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

177Lu Dotatate (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. Specifically, it is indicated for:

Key details: The approval was based on the pivotal NETTER-1 phase III trial, which demonstrated: 177Lu Dotatate emits beta radiation, which penetrates just a short distance, limiting damage to nearby healthy tissues. Most common adverse effects are: These are generally manageable with antiemetics, growth factors, and supportive care. At Elite Hormone Therapy, we offer cutting-edge peptide receptor radionuclide therapy for NETs and other neuroendocrine tumors. Our specialists have deep expertise in delivering systemic radiotherapy in a meticulously planned, precision-targeted approach to suppress tumor growth while minimizing side effects. We conduct thorough molecular profiling to identify patients most likely to benefit from 177Lu Dotatate therapy based on somatostatin receptor status. Our technologically advanced facilities and nuclear medicine expertise allow us to deliver customized therapy with optimal accuracy. Key elements of our approach include: If you or a loved one has been diagnosed with a neuroendocrine tumor, consider being evaluated for 177Lu Dotatate therapy at Elite Hormone Therapy. Contact our team today to learn more about how this innovative therapy could help control the growth of inoperable or metastatic NETs.

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