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chemotherapy of mFOLFOX6 or FOLFIRI

Xu jianmin · FDA-approved active Small molecule

mFOLFOX6 and FOLFIRI are combination chemotherapy regimens that inhibit DNA synthesis and cell division through multiple mechanisms targeting rapidly dividing cancer cells.

mFOLFOX6 and FOLFIRI are combination chemotherapy regimens that inhibit DNA synthesis and cell division through multiple mechanisms targeting rapidly dividing cancer cells. Used for Metastatic colorectal cancer, Adjuvant treatment of stage III colorectal cancer, Gastric cancer.

At a glance

Generic namechemotherapy of mFOLFOX6 or FOLFIRI
Also known asmFOLFOX6
SponsorXu jianmin
Drug classCombination chemotherapy regimen
TargetThymidylate synthase (5-FU), DNA topoisomerase I (irinotecan), DNA (oxaliplatin)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

mFOLFOX6 combines 5-fluorouracil (5-FU), leucovorin, and oxaliplatin to inhibit thymidylate synthase and cause DNA crosslinking. FOLFIRI substitutes irinotecan (a topoisomerase I inhibitor) for oxaliplatin. Both regimens work synergistically to prevent cancer cell proliferation and induce apoptosis in colorectal and other solid tumors.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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