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tislelizumab + lenvatinib + irinotecan liposomes
- Development stage
- Unknown
- Lead developer
- BeiGene
- Modality
- Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
- Administration
- Intravenous, Oral
01
Overview
This combination therapy consists of the PD-1 inhibitor tislelizumab, the multi-kinase inhibitor lenvatinib, and a liposomal formulation of the cytotoxic agent irinotecan. It is being investigated by the Anhui Provincial Cancer Hospital for the treatment of advanced or metastatic esophageal squamous cell carcinoma (ESCC). Tislelizumab is a humanized IgG4 monoclonal antibody that enhances the anti-tumor immune response by blocking the PD-1/PD-L1 pathway. Lenvatinib targets multiple receptor tyrosine kinases, including VEGFR and FGFR, to inhibit angiogenesis and tumor cell proliferation, while also potentially modulating the tumor microenvironment to enhance immunotherapy. Irinotecan liposomes provide a sustained-release formulation of the topoisomerase I inhibitor, leading to DNA damage and apoptosis in rapidly dividing cancer cells. The regimen aims to provide synergistic anti-tumor activity through immune activation, anti-angiogenesis, and direct cytotoxicity.
- Other names
- tislelizumab + renvastinib + irinotecan liposomes
02
Targets
FGFR4 (Fibroblast growth factor receptor 4)PDCD1 (Programmed cell death protein 1 receptor)PDGFRA (Platelet-derived growth factor receptor alpha)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)TOP1 (DNA Topoisomerase I)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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