Johannes Hofland

Applying 177Lu-Dotatate for Hereditary Neuroendocrine Tumours: The Role in MEN1

Abstract Introduction Multiple endocrine neoplasia type 1 (MEN1) is the most common genetic syndrome causing neuroendocrine tumours (NET) with metastatic duodenopancreatic NET (dpNET) forming the predominant cause of MEN1-related mortality. Peptide receptor radionuclide therapy w...