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D-TACE + lenvatinib + tislelizumab

Development stage
Unknown
Lead developer
Wen Li
Modality
Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics, Device-based Delivery → Drug Delivery Systems
Administration
Intra-arterial, Oral, Intravenous
01

Overview

D-TACE + lenvatinib + tislelizumab is an investigational combination regimen being evaluated for the treatment of advanced unresectable hepatocellular carcinoma (HCC). The regimen integrates three distinct therapeutic modalities: Drug-eluting Bead Transarterial Chemoembolization (D-TACE) using pirarubicin-loaded CalliSpheres (100-300 µm), the oral multi-kinase inhibitor lenvatinib, and the intravenous anti-PD-1 monoclonal antibody tislelizumab. D-TACE provides a dual effect by delivering high-dose chemotherapy (pirarubicin) directly to the tumor while simultaneously inducing ischemia through embolization. Lenvatinib targets multiple tyrosine kinases, including VEGFR1-3 and FGFR1-4, to inhibit angiogenesis and lymphangiogenesis. Tislelizumab is a humanized IgG4 monoclonal antibody that binds to PD-1, preventing its interaction with PD-L1 and PD-L2 to enhance the immune system's ability to detect and destroy cancer cells. This triple-modality approach is currently being compared against HAIC-based combination therapies in clinical trials led by investigator Wen Li.

Brand names
CalliSpheresLenvimaTevimbra
Other names
D-TACE-Wen Li-hepatocellular carcinomaD-TACE plus lenvatinib and tislelizumabD-TACE-L-T
02

Targets

FGFR4 (Fibroblast growth factor receptor 4)PDCD1 (Programmed cell death protein 1 receptor)PDGFRA (Platelet-derived growth factor receptor alpha)TOP2A (DNA topoisomerase II)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)DNAVEGFR3 (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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