Transarterial chemoembolization combined with sintilimab and lenvatinib for the treatment of unresectable hepatocellular carcinoma: a retrospective study

被引:2
|
作者
Shen, Chenyu [1 ,2 ,3 ]
Jiang, Wenxi [4 ]
Chen, Ruiqing [3 ]
Li, Lingbing [1 ,2 ,3 ]
Wu, Yunbo [4 ]
Tan, Long [4 ]
Chen, Yadong [4 ]
Zhang, Weiqiang [4 ]
Wang, Zhijun [1 ,2 ,3 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 2, Dept Geriatr Med, 28 Fuxing Rd, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 2, Natl Clin Res Ctr Geriatr Dis, 28 Fuxing Rd, Beijing 100853, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Intervent Radiol, Beijing 100853, Peoples R China
[4] Cent Comm Communist Party China, Hlth Serv Dept Guard Bur, Gen Off, 15 Wenjin St, Beijing 100017, Peoples R China
关键词
Unresectable hepatocellular carcinoma; TACE; Sintilimab; Lenvatinib; Combination therapy; TOLERANCE;
D O I
10.1007/s00432-024-05949-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThe treatment of unresectable hepatocellular carcinoma (uHCC) challenging due to unfulfilled clinical requirements.ObjectiveTo evaluate the safety and efficacy of combining transarterial chemoembolization (TACE) with sintilimab and lenvatinib in the treatment of uHCC.MethodsWe retrospectively analyzed the data of patients with uHCC who were treated with a combination of TACE, sintilimab, and lenvatinib between May 2019 and December 2021 at the Chinese PLA General Hospital. Systemic treatment was started 1 week after TACE was performed. Sintilimab was administered intravenously at a dosage of 200 mg every three weeks, and lenvatinib was given orally at dosages of 8 mg or 12 mg daily, contingent upon the weight of the patients. The primary endpoint was the objective response rate (ORR) as per the mRECIST. Secondary endpoints were disease control rate (DCR), progression-free survival (PFS), overall survival (OS) and treatment-related adverse events (tr-AEs).ResultsA total of 32 patients were enrolled in the study. Among them, 9 patients were classified as Barcelona Clinic Liver Cancer-B (BCLC-B), 23 patients were classified as BCLC-C, 14 patients diagnosed with portal vein tumors, and 12 patients were diagnosed with extra hepatic metastases. The ORR and DCR were 75% and 90.6% respectively, with 4 patients exhibiting (12.5%) complete response, 20 patients exhibiting (62.5%) partial response, 5 patients exhibiting (15.6%) stable disease, and 3 patients exhibiting (9.4%) progressive disease. With a median follow-up time of 19.6 months, the median PFS was 9.9 months, and the median OS was 33.3 months. A total of 31 patients experienced different degrees of tr-AEs, of which 2 were grade 3 tr-AEs.ConclusionThe combination therapy of TACE, sintilimab, and lenvatinib demonstrates satisfactory efficacy in the treatment of uHCC with manageable tr-AEs.
引用
收藏
页数:8
相关论文
共 50 条
  • [1] Effectiveness of transarterial chemoembolization combined with lenvatinib plus sintilimab in unresectable hepatocellular carcinoma
    Cao, Fei
    Yang, Yi
    Si, Tongguo
    Luo, Jun
    Zeng, Hui
    Zhang, Zhewei
    Chen, Yi
    Zheng, Jiaping
    JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (04)
  • [2] Transarterial chemoembolization combined with lenvatinib versus transarterial chemoembolization combined with sorafenib for unresectable hepatocellular carcinoma: A comparative retrospective study
    Zhang, Jin-Xing
    Chen, Yu-Xing
    Zhou, Chun-Gao
    Liu, Jin
    Liu, Sheng
    Shi, Hai-Bin
    Zu, Qing-Quan
    HEPATOLOGY RESEARCH, 2022, 52 (09) : 794 - 803
  • [3] Lenvatinib in combination with transarterial chemoembolization for treatment of unresectable hepatocellular carcinoma (uHCC): a retrospective controlled study
    Fu, Zhigang
    Li, Xiaowei
    Zhong, Jiaming
    Chen, Xiaoxia
    Cao, Kunkun
    Ding, Ning
    Liu, Li
    Zhang, Xiaoli
    Zhai, Jian
    Qu, Zengqiang
    HEPATOLOGY INTERNATIONAL, 2021, 15 (03) : 663 - 675
  • [4] Lenvatinib in combination with transarterial chemoembolization for treatment of unresectable hepatocellular carcinoma (uHCC): a retrospective controlled study
    Zhigang Fu
    Xiaowei Li
    Jiaming Zhong
    Xiaoxia Chen
    Kunkun Cao
    Ning Ding
    Li Liu
    Xiaoli Zhang
    Jian Zhai
    Zengqiang Qu
    Hepatology International, 2021, 15 : 663 - 675
  • [5] Lenvatinib combined with sintilimab plus transarterial chemoembolization as first-line treatment for advanced hepatocellular carcinoma
    Sun, Sha-Sha
    Guo, Xiao-Di
    Li, Wen-Dong
    Chen, Jing-Long
    WORLD JOURNAL OF CLINICAL CASES, 2024, 12 (02)
  • [6] Transarterial chemoembolization combined with lenvatinib and sintilimab vs lenvatinib alone in intermediate-advanced hepatocellular carcinoma
    Wu, Fei-Da
    Zhou, Hai-Feng
    Yang, Wei
    Zhu, Di
    Wu, Bi-Fei
    Shi, Hai-Bin
    Liu, Sheng
    Zhou, Wei-Zhong
    WORLD JOURNAL OF GASTROINTESTINAL ONCOLOGY, 2025, 17 (01)
  • [7] Efficiency and Stability of Transarterial Chemoembolization Combined With or Without Lenvatinib for Unresectable Hepatocellular Carcinoma
    Zong, Zheng
    Tang, Rongyu
    Li, Mingyu
    Xiong, Xinmiao
    Li, Daixin
    Fan, Jing
    Ye, Wei
    Xue, Chenqi
    TURKISH JOURNAL OF GASTROENTEROLOGY, 2024, 35 (03): : 212 - 222
  • [8] Transarterial chemoembolization combined with lenvatinib plus tislelizumab for unresectable hepatocellular carcinoma: a multicenter cohort study
    Zhao, Yushan
    Wen, Shuwei
    Xue, Yaoqing
    Dang, Zhijun
    Nan, Zhiyu
    Wang, Dong
    Li, Xiao
    Feng, Duiping
    Chen, Yi
    FRONTIERS IN IMMUNOLOGY, 2024, 15
  • [9] Impact of combining Lenvatinib with Transarterial chemoembolization for unresectable hepatocellular carcinoma
    Long, Jianwu
    Liu, Longfei
    Yang, Xuefeng
    Lu, Xianzhou
    Qin, Lei
    PAKISTAN JOURNAL OF MEDICAL SCIENCES, 2023, 39 (06) : 1847 - 1852
  • [10] The Efficacy of TACE Combined With Lenvatinib Plus Sintilimab in Unresectable Hepatocellular Carcinoma: A Multicenter Retrospective Study
    Cao, Fei
    Yang, Yi
    Si, Tongguo
    Luo, Jun
    Zeng, Hui
    Zhang, Zhewei
    Feng, Duiping
    Chen, Yi
    Zheng, Jiaping
    FRONTIERS IN ONCOLOGY, 2021, 11