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HAIC + tislelizumab + lenvatinib

Development stage
Unknown
Lead developer
BeiGene
Modality
DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intra-arterial, Intravenous, Oral
01

Overview

This is a combination regimen consisting of hepatic arterial infusion chemotherapy (HAIC), the PD-1 inhibitor monoclonal antibody tislelizumab, and the multikinase inhibitor small molecule lenvatinib. HAIC delivers chemotherapeutic agents directly into the hepatic artery to target liver tumors. Tislelizumab is an immune checkpoint inhibitor that blocks programmed cell death protein 1 (PD-1) on T cells to enhance anti-tumor immunity. Lenvatinib inhibits multiple receptor tyrosine kinases involved in tumor angiogenesis and proliferation, including vascular endothelial growth factor receptors (VEGFRs), fibroblast growth factor receptors (FGFRs), platelet-derived growth factor receptor alpha (PDGFRα), RET proto-oncogene, and KIT proto-oncogene receptor tyrosine kinase. This triple combination has been investigated primarily for advanced or unresectable hepatocellular carcinoma (HCC), especially in patients with high tumor burden or portal vein tumor thrombosis. Clinical studies have shown improved overall survival and progression-free survival compared to dual regimens or monotherapy[1][2][4][5].

Other names
HAIC plus lenvatinib and tislelizumabHLP regimentriple combination therapy (HAIC, lenvatinib, tislelizumab)
02

Targets

FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDCD1 (Programmed cell death protein 1 receptor)FGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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