Comparative Efficacy and Safety of Atezolizumab and Bevacizumab Between Hepatocellular Carcinoma Patients with Viral and Non-viral Infection: A Japanese Multicenter Observational Study
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Aim: This study compared the efficacy and safety of atezolizumab and bevacizumab (Atez/Bev) in patients with viral and non-viral infection in clinical settings.
Methods: We conducted the retrospective cohort study of 323 BCLC stage B or C hepatocellular carcinoma (HCC) patients with Child-Pugh class A, and a performance status of 0 or 1 who started Atez/Bev from September 2020 to December 2021 at 22 institutions in Japan. Patients with viral infection was defined as those who were either serum anti-HCV- Ab or HBs-Ag-positive, while patients with non-viral infection was defined as those who were both serum anti-HCV Ab- and HBs-Ag-negative. We constructed a propensity-score-matched cohort to minimize the risk of observable potential confounders.
Results: Propensity score matching produced 126 matched pairs for patients with viral versus non-viral infection. After matching, the significant differences in baseline demographic features did not exist between the two groups. The objective response rate was 20.6% and 24.6% in viral- and non-viral-related HCC patients, respectively, without a significant difference (p = 0.55). The disease control rate was not also significantly different (68.3% vs 69.0%, p = 1.00). The median progression-free survival was 7.0 months (95% confidence interval [CI] 6.0-9.6) and 6.2 months (95% CI 5.1-7.8) in patients with viral and non-viral infection, and the 12-month survival rates were 65.5% (95% CI 50.8-76.8) and 71.7% (95% CI 57.3-81.9) in those with viral and non-viral infection, respectively, which were not significantly different (p = 0.33, p = 0.38). No significant difference in treatment-related adverse events was found between the two groups.
Conclusions: Our etiology-based study demonstrated that Atez/Bev showed good efficacy and safety for HCC patient with non-viral infection as well as those with viral infection.
Shimose S, Saeki I, Ito T, Takeuchi Y, Tani J, Tomonari T Hepatol Int. 2025; .
PMID: 40019708 DOI: 10.1007/s12072-025-10781-y.
Wu Y, Cappuyns S, Loh A, Sun S, Lewis S, Sung M BJC Rep. 2024; 2(1):8.
PMID: 39516245 PMC: 11523972. DOI: 10.1038/s44276-024-00038-w.
Yim S, Lee S, Baek S, Sohn B, Jeong Y, Kang S Clin Mol Hepatol. 2024; 30(4):807-823.
PMID: 39038962 PMC: 11540371. DOI: 10.3350/cmh.2024.0333.
Kuwano A, Yada M, Tanaka K, Koga Y, Nagasawa S, Masumoto A Cancer Diagn Progn. 2024; 4(1):34-41.
PMID: 38173658 PMC: 10758843. DOI: 10.21873/cdp.10282.
Tanaka K, Tsuji K, Hiraoka A, Tada T, Hirooka M, Kariyama K Cancers (Basel). 2023; 15(17).
PMID: 37686624 PMC: 10486534. DOI: 10.3390/cancers15174348.