4.5 Review

Radionuclide Therapy for Neuroendocrine Tumors

期刊

CURRENT ONCOLOGY REPORTS
卷 19, 期 2, 页码 -

出版社

SPRINGER
DOI: 10.1007/s11912-017-0567-8

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Carcinoid tumors; PRRT; Radiolabeled somatostatin analogs; Lutetium; NETTER-1

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  1. Novartis
  2. Advanced Accelerator Applications

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Peptide receptor radionuclide therapy (PRRT) is a form of systemic radiotherapy that allows targeted delivery of radionuclides to tumor cells expressing high levels of somatostatin receptors. The two radiopeptides most commonly used for PRRT, Y-90-DOTATOC and Lu-177-DOTATATE, have been successfully employed for more than a decade for the treatment of advanced neuroendocrine tumors (NETs). Recently, the phase III, randomized NETTER-1 trial has compared Lu-177-DOTATATE versus high-dose octreotide LAR in patients with progressive, metastatic midgut NETs, demonstrating exceptional tolerability and efficacy. This review summarizes recent developments in the field of radionuclide therapy for gastroenteropancreatic and lung NETs and considers possible strategies to further enhance its clinical efficacy.

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