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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.
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页码:81 / 94
页数:14
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