Application and Resistance Mechanisms of Lenvatinib in Patients with Advanced Hepatocellular Carcinoma
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Lenvatinib, a multitargeted tyrosine kinase inhibitor (TKI), is one of the preferred targeted drugs for the treatment of advanced hepatocellular carcinoma (aHCC). Since the REFLECT study showed that lenvatinib was noninferior to sorafenib in overall survival (OS), lenvatinib monotherapy has been widely used for aHCC. Moreover, lenvatinib combination therapy, especially lenvatinib combined with immune checkpoint inhibitors (ICIs), has shown more encouraging clinical results. However, drug development and comprehensive treatment have not significantly improved the prognosis, and lenvatinib resistance is often encountered in treatment. The underlying molecular mechanism of lenvatinib resistance is still unclear, and studies to solve drug resistance are ongoing. The molecular mechanisms of lenvatinib resistance in patients with aHCC include the regulation of signaling pathways, the regulation of noncoding RNAs, the impact of the immune microenvironment, tumor stem cell activation and other mechanisms. This review aims to (1) summarize the progress of lenvatinib in treating aHCC, (2) delineate the known lenvatinib resistance mechanisms of current therapy, and (3) describe the development of therapeutic methods intended to overcome these resistance mechanisms.
Mesenchymal Stem Cell-Derived Exosomes in Cancer Resistance Against Therapeutics.
Easwaran V, Pai K, Pai K Cancers (Basel). 2025; 17(5).
PMID: 40075675 PMC: 11898417. DOI: 10.3390/cancers17050831.
Chen Z, Ou L, Ma L Mol Cell Biochem. 2025; .
PMID: 40025300 DOI: 10.1007/s11010-025-05218-x.
Ma Y, Duan S, Ren S, Bu D, Li Y, Cai X Front Med (Lausanne). 2024; 11:1483291.
PMID: 39624043 PMC: 11609927. DOI: 10.3389/fmed.2024.1483291.
Esmael N, Lubin I, Tur-Kaspa R, Zemel R Cancers (Basel). 2024; 16(22).
PMID: 39594719 PMC: 11592932. DOI: 10.3390/cancers16223763.
Tang S, Gao Y, Yan X, Zhi W, Han Y Front Oncol. 2024; 14:1431069.
PMID: 39035736 PMC: 11257876. DOI: 10.3389/fonc.2024.1431069.