FLOX (Not branded (combination regimen))

Chemotherapy · Approved since 2002

US FDA Approved IV 2 Clinical Trials

Description

FLOX is a combination chemotherapy regimen consisting of 5-fluorouracil (5-FU), leucovorin (folinic acid), and oxaliplatin used in the treatment of colorectal cancer. This regimen is primarily employed in the adjuvant setting following surgical resection of colorectal tumors and in patients with metastatic disease. FLOX combines the antimetabolite activity of 5-FU with the platinum-based cytotoxicity of oxaliplatin, while leucovorin enhances 5-FU's efficacy. The regimen has demonstrated effectiveness in improving disease-free survival in stage II and III colorectal cancer patients.

Mechanism of Action

This combination targets rapidly dividing cancer cells through complementary mechanisms of DNA damage and metabolic disruption. 5-fluorouracil acts as a pyrimidine analog that interferes with DNA synthesis and RNA processing by inhibiting thymidylate synthase, while leucovorin enhances this effect by stabilizing the 5-FU-thymidylate synthase complex. Oxaliplatin forms DNA crosslinks by binding to purine bases, creating bulky platinum-DNA adducts that trigger apoptosis in cancer cells.

Side Effects

Peripheral neuropathy Nausea and vomiting Diarrhea Fatigue Neutropenia Thrombocytopenia Mucositis Hand-foot syndrome

Not all side effects are listed. Side effects vary by individual. Always consult your oncologist.

Clinical Trials

NCT03500874 Phase 3
Archived
Adjuvant Systemic Chemotherapy With or Without HAI-FUDR in Patients With Resected CRLM
China
NCT01815359 Phase 2
Active, not recruiting
ICARuS Post-operative Intraperitoneal Chemotherapy (EPIC) and Hyperthermic Intraperitoneal Chemotherapy (HIPEC) After Optimal Cytoreductive Surgery (CRS) for Neoplasms of the Appendix, Colon or Rectum With Isolated Peritoneal Metastasis
United States