Therapy Resistant Gastroenteropancreatic Neuroendocrine Tumors

Simple Summary The medical care for patients with neuroendocrine tumors arising from the intestines, pancreas, or stomach is frequently limited by the development resistance to common treatment approaches including targeted therapies and chemotherapy. The purpose of this review is to summarize the current treatments for these tumors, the possible cellular changes involved with the development of treatment resistance, and possible ways to overcome or approach this challenge. The goal is to provide an up to date summary of current and upcoming clinical findings regarding therapy-resistant neuroendocrine tumors. Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are a heterogenous group of malignancies originating from neuroendocrine cells of the gastrointestinal tract, the incidence of which has been increasing for several decades. While there has been significant progress in the development of therapeutic options for patients with advanced or metastatic disease, these remain limited both in quantity and durability of benefit. This review examines the latest research elucidating the mechanisms of both up-front resistance and the eventual development of resistance to the primary systemic therapeutic options including somatostatin analogues, peptide receptor radionuclide therapy with lutetium Lu 177 dotatate, everolimus, sunitinib, and temozolomide-based chemotherapy. Further, potential strategies for overcoming these mechanisms of resistance are reviewed in addition to a comprehensive review of ongoing and planned clinical trials addressing this important challenge.

Automated summary

This review summarizes the current treatments for neuroendocrine tumors and explores the cellular changes involved in treatment resistance. It provides an up-to-date summary of clinical findings regarding therapy-resistant neuroendocrine tumors and discusses potential strategies to overcome resistance.