Mahn, Robert; Glüer, Oscar André; Sadeghlar, Farsaneh; Möhring, Christian; Zhou, Taotao; Anhalt, Thomas; Monin, Malte Benedikt; Kania, Alexander; Glowka, Tim R.; Feldmann, Georg; Brossart, Peter; Kalff, Joerg C.; Schmidt-Wolf, Ingo G. H.; Strassburg, Christian P.; Gonzalez-Carmona, Maria A.: First-Line Treatment for Advanced Hepatocellular Carcinoma : A Three-Armed Real-World Comparison. In: Journal of hepatocellular carcinoma. 2024, vol. 11, 81-94.
Online-Ausgabe in bonndoc: https://hdl.handle.net/20.500.11811/13562
@article{handle:20.500.11811/13562,
author = {{Robert Mahn} and {Oscar André Glüer} and {Farsaneh Sadeghlar} and {Christian Möhring} and {Taotao Zhou} and {Thomas Anhalt} and {Malte Benedikt Monin} and {Alexander Kania} and {Tim R. Glowka} and {Georg Feldmann} and {Peter Brossart} and {Joerg C. Kalff} and {Ingo G. H. Schmidt-Wolf} and {Christian P. Strassburg} and {Maria A. Gonzalez-Carmona}},
title = {First-Line Treatment for Advanced Hepatocellular Carcinoma : A Three-Armed Real-World Comparison},
publisher = {Dove Medical Press},
year = 2024,
month = jan,

journal = {Journal of hepatocellular carcinoma},
volume = 2024, vol. 11,
pages = 81--94,
note = {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.},

url = {https://hdl.handle.net/20.500.11811/13562}
}

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