For which indications are 177lu Dotatate peptide receptor radionuclide therapy approved by the FDA? - Balanced Hormone Clinic

177Lu Dotatate, also known as Lutathera, is a radiolabeled somatostatin analog peptide approved by the FDA for the treatment of somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (GEP-NETs) in adults. Some key points about Lutathera's FDA-approved indications:

The National Comprehensive Cancer Network (NCCN) guidelines also recommend Lutathera as a systemic therapy option for: The peptide in Lutathera, DOTA-Tyr3-octreotate, targets somatostatin receptors (particularly sst2) which are overexpressed in certain NETs cells. By targeting these receptors, the attached radionuclide 177Lu delivers radiation directly the tumor cells. The Balanced Hormone Clinic Hormone Clinic offers comprehensive cancer care for patients, including those with GEP-NETs who may be candidates for peptide receptor radionuclide therapy. Our cancer specialists will conduct a full medical evaluation to determine if targeted radionuclide therapy is an appropriate treatment option. If eligible for 177Lu Dotatate therapy, patients undergo rigorous monitoring after each Lutathera infusion, including bloodwork and imaging, to closely track treatment response. We also provide nutritional guidance and symptom management throughout therapy to maintain health and quality of life while fighting cancer. Contact Balanced Hormone Clinic today to find out if you or loved one could benefit from 177Lu-Dotatate therapy administered by leading NETs experts. In summary, key points about FDA-approved indications for 177Lu Dotatate include: Reach out to the experts at Balanced Hormone Clinic Hormone Clinic to find out if targeted 177Lu Dotatate therapy is right for you or your loved one's GEP-NET.

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