Abstract

Targeted therapies such as oral tyrosine kinase inhibitors (TKIs) are the main therapeutic strategy effective for advanced hepatocellular carcinoma (HCC). Currently six tyrosine kinase inhibitors for HCC therapy have been approved. The newly approved first-line drug donafenib represent the major milestones in HCC therapeutics in recent years. However, drug resistance in HCC remains challenging due to random mutations in target receptors as well as downstream pathways. TKIs-based combinatorial therapies with immune checkpoint inhibitors such as PD-1/PD-L1 antibodies afford a promising strategy to further clinical application. Recent developments of nanoparticle-based TKI delivery techniques improve drug absorption and bioavailability, enhance efficient targeting delivery, prolonged circulation time, and reduce harmful side effects on normal tissues, which may improve the therapeutic efficacy of the TKIs. In this review, we summarize the milestones and recent progress in clinical trials of TKIs for HCC therapy. We also provide an overview of the novel nanoparticle-based TKI delivery techniques that enable efficient therapy.

Highlights

  • According to GLOBOCAN 2020 statistics, estimated liver cancer summed up to 905,677 new cases and 830,180 deaths in 2020 worldwide [1]

  • Because multiple signaling pathways are involved in tumorigenesis and tumor progression, all tyrosine kinase inhibitor (TKI) for hepatocellular carcinoma (HCC) are multi-kinase inhibitors which are designed to target a wide range of targeted kinases

  • Combination strategies of TKIs plus immune checkpoint inhibitors appearing as a promising strategy to circumvent resistance mechanisms that can be encountered with TKIs, aiming at a synergistic antitumor effect

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Summary

INTRODUCTION

According to GLOBOCAN 2020 statistics, estimated liver cancer summed up to 905,677 new cases and 830,180 deaths in 2020 worldwide [1]. Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer. It occurs in approximately 85% of cirrhosis cases [2]. TKIs would inhibit activation of corresponding signaling pathways through binding irreversibly or reversibly to various sites during the initial activation of receptor tyrosine kinases (RTKs) [6]. This further prevents tumor growth and metastasis by preventing downstream signaling pathways from being activated [4, 7].

VEGFR-TKIs
PDGFR-TKIs
Other TKIs
COMPARISON OF DIFFERENT TKIS
NANOTECHNOLOGY AS THE POTENTIAL DELIVERY SYSTEM
MOLECULAR CLASSIFICATIONS OF HCC
BIOLOGICAL ALTERATIONS IN HCC GENESIS
Findings
CONCLUSION
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