Pylarify, with the generic name piflufolastat F 18, is a diagnostic radiopharmaceutical used in conjunction with PET scans to detect prostate-specific membrane antigen (PSMA) positive lesions in men with prostate cancer. Pylarify was approved by the U.S. Food and Drug Administration (FDA) on May 26, 2021. This approval marked a significant advancement in the imaging and diagnosis of prostate cancer, providing a critical tool for clinicians in managing the disease.
Pylarify is used specifically for:
As a radiopharmaceutical, Pylarify consists of a radioactive agent used to visualize and track biological processes in the body. When administered, it binds to PSMA, a protein often overexpressed in prostate cancer cells. This binding enables PET scans to detect the location and extent of cancer within the body.
Pylarify is administered intravenously by a healthcare professional shortly before a PET scan. Proper hydration before the scan is recommended, and patients are advised to urinate frequently following the scan to help expel the radioactive agent from the body.
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Pylarify represents a significant advancement in the diagnostic imaging of prostate cancer. Its ability to precisely detect PSMA-positive lesions aids in the accurate assessment of cancer spread and recurrence, making it a vital tool for clinicians managing prostate cancer. Despite its benefits, it is essential to consider the potential risks and side effects associated with its use.
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