Fluciclovine F-18

From WikiMD's Wellness Encyclopedia

Information about the radiopharmaceutical Fluciclovine F-18


Fluciclovine F-18
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INN
Drug class
Routes of administration Intravenous
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number 902143-01-5
PubChem 71301030
DrugBank DB05283
ChemSpider 29341430
KEGG D10868


Fluciclovine F-18 is a radiopharmaceutical used in positron emission tomography (PET) imaging. It is primarily utilized for the detection of recurrent prostate cancer in patients with elevated prostate-specific antigen (PSA) levels following prior treatment.

Mechanism of Action[edit | edit source]

Fluciclovine F-18 is a synthetic amino acid analog that is taken up by amino acid transporters overexpressed in prostate cancer cells. The radiolabeled compound emits positrons that are detected by PET imaging, allowing for the visualization of cancerous lesions.

Clinical Use[edit | edit source]

Fluciclovine F-18 is indicated for use in patients with suspected prostate cancer recurrence based on elevated PSA levels. It provides a non-invasive method to localize recurrent disease, which can guide further therapeutic interventions.

Administration[edit | edit source]

The compound is administered via intravenous injection. The recommended dose is typically based on the patient's body weight and the specific imaging protocol.

Safety and Precautions[edit | edit source]

As with any radiopharmaceutical, there are potential risks associated with exposure to radiation. Patients should be informed of these risks, and the use of Fluciclovine F-18 should be justified by the potential diagnostic benefits.

Regulatory Status[edit | edit source]

Fluciclovine F-18 is approved by the Food and Drug Administration (FDA) for use in the United States. It is marketed under the trade name Axumin.

See Also[edit | edit source]

References[edit | edit source]


External Links[edit | edit source]

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Contributors: Prab R. Tumpati, MD