期生存率。

关键词: 特瑞普利单抗, 仑伐替尼, 肝动脉化疗栓塞术, 晚期肝癌, 临床疗效

Abstract: Objective To investigate the efficacy of toripalimab combined with lenvatinib in the treatment of advanced liver cancer with transarterial chemoembolization (TACE). Methods A total of 150 patients with advanced liver cancer admitted to our hospital between September 2020 and September 2024 were enrolled. They were randomly assigned to the control group (lenvatinib plus TACE) and the observation group (lenvatinib + TACE combined with toripalimab), with 75 patients in each group. The therapeutic efficacy of the two groups was compared after treatment, and their survival status was followed up for 1 year. Results After treatment, the objective response rate (ORR) of the observation group reached 58.67%, which was notably higher compared to the 34.67% recorded in the control group (P<0.05). Regarding serum indicators, the observation group showed respective levels of vascular endothelial growth factor, hypoxia-inducible factor-1α, basic fibroblast growth factor, alpha-fetoprotein, carbohydrate antigen 19-9, aspartate aminotransferase, and alanine aminotransferase of (203.27±25.68) pg/mL, (30.86±4.59) ng/L, (20.42±2.97) pg/mL, (212.24±25.89) ng/mL, (49.26±9.37) U/mL, (51.28±9.85) U/L, and (52.33±4.25) U/L, respectively, which were significantly lower than those in the control group[(228.15±22.17) pg/mL, (36.37±5.24) ng/L, (26.15±3.46) pg/mL, (271.61±23.47) ng/mL, (58.73±10.16) U/mL, (62.61±10.37) U/L, (59.74±5.69) U/L], with statistical significance (P<0.05). The two groups had similar adverse reaction incidences (P>0.05). However, the observation group had a significantly higher 1-year survival rate (58.67%) than the control group (34.67%) (P<0.05). Conclusion The combination of toripalimab and lenvatinib with TACE in the treatment of advanced liver cancer can significantly improve the objective response rate, reduce tumor markers and angiogenesis-related factors, improve liver function, and increase prolong short-term survival without increasing the incidence of adverse reactions.

Key words: Toripalimab, Lenvatinib, Transarterial chemoembolization, Advanced liver cancer, Clinical efficacy