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

177Lu dotatate peptide receptor radionuclide therapy (PRRT) is approved by the FDA for the treatment of somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (GEP-NETs), including foregut, midgut, and hindgut neuroendocrine tumors.
PRRT with 177Lu dotatate binds to somatostatin receptors found on neuroendocrine tumor cells. The attached radionuclide delivers targeted radiation to kill these tumor cells. Specifically, 177Lu emits beta radiation to damage tumor cell DNA, ultimately destroying malignant cells.

The FDA approval was based on the results of the NETTER-1 phase 3 clinical trial. This trial demonstrated:



Indications

177Lu dotatate PRRT is approved for:



Essentially, 177Lu dotatate PRRT is approved for treatment of GEP-NETs except those originating from the rectum. Approximately 90% of GEP-NETs and 80-90% of lung NETs express somatostatin receptors detectable by an octreotide scan and are thus eligible for PRRT.

Contraindications



At Renewal Hormone Clinic, we offer cutting-edge PRRT with 177Lu dotatate for qualifying patients with metastatic, progressive NETs. Our world-class nuclear medicine physicians have extensive experience using advanced molecular imaging and therapies to treat cancer. Contact us today to find out if you are eligible for this innovative therapy.

This therapy represents a major advancement in the treatment paradigm for NETs. By harnessing the power and precision of molecular medicine, targeted radiotherapy provides outcomes unattainable with traditional chemotherapy. With an acceptable safety profile and proven efficacy for prolonging progression-free survival, 177Lu dotatate PRRT fills an important unmet need for patients with somatostatin receptor-positive GEP-NETs and lung NETs.

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