Drug intelligence / Profile preview

sunitinib + sorafenib + bevacizumab + pazopanib

Development stage
Unknown
Lead developer
Pfizer
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
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Overview

Sunitinib + sorafenib + bevacizumab + pazopanib is a theoretical combination of four anti-cancer agents, each individually used in the management of advanced renal cell carcinoma (RCC). Sunitinib, sorafenib, and pazopanib are small molecule multi-targeted receptor tyrosine kinase (RTK) inhibitors. They primarily work by blocking various kinases involved in tumor growth and angiogenesis, such as vascular endothelial growth factor receptors (VEGFRs), platelet-derived growth factor receptors (PDGFRs), and c-KIT. Sorafenib also inhibits RAF kinases. Bevacizumab is a recombinant humanized monoclonal antibody that specifically targets vascular endothelial growth factor A (VEGF-A), thereby inhibiting angiogenesis (the formation of new blood vessels that supply tumors). This combination, while comprising agents used in RCC treatment, is not a standard or approved fixed-dose regimen due to significant overlap in mechanisms and potential for cumulative toxicities.

02

Targets

FGFR1 (Fibroblast growth factor receptor 1)FLT3 (Fms related receptor tyrosine kinase 3)PDGFRB (Platelet-derived growth factor receptor beta)VEGFA (Vascular endothelial growth factor A)VEGFR2 (Vascular endothelial growth factor receptor 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR3 (Fibroblast growth factor receptor 3)PDGFRA (Platelet-derived growth factor receptor alpha)RAF1 (c-Raf-1 (Y340D/Y341D))RET (Rearranged during transfection receptor tyrosine kinase)BRAF (B-Raf proto-oncogene, serine/threonine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR4 (Vascular endothelial growth factor Receptor-3)

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