Drug intelligence / Profile preview

Sorafenib + FOLFIRI

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

Overview

Sorafenib + FOLFIRI is a combination regimen used in oncology clinical trials, particularly for advanced gastrointestinal malignancies such as colorectal cancer. Sorafenib is an oral small molecule multikinase inhibitor that targets several serine/threonine and tyrosine kinases, including all vascular endothelial growth factor receptors (VEGFR), Raf kinases, platelet-derived growth factor receptor beta (PDGFR-β), and fibroblast growth factor receptor 1 (FGFR1). This results in inhibition of tumor cell proliferation and angiogenesis. FOLFIRI is a chemotherapy regimen consisting of folinic acid (leucovorin), fluorouracil (5-FU), and irinotecan. Fluorouracil acts as an antimetabolite inhibiting DNA synthesis; irinotecan inhibits topoisomerase I, preventing DNA replication; folinic acid enhances the effect of fluorouracil. The combination aims to provide both cytotoxic effects from chemotherapy and antiangiogenic/antiproliferative effects from sorafenib[1][4][6][8].

Brand names
Nexavar
Other names
sorafenibfolinic acid, fluorouracil and irinotecanirinotecan de Gramontirinotecan modified de Gramont
02

Targets

TS (Thymidylate synthase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)TOP1 (DNA Topoisomerase I)RAF1 (c-Raf-1 (Y340D/Y341D))VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR1 (Fibroblast growth factor receptor 1)FLT3 (Fms related receptor tyrosine kinase 3)

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