First-Line Treatment for Advanced Hepatocellular Carcinoma: A Three-Armed Real-World Comparison

被引:1
作者
Mahn, Robert [1 ]
Glueer, Oscar Andre [1 ]
Sadeghlar, Farsaneh [1 ]
Moehring, Christian [1 ]
Zhou, Taotao [1 ]
Anhalt, Thomas [1 ]
Monin, Malte Benedikt [1 ]
Kania, Alexander [2 ]
Glowka, Tim R. [2 ]
Feldmann, Georg [3 ]
Brossart, Peter [3 ]
Kalff, Joerg C. [2 ]
Schmidt-Wolf, Ingo G. H. [4 ]
Strassburg, Christian P. [1 ]
Gonzalez-Carmona, Maria A. [1 ,5 ]
机构
[1] Univ Hosp Bonn, Dept Internal Med 1, Bonn, Germany
[2] Univ Hosp Bonn, Dept Surg, Bonn, Germany
[3] Univ Hosp Bonn, Dept Internal Med 3, Bonn, Germany
[4] Univ Hosp Bonn, Dept Integrated Oncol CIO Bonn, Bonn, Germany
[5] Univ Hosp Bonn, Dept Internal Med 1, Venusberg Campus 1, D-53127 Bonn, Germany
关键词
HCC; first-line therapy; subgroups; ATEZOLIZUMAB PLUS BEVACIZUMAB; SORAFENIB;
D O I
10.2147/JHC.S432948
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Aim: There are several existing systemic 1st- line therapies for advanced hepatocellular carcinoma (HCC), including atezolizumab/bevacizumab (Atez/Bev), sorafenib and lenvatinib. This study aims to compare the effectiveness of these three 1st-line systemic treatments in a real-world setting for HCC, focusing on specific patient subgroups analysis.Methods: A total of 177 patients with advanced HCC treated with Atez/Bev (n = 38), lenvatinib (n = 21) or sorafenib (n = 118) as 1st line systemic therapy were retrospectively analyzed and compared. Primary endpoints included objective response rate (ORR), progression-free survival (PFS) and 15-month overall survival (15-mo OS). Subgroups regarding liver function, etiology, previous therapy and toxicity were analyzed.Results: Atez/Bev demonstrated significantly longer median 15-month OS with 15.03 months compared to sorafenib with 9.43 months (p = 0.04) and lenvatinib with 8.93 months (p = 0.05). Similarly, it had highest ORR of 31.6% and longest median PFS with 7.97 months, independent of etiology. However, significantly superiority was observed only compared to sorafenib (ORR: 4.2% (p < 0.001); PFS: 4.57 months (p = 0.03)), but not comparing to lenvatinib (ORR: 28.6% (p = 0.87); PFS: 3.77 months (p = 0.10)). Atez/ Bev also resulted in the longest PFS in patients with Child-Pugh A and ALBI 1 score and interestingly in those previously treated with SIRT. Contrary, sorafenib was non inferior in patients with impaired liver function.Conclusion: Atez/Bev achieved longest median PFS and 15-mo OS independent of etiology and particularly in patients with stable liver function or prior SIRT treatment. Regarding therapy response lenvatinib was non-inferior to Atez/Bev. Finally, sorafenib seemed to perform best for patients with deteriorated liver function.
引用
收藏
页码:81 / 94
页数:14
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