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modified FOLFIRINOX + gemcitabine

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

Overview

Modified FOLFIRINOX + gemcitabine is a combination chemotherapy regimen used primarily in the treatment of pancreatic cancer. Modified FOLFIRINOX consists of four drugs—folinic acid (leucovorin), fluorouracil (5-FU), irinotecan, and oxaliplatin—administered at reduced doses to improve tolerability compared to standard FOLFIRINOX. Gemcitabine is a nucleoside analog that inhibits DNA synthesis. This combination may be considered for patients with advanced or unresectable pancreatic cancer, particularly after progression on first-line therapy or in specific clinical trial settings. The mechanism of action involves multiple pathways targeting DNA synthesis and repair, leading to inhibition of tumor cell proliferation and survival[1][2][4][5].

Other names
modified FOLFIRINOX plus gemcitabinemFOLFIRINOX + gemcitabine
02

Targets

TS (Thymidylate synthase)TOP1 (DNA Topoisomerase I)DHFR (Dihydrofolate reductase)RNR (Ribonucleotide reductase)DNA

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