Drug intelligence / Profile preview

5-fluorouracil + interleukin-2 + levofolinic acid

Development stage
Unknown
Modality
Cytokines & Interferons → Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

This is a combination regimen consisting of three agents: - **5-fluorouracil (5-FU):** A pyrimidine analog antimetabolite that inhibits thymidylate synthase, disrupting DNA synthesis and leading to cell death in rapidly dividing cells. - **Interleukin-2 (IL-2):** A cytokine immunotherapy that stimulates the proliferation and activation of T lymphocytes and natural killer (NK) cells, enhancing immune-mediated tumor cell killing. - **Levofolinic acid (levoleucovorin):** The active enantiomer of folinic acid; it enhances the binding of 5-FU to thymidylate synthase, increasing its cytotoxicity against cancer cells. This combination has been studied as a salvage or second-line treatment for metastatic colorectal carcinoma refractory to previous chemotherapy. The addition of low-dose IL-2 aims to boost immune response without significantly increasing toxicity. Levofolinic acid potentiates the effect of 5-FU by stabilizing its binding to thymidylate synthase[1][6][8].

Other names
5-FU + IL-2 + levofolinic acidfluorouracil + recombinant interleukin-2 + levoleucovorin5-fluorouracil + rIL-2 + levoleucovorin
02

Targets

IL-2R (Interleukin-2/interleukin-15 receptor complex)TS (Thymidylate synthase)

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