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. 2022 Oct 22;17(6):643–653. doi: 10.1007/s11523-022-00921-x

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© The Author(s) 2022

Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 1 — Study design. A total of 810 patients with HCC treated with ATEZO/BEVA or LEN as the first-line systemic treatment were evaluated. In the course of the study, 81 patients were excluded, resulting in 729 patients with HCC being included. Propensity score matching was then performed on the data of the 729 patients with HCC, resulting in 304 patients with HCC being included in the evaluation. HCC hepatocellular carcinoma, ATEZO/BEVA atezolizumab plus bevacizumab, ALBI albumin–bilirubin