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lenvatinib + epirubicin
- Development stage
- Unknown
- Lead developer
- Eisai
- Modality
- Small Molecules
- Administration
- Oral, Intravenous
01
Overview
Lenvatinib + epirubicin is an investigational combination therapy comprising the multi-kinase inhibitor lenvatinib and the anthracycline chemotherapy agent epirubicin. Lenvatinib functions by inhibiting several receptor tyrosine kinases, including VEGFR1-3, FGFR1-4, PDGFRα, KIT, and RET, thereby suppressing tumor angiogenesis and proliferation. Epirubicin exerts its cytotoxic effect by intercalating into DNA and inhibiting topoisomerase II, which leads to DNA strand breaks and apoptosis. This combination is primarily being developed by The Second Affiliated Hospital of Air Force Medical University for the treatment of radioactive iodine-refractory differentiated thyroid cancer (RAIR-DTC), aiming to improve outcomes in patients who have failed standard treatments.
- Other names
- lenvatinib plus epirubicin
02
Targets
FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)TOP2A (DNA topoisomerase II)FGFR3 (Fibroblast growth factor receptor 3)DNAVEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)FGFR2 (Keratinocyte growth factor receptor)
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