Similar efficacy and safety between lenvatinib versus atezolizumab plus bevacizumab as the first-line treatment for unresectable hepatocellular carcinoma

被引:14
|
作者
Su, Chung-Wei [1 ,2 ]
Teng, Wei [1 ,2 ]
Lin, Po-Ting [1 ,2 ]
Jeng, Wen-Juei [1 ,2 ]
Chen, Kuei-An [3 ]
Hsieh, Yi-Chung [1 ,2 ]
Chen, Wei-Ting [1 ,2 ]
Ho, Ming-Mo [2 ,4 ]
Hsieh, Chia-Hsun [2 ,5 ]
Wang, Ching-Ting [2 ,6 ]
Chai, Pei-Mei [2 ,6 ]
Lin, Chen-Chun [1 ,2 ,7 ]
Lin, Chun-Yen [1 ,2 ,7 ]
Lin, Shi-Ming [1 ,2 ,7 ]
机构
[1] Chang Gung Mem Hosp, Linkou Med Ctr, Dept Gastroenterol & Hepatol, Taoyuan, Taiwan
[2] Chang Gung Univ, Coll Med, Taoyuan, Taiwan
[3] Chang Gung Mem Hosp, Linkou Med Ctr, Dept Med Imaging & Intervent, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp, Linkou Med Ctr, Dept Med Oncol, Taoyuan, Taiwan
[5] Tucheng Composite Municipal Hosp, Dept Med Oncol, New Taipei, Taiwan
[6] Chang Gung Mem Hosp, Linkou Med Ctr, Dept Nursing, Taoyuan, Taiwan
[7] Chang Gung Univ, Chang Gung Mem Hosp, Coll Med, Dept Gastroenterol & Hepatol,Linkou Branch, 199 Tung Hwa North Rd, Taipei 105, Taiwan
来源
CANCER MEDICINE | 2023年 / 12卷 / 06期
关键词
adverse event; atezolizumab plus bevacizumab; hepatocellular carcinoma; lenvatinib; survival; PHASE-III; HEPATITIS-B; SORAFENIB; THERAPY;
D O I
10.1002/cam4.5506
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundLenvatinib and atezolizumab plus bevacizumab(A + B) have been used for unresectable hepatocellular carcinoma (HCC) as first-line therapy. Real-world studies comparison of efficacy and safety in these two regimens are limited, we therefore conduct this study to investigate these issues. MethodsWe retrospectively reviewed patients received lenvatinib (n = 46) and A + B (n = 46) as first-line systemic therapy for unresectable HCC in a tertiary medical center. Objective response rate (ORR), progression free survival (PFS), and overall survival (OS) were evaluated according to modified Response Evaluation Criteria in Solid Tumors (mRECIST). Inverse probability weighting (IPW) was performed for baseline clinical features balance. ResultsA total of 92 patients with median age of 63.8 year-old, 78.3% male, 85.9% viral hepatitis infected, 67.4% BCLC stage C were enrolled. The median treatment and follow-up duration were 4.7 months and 9.4 months, respectively. There was no significant difference in ORR (26.1% vs. 41.3%, p = 0.1226), PFS (5.9 vs. 5.3 months, p = 0.4066), and OS (not reached vs. not reached, p = 0.7128) between the lenvatinib and A + B groups. After IPW, the results of survival and response rate were also compared. Subgroup analysis suggested that using lenvatinib was not inferior to A + B in regards of PFS, including those with elder, Child-Pugh class B, beyond up-to-seven, or portal vein invasion VP4 patients. Among the lenvatinib treated patients, multivariate analysis showed patients elder than 65-year-old was an independent predictor associated with shorter PFS (adjust HR: 2.085[0.914-4.753], p = 0.0213). The incidence rates of adverse events were similar between two groups (76 vs. 63%, p = 0.1740). Both of two regimens had similarly few impact on liver function by comparison of baseline, third month, and sixth month albumin-bilirubin index and Child-Pugh score. ConclusionsThe efficacy and safety of lenvatinib are similar to A + B as a first-line systemic therapy for unresectable HCC.
引用
收藏
页码:7077 / 7089
页数:13
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