Transarterial Chemoembolization Plus Camrelizumab and Rivoceranib versus Camrelizumab and Rivoceranib Alone for BCLC Stage C Hepatocellular Carcinoma

被引:0
|
作者
Zhou, Wen-Jie [1 ,2 ]
Huang, Jin-Tao [1 ]
Lu, Xin [3 ]
Hu, Di [1 ]
Hong, Xin [4 ]
Wang, Fu-An [2 ]
Lv, Peng-Hua [2 ]
Zhu, Xiao-Li [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Dept Intervent Radiol, 188 Shizi St, Suzhou 215006, Peoples R China
[2] Yangzhou Univ, Northern Jiangsu Peoples Hosp, Clin Med Coll, Dept Intervent Radiol, Yangzhou, Peoples R China
[3] Xuzhou Cent Hosp, Dept Radiol, Xuzhou, Peoples R China
[4] Nantong Univ, Affiliated Hosp 2, Dept Intervent Radiol, Nantong, Peoples R China
关键词
hepatocellular carcinoma; camrelizumab; rivoceranib; TACE; survival; COMBINATION; TACE;
D O I
10.2147/JHC.S494520
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Camrelizumab and rivoceranib together provide a new first-line treatment approach for unresectable hepatocellular carcinoma (HCC). Meanwhile, transarterial chemoembolization (TACE) is an effective method for the local control of the HCC. The study compared the clinical benefit and safety between TACE with camrelizumab-rivoceranib and camrelizumab-rivoceranib Patients and Methods: This multi-center retrospective analysis included continuous BCLC-C HCC patients who received camrelizumab-rivoceranib with TACE and camrelizumab-rivoceranib alone from January 2020 to December 2022. The therapeutic response, progression-free survival (PFS), safety, and overall survival (OS) were compared. The quantitative data were compared via the t-test or Mann-Whitney U-test. Comparison of the categorical data was done by chi-square or Fisher's exact tests. The comparison of PFS with OS was compared by Log rank test. A Multivariate Cox regression test was utilized to identify risk variables for both PFS and OS. Results: This analysis comprised 132 BCLC-C HCC patients who received camrelizumab-rivoceranib alone (n = 74) or combined treatment (n = 58). The combined group displayed higher partial response (44.8% vs 21.6%, p = 0.004) and total response (55.2% versus 36.5%, p = 0.032) rates than camrelizumab-rivoceranib alone group. The median PFS (13.5 months vs 10.3 months, p = 0.046) and OS (22.8 months vs 18.4 months, p = 0.041) for the combined group was significantly longer relative to the camrelizumabrivoceranib alone group. Additional risk factors, excluding the therapy option, were a higher alpha-fetoprotein level and Eastern Cooperative Oncology Group performance status. The incident rates of camrelizumab-rivoceranib-related advents were comparable between combined and camrelizumab-rivoceranib alone groups (46.3% vs 51.4%, p = 0.572). The combined group contained 33 Conclusion: For BCLC-C HCC patients, TACE may significantly increase the therapeutic effectiveness of camrelizumab-rivoceranib without increasing the risk of camrelizumab-rivoceranib-related complications.
引用
收藏
页码:2515 / 2524
页数:10
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