In recent years, there has been a significant rise in neuroendocrine tumor incidence. For instance, they account for around 2% of all malignancies in the United States. Medical professionals employ various treatment approaches to combat these tumors. One such novel and effective treatment is the peptide receptor radionuclide therapy.
Peptide receptor radionuclide therapy has become a breakthrough treatment for NETs. It ensures targeted delivery of radiation to NET cells expressing somatostatin receptors. Lutetium-177 dotatate (Lutathera) is a widely used radiopharmaceutical in PRRT.
How PRRT Works in Neuroendocrine Tumors?
Peptide receptor radionuclide therapy (PRRT) is a type of molecular radiotherapy that targets specific receptor molecules on particular cancer cells. It utilizes radioactive drugs to treat neuroendocrine tumors.
In PRRT, a radioactive chemical is attached to a peptide that targets cancer cells. It uses synthetic somatostatin analogs that are radiolabeled. These radiolabelled analogs bind to somatostatin receptors on the NET cells, delivering radiation directly to the tumor. The radioactive isotope emits radiation that damages DNA of NET cells, causing their destruction.
Role of PRRT in Neuroendocrine Tumor Treatment
PRRT is mostly used to treat advanced NETs like gastroenteropancreatic NETs. It has the potential to slow or stop tumor growth. By doing so, it can help to relieve symptoms and improve the quality of life for patients with advanced NETs.
PRRT is highly effective for NETs that overexpress somatostatin receptors. It only targets tumor cells without affecting normal tissues. This makes it ideal for NET management.
The NETTER-2 trial demonstrated that Lutathera can improve progression-free survival of patients with grade 2 or 3 advanced neuroendocrine tumors.
Certain NETs can cause hormonal syndromes like carcinoid syndrome. PRRT can help to combat this by reducing tumor growth and reproduction.
