Clinicopathological characteristics and prognosis of 77 cases with type 3 gastric neuroendocrine tumours
- PMID: 33362912
- PMCID: PMC7739150
- DOI: 10.4251/wjgo.v12.i12.1416
Clinicopathological characteristics and prognosis of 77 cases with type 3 gastric neuroendocrine tumours
Abstract
Background: For the rarity of type 3 gastric neuroendocrine tumours (g-NETs), their clinicopathological characteristics and prognosis are not well illustrated.
Aim: To describe the clinicopathological features and outcome of type 3 g-NETs in the Chinese population.
Methods: Based on the 2019 WHO pathological classification, the clinicopathological characteristics and prognosis of patients with type 3 g-NETs in China were retrospectively analysed.
Results: A total of 77 patients (55.8% of females) with type 3 g-NETs were analysed, with a median age of 48 years (range: 28-79 years). The tumours were mainly located in the gastric fundus/body (83.1%) and were mostly solitary (83.1%), with a median size of 1.5 cm (0.8-3.5 cm). Of these, there were 37 G1 tumours (48.1%), 31 G2 (40.3%), and 9 G3 (11.7%). Ten (13.0%) and 24 (31.2%) patients had lymph node and distant metastasis, respectively. In addition, type 3 g-NETs were heterogeneous. Compared with G1 NETs, G2 NETs had a higher lymph node metastasis rate, and G3 NETs had a higher distant metastasis rate. G1 and G2 NETs with stage I/II disease (33/68) received endoscopic treatment, and no tumour recurrence or tumour-related death was observed within a median follow-up time of 36 mo. Grade and distant metastasis were identified to be independent risk factors for prognosis in multivariable analysis.
Conclusion: Type 3 g-NETs are obviously heterogeneous, and the updated WHO 2019 pathological classification may be used to effectively evaluate their biological behaviors and prognosis. Also, endoscopic treatment should be considered for small (< 2 cm), low grade, superficial tumours.
Keywords: Chinese population; Clinicopathological characteristics; Endoscopic treatment; Prognosis; Type 3 gastric neuroendocrine tumours.
©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved.
Conflict of interest statement
Conflict-of-interest statement: The authors declare that no competing interests exist.
Figures
Similar articles
-
Clinicopathological features and outcome of type 3 gastric neuroendocrine tumours.Br J Surg. 2018 Oct;105(11):1480-1486. doi: 10.1002/bjs.10901. Epub 2018 Jun 12. Br J Surg. 2018. PMID: 29893418
-
[Clinicopathologic features and prognostic analysis of 240 patients with gastric neuroendocrine neoplasms].Zhonghua Wei Chang Wai Ke Za Zhi. 2020 Jan 25;23(1):38-43. doi: 10.3760/cma.j.issn.1671-0274.2020.01.007. Zhonghua Wei Chang Wai Ke Za Zhi. 2020. PMID: 31958929 Chinese.
-
[Subtype classification and clinicopathological characteristics of gastric neuroendocrine neoplasms: an analysis of 241 cases].Zhonghua Wei Chang Wai Ke Za Zhi. 2016 Nov 25;19(11):1241-1246. Zhonghua Wei Chang Wai Ke Za Zhi. 2016. PMID: 27928793 Chinese.
-
Systematic review: management of localised low-grade upper gastrointestinal neuroendocrine tumours.Aliment Pharmacol Ther. 2020 Jun;51(12):1247-1267. doi: 10.1111/apt.15765. Epub 2020 May 11. Aliment Pharmacol Ther. 2020. PMID: 32390152
-
Management of gastric and duodenal neuroendocrine tumors.World J Gastroenterol. 2016 Aug 14;22(30):6817-28. doi: 10.3748/wjg.v22.i30.6817. World J Gastroenterol. 2016. PMID: 27570419 Free PMC article. Review.
Cited by
-
Endoscopic techniques for gastric neuroendocrine tumors: An update.World J Gastrointest Endosc. 2023 Mar 16;15(3):103-113. doi: 10.4253/wjge.v15.i3.103. World J Gastrointest Endosc. 2023. PMID: 37034968 Free PMC article. Review.
-
Modern Management of Gastric Neuroendocrine Neoplasms.Curr Treat Options Oncol. 2024 Sep;25(9):1137-1152. doi: 10.1007/s11864-024-01207-2. Epub 2024 Jul 31. Curr Treat Options Oncol. 2024. PMID: 39083164 Review.
-
Advances in Endoscopic Diagnosis and Treatment of Gastric Neuroendocrine Neoplasms.Dig Dis Sci. 2024 Jan;69(1):27-35. doi: 10.1007/s10620-023-08180-0. Epub 2023 Nov 16. Dig Dis Sci. 2024. PMID: 37971578 Review.
-
Gastric Neuroendocrine Tumors and Pernicious Anemia: A Case Report and Literature Review.Cureus. 2024 Nov 12;16(11):e73553. doi: 10.7759/cureus.73553. eCollection 2024 Nov. Cureus. 2024. PMID: 39669826 Free PMC article.
-
Predictors of Outcomes in Gastric Neuroendocrine Tumors: A Retrospective Cohort.GE Port J Gastroenterol. 2023 Jul 14;31(4):236-245. doi: 10.1159/000530684. eCollection 2024 Aug. GE Port J Gastroenterol. 2023. PMID: 39022301 Free PMC article.
References
-
- Scherübl H, Cadiot G, Jensen RT, Rösch T, Stölzel U, Klöppel G. Neuroendocrine tumors of the stomach (gastric carcinoids) are on the rise: small tumors, small problems? Endoscopy. 2010;42:664–671. - PubMed
-
- Ellis L, Shale MJ, Coleman MP. Carcinoid tumors of the gastrointestinal tract: trends in incidence in England since 1971. Am J Gastroenterol. 2010;105:2563–2569. - PubMed
-
- Gastrointestinal Pathology Study Group of Korean Society of Pathologists, Cho MY, Kim JM, Sohn JH, Kim MJ, Kim KM, Kim WH, Kim H, Kook MC, Park DY, Lee JH, Chang H, Jung ES, Kim HK, Jin SY, Choi JH, Gu MJ, Kim S, Kang MS, Cho CH, Park MI, Kang YK, Kim YW, Yoon SO, Bae HI, Joo M, Moon WS, Kang DY, Chang SJ. Current Trends of the Incidence and Pathological Diagnosis of Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs) in Korea 2000-2009: Multicenter Study. Cancer Res Treat. 2012;44:157–165. - PMC - PubMed
-
- Niederle MB, Hackl M, Kaserer K, Niederle B. Gastroenteropancreatic neuroendocrine tumours: the current incidence and staging based on the WHO and European Neuroendocrine Tumour Society classification: an analysis based on prospectively collected parameters. Endocr Relat Cancer. 2010;17:909–918. - PubMed
LinkOut - more resources
Full Text Sources