PMID- 37658861 OWN - NLM STAT- MEDLINE DCOM- 20231102 LR - 20231102 IS - 1432-1335 (Electronic) IS - 0171-5216 (Linking) VI - 149 IP - 17 DP - 2023 Nov TI - Efficacy and safety of atezolizumab plus bevacizumab versus lenvatinib for unresectable hepatocellular carcinoma: a systematic review and meta-analysis. PG - 16191-16201 LID - 10.1007/s00432-023-05342-5 [doi] AB - BACKGROUND: Atezolizumab plus bevacizumab and lenvatinib are the current first-line systematic therapy for unresectable hepatocellular carcinoma (uHCC). However, the selection of initial treatment among the two therapies are controversial. This meta-analysis aims to compare efficacy and safety between atezolizumab plus bevacizumab and lenvatinib. METHODS: We systematically searched for studies on atezolizumab plus bevacizumab and lenvatinib in the online databases PubMed, Embase, Web of Science and Cochrane Library. The outcome data including overall survival (OS), progression free survival (PFS), tumor response and adverse events (AEs), were independently extracted by two authors in a standardized way. RESULTS: Eight retrospective cohort studies with 3690 patients (atezolizumab plus bevacizumab: 1680, lenvatinib: 2010) were included in the meta-analysis. The atezolizumab plus bevacizumab group had significant longer PFS [hazard ratio (HR) 0.76, 95% confidence intervals (CI) 0.65-0.88; I squared statistic (I(2)) = 0.0%, p = 0.590], compared with lenvatinib group but no significant difference in OS (HR 0.87, 95% CI 0.75-1.01; I(2) = 0.0%, p = 0.597), objective response rate (ORR) [risk ratio (RR) 0.89, 95% CI 0.79-1.02; I(2) = 19.3%, p = 0.283] and disease control rate (DCR) (RR 1.03, 95% CI 0.98-1.09; I(2) = 0.0%, p = 0.467) among them. Moreover, patients receiving atezolizumab plus bevacizumab exhibited lower incidences of grade 3/4 AEs than those receiving lenvatinib (RR 0.65, 95% CI 0.51-0.83; I(2) = 69.3%, p = 0.003). However, in non-viral patients group, lenvatinib delivered favorable outcomes in OS (HR 1.32, 95% CI 1.04-1.67; I(2) = 0.0%, p = 0.380) compared with atezolizumab plus bevacizumab. CONCLUSION: Atezolizumab plus bevacizumab provides potential advantage in efficacy and better safety than lenvatinib in the treatment of uHCC. Lenvatinib is an appropriate effective alternative to atezolizumab plus bevacizumab in patients without viral infecting. CI - (c) 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. FAU - Liu, Junning AU - Liu J AD - Department of Hepato-Biliary-Pancrease II, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, China. FAU - Yang, Linfeng AU - Yang L AD - Department of Hepato-Biliary-Pancrease II, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, China. FAU - Wei, Song AU - Wei S AD - Department of Hepato-Biliary-Pancrease II, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, China. FAU - Li, Jijiang AU - Li J AD - Department of Hepato-Biliary-Pancrease II, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, China. FAU - Yi, Pengsheng AU - Yi P AD - Department of Hepato-Biliary-Pancrease II, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, China. liujunning98@163.com. LA - eng GR - 22SXQT0052/Bureau of Science and Technology Nanchong City/ PT - Journal Article PT - Meta-Analysis PT - Review PT - Systematic Review DEP - 20230902 PL - Germany TA - J Cancer Res Clin Oncol JT - Journal of cancer research and clinical oncology JID - 7902060 RN - 52CMI0WC3Y (atezolizumab) RN - 2S9ZZM9Q9V (Bevacizumab) RN - EE083865G2 (lenvatinib) SB - IM MH - Humans MH - Bevacizumab/adverse effects MH - *Carcinoma, Hepatocellular/drug therapy MH - Retrospective Studies MH - *Liver Neoplasms/drug therapy OTO - NOTNLM OT - Atezolizumab OT - Bevacizumab OT - Hepatocellular carcinoma OT - Lenvatinib OT - Meta-analysis EDAT- 2023/09/04 01:22 MHDA- 2023/11/02 12:42 CRDT- 2023/09/02 11:03 PHST- 2023/07/30 00:00 [received] PHST- 2023/08/24 00:00 [accepted] PHST- 2023/11/02 12:42 [medline] PHST- 2023/09/04 01:22 [pubmed] PHST- 2023/09/02 11:03 [entrez] AID - 10.1007/s00432-023-05342-5 [pii] AID - 10.1007/s00432-023-05342-5 [doi] PST - ppublish SO - J Cancer Res Clin Oncol. 2023 Nov;149(17):16191-16201. doi: 10.1007/s00432-023-05342-5. Epub 2023 Sep 2.