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Copyright ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Oncol. Oct 15, 2019; 11(10): 788-803
Published online Oct 15, 2019. doi: 10.4251/wjgo.v11.i10.788
Targeted agents for second-line treatment of advanced hepatocellular carcinoma
Nicola Personeni, Tiziana Pressiani, Silvia Bozzarelli, Lorenza Rimassa
Nicola Personeni, Tiziana Pressiani, Silvia Bozzarelli, Lorenza Rimassa, Medical Oncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center, IRCCS, Rozzano 20089, Milan, Italy
Nicola Personeni, Lorenza Rimassa, Department of Biomedical Sciences, Humanitas University, Pieve Emanuele 20090, Milan, Italy
Author contributions: Personeni N, Pressiani T, Bozzarelli S and Rimassa L performed data research; Personeni N, Pressiani T, Bozzarelli S and Rimassa L wrote the paper; Personeni N performed the critical revision of the manuscript.
Conflict-of-interest statement: Personeni N has received lecture fees from AbbVie and Gilead, and travel expenses from ArQule. Rimassa L has received consulting fees from Lilly, Bayer, Sirtex Medical, ArQule, Exelixis, Ipsen, Celgene, Eisai, and Roche, lecture fees from AstraZeneca, AbbVie, and Gilead, and travel expenses from ArQule and Ipsen. Pressiani T and Bozzarelli S have declared no conflict of interests. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. No writing assistance was utilized in the production of this manuscript.
Corresponding author: Lorenza Rimassa, MD, Associate Professor, Medical Oncology and Hematology Unit, Humanitas Cancer Center, Humanitas Clinical and Research Center, IRCCS, via Manzoni 56, Rozzano 20089, Department of Biomedical Sciences, Humanitas University, Pieve Emanuele 20090, Milan, Italy. lorenza.rimassa@hunimed.eu
Telephone: +39-2-82244573 Fax: +39-2-82244590
Received: April 29, 2019
Peer-review started: May 9, 2019
First decision: June 4, 2019
Revised: July 25, 2019
Accepted: August 27, 2019
Article in press: August 28, 2019
Published online: October 15, 2019
Processing time: 171 Days and 3.2 Hours
Abstract

Over the past ten years, sorafenib, a multikinase inhibitor, has been the standard of care for patients with unresectable hepatocellular carcinoma (HCC) and well-preserved liver function. Recently, lenvatinib, a different multikinase inhibitor, was shown to be non-inferior to sorafenib, in terms of survival, while all other agents previously tested failed to prove non-inferiority (or superiority) when compared to sorafenib. Similarly, in the second-line setting, most investigational drugs failed to provide better survival outcomes than placebo. However, in the last 2 years three positive phase III trials have been published in this setting. The RESORCE trial, a phase III study evaluating regorafenib in HCC patients who experienced disease progression after first-line treatment with sorafenib, showed better outcomes with regorafenib compared to placebo. More recently, the phase III CELESTIAL trial demonstrated the superiority of cabozantinib, a multikinase inhibitor targeting vascular endothelial growth factor receptor, MET, and AXL, vs placebo in the second- and third-line setting in patients progressing on or intolerant to sorafenib. The survival benefits of a sustained anti-angiogenic inhibition were demonstrated also with ramucirumab in the phase III REACH-2 trial in patients previously treated with sorafenib and who had high baseline alpha-fetoprotein levels. Overall, the adverse events reported in these trials were in line with the known safety profiles of the tested agents. After nearly a decade of a certain degree of stagnation, we are now witnessing a period of novel therapeutic advances with multikinase inhibitors and monoclonal antibodies that will likely change the treatment scenario of HCC.

Keywords: Hepatocellular carcinoma; Advanced-metastatic; Second-line; Third-line; Regorafenib; Cabozantinib; Ramucirumab; Angiogenesis; Multikinase inhibitor; MET; AXL; Vascular endothelial growth factor receptor 2

Core tip: During the last decade, sorafenib, a multikinase inhibitor, has emerged as the only systemic agent available for the treatment of patients with unresectable hepatocellular carcinoma. However, in recent years, lenvatinib, which is a different multikinase inhibitor, was shown to be non-inferior compared to sorafenib. Despite several negative phase III trials, novel drugs with similar, but not overlapping, properties have been recently shown to improve patient outcomes, thereby confirming the role of sustained anti-angiogenic inhibition in further lines of treatment. Here, we will discuss the results of the positive phase III trials of regorafenib, cabozantinib, and ramucirumab in patients failing sorafenib.