♦Floxuridine



♦Floxuridine





(flox-yur’-i-deen)

FUDR

Pregnancy Category D


Mechanism of Action

Floxuridine is a cytotoxic antimetabolite that acts primarily by interfering with the synthesis of DNA; to a lesser extent, it inhibits the formation of RNA.


Indications

Palliative management of GI adenocarcinoma metastatic to the liver (when given by regional intra-arterial infusion) for patients considered incurable by surgery or other means.


Metabolism/Excretion

Metabolized in the liver; excreted in the urine; also expired as respiratory carbon dioxide. It has a biphasic half-life: initial = 10 to 20 minutes; terminal = 20 hours.


Dosage Range

♦ Adult: 0.1 to 0.6 mg/kg per day. If is given by hepatic artery infusion, the dosage is 0.4 to 0.6 mg/kg per day because the liver metabolizes the drug, reducing systemic
toxicities. Therapy can continue when side effects have resolved and should be maintained as long as a therapeutic response is observed.

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Jul 20, 2016 | Posted by in ONCOLOGY | Comments Off on ♦Floxuridine

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