Real-world treatment patterns and outcomes for patients with advanced hepatocellular carcinoma initially treated with PD-1 inhibitors

•Patient characteristics were associated with treatment patterns in HCC.•Tislelizumab, camrelizumab, and tislelizumab + TACE had similar effectiveness in advanced HCC.•PVTT was an independent risk factor for PFS in advanced HCC patients. Programmed cell death protein-1 (PD-1) inhibitors have shown p...

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Veröffentlicht in:International immunopharmacology 2024-05, Vol.132, p.111947-111947, Article 111947
Hauptverfasser: Zou, Huimin, Ge, Ying, Chen, Wenge, Yao, Dongning, Oi Lam Ung, Carolina, Lai, Yunfeng, Hu, Hao
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Sprache:eng
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Zusammenfassung:•Patient characteristics were associated with treatment patterns in HCC.•Tislelizumab, camrelizumab, and tislelizumab + TACE had similar effectiveness in advanced HCC.•PVTT was an independent risk factor for PFS in advanced HCC patients. Programmed cell death protein-1 (PD-1) inhibitors have shown promising clinical efficacy in treating advanced hepatocellular carcinoma (HCC). However, little evidence exists regarding their treatment patterns and outcomes in real-world practice in China. This study aimed to investigate real-world treatment patterns and outcomes of PD-1 inhibitors as first-line therapies for patients with advanced HCC in China. The study population included adult patients with advanced HCC who were initially treated with PD-1 inhibitors from April 2020 to November 2022 in China. Descriptive statistics were used to report first-line treatment patterns and associations between patient characteristics and the most frequently used treatment patterns. The effectiveness of first-line treatment with PD-1 inhibitors was also evaluated according to survival and tumor response. The analyses enrolled 480 patients. The four most frequently used first-line treatment patterns of camrelizumab, tislelizumab, camrelizumab + TACE, and tislelizumab + TACE showed statistical differences in patient characteristics of gender, HBV infection, liver cirrhosis, BCLC stage, and portal vein tumor thrombus (all P 
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2024.111947