Drug intelligence / Profile preview

intraperitoneal fluorouracil + FOLFOX

Development stage
Discontinued
Lead developer
Washington University School of Medicine
Modality
Small Molecules
Administration
Intraperitoneal, Intravenous
01

Overview

This treatment protocol, evaluated in a Phase II clinical trial by Washington University School of Medicine, combines cytoreductive surgery (peritonectomy) with a multimodal chemotherapy regimen. It involves the repeated, delayed intraperitoneal administration of fluorouracil (5-FU) alongside systemic FOLFOX chemotherapy (a combination of oxaliplatin, leucovorin, and fluorouracil). Fluorouracil acts as a pyrimidine analog that inhibits thymidylate synthase, thereby disrupting DNA synthesis. Oxaliplatin is a platinum-based antineoplastic agent that forms DNA adducts, leading to inter- and intra-strand cross-links that inhibit DNA replication and transcription. This dual-route approach is designed to treat peritoneal surface malignancies, such as pseudomyxoma peritonei and peritoneal carcinomatosis, by providing high local concentrations of chemotherapy within the peritoneal cavity while simultaneously addressing potential systemic micrometastases.

Other names
IP 5-FU + FOLFOXIntraperitoneal 5-fluorouracil and systemic FOLFOXIntraperitoneal5-fluorouracil and systemic FOLFOXIntraperitoneal-5-fluorouracil and systemic FOLFOXIP 5FU and FOLFOX for Peritoneal MalignanciesIP5FU and FOLFOX for Peritoneal MalignanciesIP-5FU and FOLFOX for Peritoneal Malignancies
02

Targets

TS (Thymidylate synthase)DNA

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