Review article: the investigation and management of gastric neuroendocrine tumours

Summary Background Gastric carcinoids (GCs) or neuroendocrine tumours (NETs) are increasingly identified at endoscopy, and account for 0.6–2% of all gastric polyps identified. The SEER database in the US has demonstrated a rising incidence of gastric NETs amongst all NETs; from 2.2% between 1950 and...

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Bibliographic Details
Published in:Alimentary pharmacology & therapeutics 2014-05, Vol.39 (10), p.1071-1084
Main Authors: Basuroy, R., Srirajaskanthan, R., Prachalias, A., Quaglia, A., Ramage, J. K.
Format: Article
Language:English
Subjects:
Biological and medical sciences
Dissection - methods
Endoscopy - methods
Gastrins
Gastritis, Atrophic - pathology
Gastritis, Atrophic - therapy
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Medical sciences
Neuroendocrine Tumors - diagnosis
Neuroendocrine Tumors - pathology
Neuroendocrine Tumors - therapy
Polyps - pathology
Prognosis
Stomach Neoplasms - diagnosis
Stomach Neoplasms - pathology
Stomach Neoplasms - therapy
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Tumors
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Summary:Summary Background Gastric carcinoids (GCs) or neuroendocrine tumours (NETs) are increasingly identified at endoscopy, and account for 0.6–2% of all gastric polyps identified. The SEER database in the US has demonstrated a rising incidence of gastric NETs amongst all NETs; from 2.2% between 1950 and 1969 to 6.0% between 2000 and 2007. Aim To review the literature and assist clinicians in managing patients with GCs. Methods A literature search was conducted through MEDLINE using search terms: gastric, carcinoid, neuroendocrine tumour, therapy, endoscopy, mucosal resection, submucosal dissection. Relevant articles were identified through manual review. The reference lists of these articles were reviewed to include further appropriate articles. Results There are three types of GCs with important epidemiological, pathophysiological, histological and endoscopic differences that affect prognosis and management. Type 1 and 2 GCs develop in the context of hypergastrinaemia that originates from achlorhydria in atrophic gastritis and a gastrinoma, respectively. Type 3 GCs occur sporadically and independent of gastrin. The histological type, grade and Ki67 index are used to determine prognosis and direct clinical management. Type 1 GCs >1 cm in size and type 2 GCs should be assessed for invasion beyond the submucosa with EUS prior to endoscopic resection with EMR or ESD. Type 3 GCs should be managed as per recommendations for gastric adenocarcinoma. The treatment of advanced disease is multimodal. Conclusions Patients with gastric carcinoids should be discussed in a specialist neuroendocrine tumour multidisciplinary meeting to ensure all treatment options are explored in localised and advanced disease. Areas of controversy exist that need further research.
ISSN:0269-2813
1365-2036
DOI:10.1111/apt.12698