Published online Jun 14, 2015. doi: 10.3748/wjg.v21.i22.6785
Peer-review started: January 21, 2015
First decision: February 10, 2015
Revised: February 22, 2015
Accepted: April 16, 2015
Article in press: April 17, 2015
Published online: June 14, 2015
Processing time: 149 Days and 10.4 Hours
Gastric carcinoids (GCs) are classified as: type I, related to hypergastrinemia due to chronic atrophic gastritis (CAG), type II, associated with Zollinger-Ellison syndrome in multiple endocrine neoplasia type 1, and type III, which is normogastrinemic. The management of type-I gastric carcinoids (GC1s) is still debated, because of their relatively benign course. According to the European Neuroendocrine Tumor Society guidelines endoscopic resection is indicated whenever possible; however, it is not often feasible because of the presence of a multifocal disease, large lesions, submucosal invasion or, rarely, lymph node involvement. Therefore, somatostatin analogs (SSAs) have been proposed as treatment for GC1s in view of their antisecretive, antiproliferative and antiangiogenic effects. However, in view of the high cost of this therapy, its possible side effects and the relatively benign course of the disease, SSAs should be reserved to specific subsets of “high risk patients”, i.e., those patients with multifocal or recurrent GCs. Indeed, it is reasonable that, after the development of a gastric neuroendocrine neoplasm in patients with a chronic predisposing condition (such as CAG), other enterochromaffin-like cells can undergo neoplastic proliferation, being chronically stimulated by hypergastrinemia. Therefore, definite indications to SSAs treatment should be established in order to avoid the undertreatment or overtreatment of GCs.
Core tip: The management of type-I gastric carcinoids is still debated because of their relatively benign course against the fact that they can have a heterogeneous unpredictable biological behavior. Even if in most cases their endoscopic treatment is effective, in some particular cases it may not be sufficient. The potential role of somatostatin analogs (SSAs) has been reported in several recent studies. However, neither a standard indication nor a specific schedule of treatment with defined dosage and duration have been adopted to date. Because of the high cost of SSAs, clear-cut indications for this therapy are required in order to avoid any overtreatment.