Current status of first-line therapy, anti-angiogenic therapy and its combinations of other agents for unresectable hepatocellular carcinoma

被引:4
作者
Alqahtani, Saleh A. [1 ,2 ,3 ]
Colombo, Massimo G. [4 ]
机构
[1] Johns Hopkins Univ, Div Gastroenterol & Hepatol, Baltimore, MD 21287 USA
[2] King Faisal Specialist Hosp & Res Ctr, Liver Transplant Ctr, Riyadh 11564, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Biostat Epidemiol & Sci Comp Dept, Riyadh 11564, Saudi Arabia
[4] IRCCS San Raffaele Hosp, Liver Ctr, Via Olgettina 60, I-20132 Milan, Italy
关键词
Hepatocellular carcinoma; Immune checkpoint inhibitor; Lenvatinib; Multityrosine kinase inhibitor; Sorafenib; PHASE-III; DOUBLE-BLIND; SORAFENIB; LENVATINIB; SURVIVAL; IMPACT;
D O I
10.4251/wjgo.v13.i12.2038
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Globally, hepatocellular carcinoma (HCC) is a frequently diagnosed malignancy with rapidly increasing incidence and mortality rates. Unfortunately, many of these patients are diagnosed in the advanced stages when locoregional treatments are not appropriate. Before 2008, no effective drug treatments existed to prolong survival, until the breakthrough multi-tyrosine kinase inhibitor (TKI) sorafenib was developed. It remained the standard treatment option for advanced HCC for 10 years, with a battery of other candidate drugs in clinical trials failing to produce similar efficacy results. In 2018, the REFLECT trial introduced another multi-TKI, lenvatinib, which has non-inferior overall survival compared with sorafenib. Thus, offering patients and their treating physicians two effective treatment options. Recently, immunotherapy-based drugs, such as atezolizumab and bevacizumab, have shown promising results in patients with unresectable HCC. This review summarizes clinical trial and real-world data studies of sorafenib and lenvatinib in patients with unresectable HCC. We offer guidance on the optimal choice between the two treatments and discuss the potential of immunotherapy-based combination; when more data become available, this will likely make the choice between sorafenib and lenvatinib somewhat obsolete.
引用
收藏
页码:2038 / 2049
页数:12
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