TY - JOUR
T1 - Efficacy of Second-line Lenvatinib for Hepatocellular Carcinoma After Early Progression on Atezolizumab-Bevacizumab
AU - MUTO, HISANORI
AU - KUZUYA, TEIJI
AU - TACHI, YOSHIHIKO
AU - NAGANO, YOSUKE
AU - KAJINO, YUTARO
AU - MATSUSHITA, MISAE
AU - HAGIHARA, SEIYA
AU - YAMAMOTO, SATOSHI
AU - KOBAYASHI, TAKASHI
AU - KATANO, YOSHIAKI
AU - OHMIYA, NAOKI
AU - HASHIMOTO, SENJU
AU - ARIGA, MIZUKI
AU - MORISAKI, SAYAKA
AU - KOMURA, GAKUSHI
AU - NAKANO, TAKUJI
AU - TANAKA, HIROYUKI
AU - NAKAOKA, KAZUNORI
AU - OHNO, EIZABURO
AU - FUNASAKA, KOHEI
AU - NAGASAKA, MITSUO
AU - MIYAHARA, RYOJI
AU - HIROOKA, YOSHIKI
N1 - Publisher Copyright:
© 2025 xxxx
PY - 2026/3
Y1 - 2026/3
N2 - 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% vs. 13.8%; DCR: 85.7% vs. 86.2%; p=0.342). Median PFS was also similar between groups [5.2 months (95% confidence interval=1.9-NA) vs. 6.1 months (3.7-7.5); p=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, p=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.
AB - 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% vs. 13.8%; DCR: 85.7% vs. 86.2%; p=0.342). Median PFS was also similar between groups [5.2 months (95% confidence interval=1.9-NA) vs. 6.1 months (3.7-7.5); p=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, p=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.
KW - Atezolizumab plus bevacizumab
KW - early progression
KW - hepatocellular carcinoma
KW - immune checkpoint inhibitor
KW - lenvatinib
KW - overall survival
KW - real-world study
KW - second-line therapy
UR - https://www.scopus.com/pages/publications/105031707616
UR - https://www.scopus.com/pages/publications/105031707616#tab=citedBy
U2 - 10.21873/anticanres.18056
DO - 10.21873/anticanres.18056
M3 - Article
C2 - 41760254
AN - SCOPUS:105031707616
SN - 0250-7005
VL - 46
SP - 1609
EP - 1618
JO - Anticancer research
JF - Anticancer research
IS - 3
ER -