Drug intelligence / Profile preview

sunitinib + oxaliplatin + capecitabine

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

**Sunitinib + oxaliplatin + capecitabine** is an investigational combination regimen studied primarily for advanced gastric cancer. It combines: - **Sunitinib**, a small-molecule multi-targeted receptor tyrosine kinase inhibitor that blocks cellular signaling by targeting several kinases, including vascular endothelial growth factor receptor (VEGF-R), platelet-derived growth factor receptor (PDGF-R), KIT, FLT3, RET, and CSF-1R[9]. This leads to antiangiogenic and direct antitumor activity. - **Oxaliplatin**, a platinum-based chemotherapeutic agent that forms DNA crosslinks, inhibiting DNA replication and transcription, thereby causing cell death[1][3][7]. - **Capecitabine**, an oral prodrug of 5-fluorouracil (5-FU), inhibits thymidylate synthase, impairing DNA synthesis and leading to cell death in rapidly dividing cells[1][3][7]. Used together, the regimen exhibits additive or synergistic antitumor and antiangiogenic effects. The primary indication studied is advanced gastric cancer, with ongoing investigation for other solid tumors[4][5][8].

Brand names
Sutent (for sunitinib)Xeloda (for capecitabine)sunitinib + oxaliplatin + capecitabine
Other names
XELOX + sunitinibsunitinib/XELOXsunitinib plus oxaliplatin plus capecitabine
02

Targets

TS (Thymidylate synthase)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)CSF1R (Macrophage colony-stimulating factor receptor)PDGFRB (Platelet-derived growth factor receptor beta)DNAVEGFR3 (Vascular endothelial growth factor receptor 3)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)

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