Drug intelligence / Profile preview

TACE + lenvatinib + microwave ablation

Development stage
Unknown
Lead developer
Sun Yat-sen University Cancer Center
Modality
Small Molecules
Administration
Oral, Intra-arterial, Interstitial
01

Overview

This combination treatment regimen, investigated in the TALEM trial (NCT05555316) by Sun Yat-sen University Cancer Center, is designed for patients with large unresectable hepatocellular carcinoma (HCC) (≥7 cm). The regimen consists of modified transarterial chemoembolization using blank microspheres with low-dose chemotherapy (BMS-TACE), followed by oral administration of the multi-kinase inhibitor lenvatinib, and sequential radical microwave ablation (MWA) once downstaging is achieved. Lenvatinib targets VEGFR1-3, FGFR1-4, PDGFRα, RET, and KIT to inhibit angiogenesis and tumor cell proliferation. The TACE component typically involves lipiodol, low-dose doxorubicin, and lobaplatin. The regimen aims to convert unresectable large tumors into candidates for curative ablation, showing high objective response and downstaging rates in clinical studies.

Other names
BMS-TACE + lenvatinib + MWATACE combined with Lenvatinib and MWA
02

Targets

FGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)FGFR3 (Fibroblast growth factor receptor 3)FGFR4 (Fibroblast growth factor receptor 4)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)DNA

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