Drug intelligence / Profile preview

mFOLFOX + FOLFIRI

Development stage
Unknown
Modality
DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules
Administration
Intravenous
01

Overview

mFOLFOX + FOLFIRI is a combination chemotherapy regimen used primarily in the treatment of advanced or metastatic colorectal cancer. It consists of two established regimens administered either sequentially or in an alternating fashion: - **mFOLFOX (modified FOLinic acid, Fluorouracil, OXaliplatin):** - Folinic acid (leucovorin): Enhances the cytotoxic effect of fluorouracil. - Fluorouracil (5-FU): An antimetabolite that inhibits DNA synthesis by incorporating into DNA and RNA. - Oxaliplatin: A platinum-based agent that causes DNA crosslinking and apoptosis. - **FOLFIRI (Folinic acid, Fluorouracil, IRInotecan):** - Folinic acid (leucovorin) - Fluorouracil (5-FU) - Irinotecan: A topoisomerase I inhibitor that prevents DNA replication. The mechanism of action involves targeting rapidly dividing cancer cells through multiple pathways—disruption of DNA synthesis/replication and enhancement of cytotoxicity. This combination is typically reserved for patients with metastatic colorectal cancer who require intensive systemic therapy[1][3][6]. The regimen may be used as part of first-line or subsequent lines depending on patient characteristics and prior treatments.

Other names
modified FOLFOX plus FOLFIRIsequential mFOLFOX and FOLFIRIalternating mFOLFOX/FOLFIRI
02

Targets

TS (Thymidylate synthase)TOP1 (DNA Topoisomerase I)DNA

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