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Published in: Journal of Cancer Research and Clinical Oncology 17/2023

02-09-2023 | Lenvatinib | Review

Efficacy and safety of atezolizumab plus bevacizumab versus lenvatinib for unresectable hepatocellular carcinoma: a systematic review and meta-analysis

Authors: Junning Liu, Linfeng Yang, Song Wei, Jijiang Li, Pengsheng Yi

Published in: Journal of Cancer Research and Clinical Oncology | Issue 17/2023

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Abstract

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 (I2) = 0.0%, p = 0.590], compared with lenvatinib group but no significant difference in OS (HR 0.87, 95% CI 0.75–1.01; I2 = 0.0%, p = 0.597), objective response rate (ORR) [risk ratio (RR) 0.89, 95% CI 0.79–1.02; I2 = 19.3%, p = 0.283] and disease control rate (DCR) (RR 1.03, 95% CI 0.98–1.09; I2 = 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; I2 = 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; I2 = 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.
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Literature
go back to reference Kuzuya T, Ishigami M, Ito T, Ishizu Y, Honda T, Ishikawa T et al (2019) Clinical characteristics and outcomes of candidates for second-line therapy, including regorafenib and ramucirumab, for advanced hepatocellular carcinoma after sorafenib treatment. Hepatol Res 49(9):1054–1065. https://doi.org/10.1111/hepr.13358CrossRefPubMed Kuzuya T, Ishigami M, Ito T, Ishizu Y, Honda T, Ishikawa T et al (2019) Clinical characteristics and outcomes of candidates for second-line therapy, including regorafenib and ramucirumab, for advanced hepatocellular carcinoma after sorafenib treatment. Hepatol Res 49(9):1054–1065. https://​doi.​org/​10.​1111/​hepr.​13358CrossRefPubMed
go back to reference Sasaki R, Nagata K, Fukushima M, Haraguchi M, Miuma S, Miyaaki H et al (2022) Evaluating the role of hepatobiliary phase of gadoxetic acid-enhanced magnetic resonance imaging in predicting treatment impact of lenvatinib and atezolizumab plus bevacizumab on unresectable hepatocellular carcinoma. Cancers (basel). https://doi.org/10.3390/cancers14030827CrossRefPubMed Sasaki R, Nagata K, Fukushima M, Haraguchi M, Miuma S, Miyaaki H et al (2022) Evaluating the role of hepatobiliary phase of gadoxetic acid-enhanced magnetic resonance imaging in predicting treatment impact of lenvatinib and atezolizumab plus bevacizumab on unresectable hepatocellular carcinoma. Cancers (basel). https://​doi.​org/​10.​3390/​cancers14030827CrossRefPubMed
Metadata
Title
Efficacy and safety of atezolizumab plus bevacizumab versus lenvatinib for unresectable hepatocellular carcinoma: a systematic review and meta-analysis
Authors
Junning Liu
Linfeng Yang
Song Wei
Jijiang Li
Pengsheng Yi
Publication date
02-09-2023
Publisher
Springer Berlin Heidelberg
Published in
Journal of Cancer Research and Clinical Oncology / Issue 17/2023
Print ISSN: 0171-5216
Electronic ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-023-05342-5

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