New Treatments for the Carcinoid Syndrome

Abstract

Neuroendocrine tumors, including carcinoids, are rare and insidiously growing tumors. Related to their site of origin, tumors can be functional, causing various forms of the carcinoid syndrome, owing to the overproduction of serotonin, histamine, or other bioactive substances. They often invade adjacent structures or metastasize to the liver and elsewhere. Treatment includes multimodal approaches, including cytoreductive surgery, locoregional embolization, cytotoxic therapy, peptide receptor radionuclide therapy, and various targeted therapies with goals of symptom relief and control of tumor growth. This article summarizes current and emerging approaches to management and reviews several promising future therapies.

Keywords: Everolimus; Medical treatment; Peptide receptor radionuclide therapy; Somatostatin receptor ligands; Sunitinib; Surgery; Telotristat etiprate; Theranostics.