Featured ArticleCaring for Patients Receiving 177Lu-DOTATATE, Lutathera®: A Treatment of Hope for Patients With Gastroenteropancreatic Neuroendocrine Tumors
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Lutathera® and GEP-NETs
Lutathera®, the trademark for 177Lu-DOTATATE registered to Advanced Accelerator Applications, SA, Millburn, NJ, is a peptide receptor radionuclide therapy (PRRT) medicine used to treat gastroenteropancreatic neuroendocrine tumors (GEP-NETs) positive for hormone receptor somatostatin (Lui, 2015, LUTATHERA, 2018, Strosberg et al., 2017) (Box 1). Lutathera PRRT is an internal radioactive therapy in which 177Lu (lutetium), a radioactive isotope with a half-life of 6-7 days, is bonded to the amino
Potential adverse effects of Lutathera
Lutathera contributes to the overall radiation exposure that patients experience in their life time, and this cumulative radiation exposure is known to increase the risks for certain cancers. The most frequently identified adverse effects found in the phase 3 trial of Lutathera were gastrointestinal symptoms such as nausea, vomiting, and diarrhea, as well as abdominal pain and distension (Strosberg et al., 2017). Most patients reported these as symptoms in conjunction with the amino acids, with
Prescreening
During the prescreening process by the nuclear medicine physicians who will administer the Lutathera, patient preparation for treatment has already begun. Prescreening criteria include a known GEP-NET, positive diagnostic IN-111 Octeoscan or 68 GA-Dotatate scans, and that the patient is ≥18 years of age. Diagnostic scans confirm the GEP-NET receptor positive, thus indicating an expected uptake of 177Lu-DOTATATE by the tumor. In addition, pretreatment blood work needs to be evaluated
Conclusion—treatment of hope
Teamwork and collaboration among departments of nuclear medicine staff, radiation-safety personnel, radiology nursing, and the physicians are needed to successfully treat patients with GEP-NETs using the now FDA-approved Lutathera treatment process. Advanced Accelerator Applications (2018) provides detailed prescribing information to facilitate the creation of institution-specific policies and procedures for the administration of Lutathera while protecting patients and caregivers. Detailed and
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This work is unfunded and has not been previously presented.
Both authors declare no conflicts of interest.
No grant funding received.