Real-World Efficacy and Safety of Lenvatinib in Korean Patients with Advanced Hepatocellular Carcinoma: A Multicenter Retrospective Analysis

被引:47
|
作者
Cheon, Jaekyung [1 ]
Chon, Hong Jae [2 ]
Bang, Yeonghak [3 ]
Park, Neung Hwa [1 ]
Shin, Jung Woo [1 ]
Kim, Kang Mo [4 ]
Lee, Han Chu [4 ]
Lee, Jooho [5 ,6 ]
Yoo, Changhoon [3 ]
Ryoo, Baek-Yeol [3 ]
机构
[1] Univ Ulsan, Ulsan Univ Hosp, Dept Internal Med, Coll Med, Ulsan, South Korea
[2] CHA Univ, CHA Bundang Med Ctr, Sch Med, Dept Med Oncol, Seongnam, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Gastroenterol, Seoul, South Korea
[5] CHA Univ, Sch Med, CHA Bundang Med Ctr, Dept Gastroenterol, Seongnam, South Korea
[6] CHA Univ, Sch Med, CHA Bundang Med Ctr, Dept Hepatol, Seongnam, South Korea
关键词
Lenvatinib; Hepatocellular carcinoma; Liver cancer; Real-world conditions; SORAFENIB; THERAPY;
D O I
10.1159/000508901
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction/Objective: Lenvatinib demonstrated efficacy and safety in patients with advanced hepatocellular carcinoma (HCC) in the randomized phase III REFLECT trial. Considering the discrepancies in patients between clinical trial data and daily practice, an account of practical experience is needed. Methods: We conducted a multicenter retrospective analysis in which 3 tertiary referral centers participated. A total of 92 patients with advanced HCC treated with lenvatinib between September 2018 and January 2020 were analyzed. Results: Lenvatinib was used as the first-line therapy for 67 (72.8%) patients, and for 25 (27.2%) patients previously treated with other systemic therapy including immune checkpoint inhibitors. At the time of initiation of lenvatinib, 74 (80.4%) and 18 (19.6%) patients were classified as Child-Pugh A and B, respectively. Thirty-five patients (38.0%) had extensive disease that would have excluded them from the REFLECT trial. In the Child-Pugh A group, the response rate graded according to the Response Evaluation Criteria in Solid Tumors v1.1 was 21.1%, median progression-free survival (PFS) was 4.6 (95% confidence interval [CI] 3.1-6.1) months, and overall survival (OS) was 10.7 (95% CI 4.8-16.5) months for patients treated with first-line lenvatinib (n= 57). With second- or later-line lenvatinib (n= 17), median PFS and OS were 4.1 (95% CI 3.1-5.1) and 6.4 (95% CI 5.1-7.7) months, respectively. In the Child-Pugh B group (n= 18), median PFS and OS were 2.6 (95% CI 0.6-4.6) and 5.3 (95% CI 2.0-8.5) months, respectively. The most common grade 3-4 toxicities were hyperbilirubinemia (n= 8; 8.7%), AST elevation (n= 6; 6.5%), and diarrhea (n= 5; 5.4%) across all study patients. Conclusions: In this real-world study, lenvatinib was found to be well tolerated and effective in more heterogeneous HCC patient populations. (c) 2020 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:613 / 624
页数:12
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