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Efficacy of Second-line Lenvatinib for Hepatocellular Carcinoma After Early Progression on Atezolizumab-Bevacizumab.

Anticancer research 2026 Vol.46(3) p. 1609-1618

Muto H, Kuzuya T, Tachi Y, Nagano Y, Kajino Y, Matsushita M, Hagihara S, Yamamoto S, Kobayashi T, Katano Y, Ohmiya N, Hashimoto S, Ariga M, Morisaki S, Komura G, Nakano T, Tanaka H, Nakaoka K, Ohno E, Funasaka K, Nagasaka M, Miyahara R, Hirooka Y

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[BACKGROUND/AIM] Atezolizumab plus bevacizumab (Ate+Bev) is widely used as first-line therapy for unresectable hepatocellular carcinoma (HCC).

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BibTeX ↓ RIS ↓
APA Muto H, Kuzuya T, et al. (2026). Efficacy of Second-line Lenvatinib for Hepatocellular Carcinoma After Early Progression on Atezolizumab-Bevacizumab.. Anticancer research, 46(3), 1609-1618. https://doi.org/10.21873/anticanres.18056
MLA Muto H, et al.. "Efficacy of Second-line Lenvatinib for Hepatocellular Carcinoma After Early Progression on Atezolizumab-Bevacizumab.." Anticancer research, vol. 46, no. 3, 2026, pp. 1609-1618.
PMID 41760254

Abstract

[BACKGROUND/AIM] Atezolizumab plus bevacizumab (Ate+Bev) is widely used as first-line therapy for unresectable hepatocellular carcinoma (HCC). However, a subset of patients experience early disease progression, often detected at the first radiologic assessment around 6 weeks. Evidence guiding second-line therapy in this subgroup is limited, and the clinical value of lenvatinib after early progressive disease (PD) remains unclear.

[PATIENTS AND METHODS] We retrospectively analyzed 36 patients with unresectable HCC who received lenvatinib after failure of first-line Ate+Bev. Patients were stratified by early PD, defined as radiologic progression at the scheduled 6-week assessment after starting Ate+Bev. Outcomes included antitumor response, progression-free survival (PFS), and overall survival (OS).

[RESULTS] Objective response rate (ORR) and disease control rate (DCR) assessed by RECIST 1.1 were comparable between patients with and without early PD (ORR: 28.6% . 13.8%; DCR: 85.7% . 86.2%; =0.342). Median PFS was also similar between groups [5.2 months (95% confidence interval=1.9-NA) . 6.1 months (3.7-7.5); =0.307]. In multivariate analyses adjusting for Child-Pugh class, Barcelona Clinic Liver Cancer (BCLC) stage, and reduced starting dose, early PD was not significantly associated with either PFS or OS, whereas Child-Pugh class A was independently associated with improved OS. Correlation between first- and second-line PFS was weak and non-significant (r=0.077, =0.682).

[CONCLUSION] Lenvatinib demonstrated comparable antitumor activity and survival outcomes even in patients with early PD on first-line Ate+Bev, indicating that early radiologic progression does not necessarily signify refractoriness to subsequent systemic therapy. These findings support lenvatinib as a viable second-line option regardless of early Ate+Bev response, particularly in patients with preserved liver function. Larger prospective studies are needed to confirm these observations.

MeSH Terms

Humans; Liver Neoplasms; Carcinoma, Hepatocellular; Quinolines; Female; Male; Phenylurea Compounds; Middle Aged; Aged; Antibodies, Monoclonal, Humanized; Disease Progression; Retrospective Studies; Bevacizumab; Antineoplastic Combined Chemotherapy Protocols; Adult; Treatment Outcome; Progression-Free Survival; Aged, 80 and over