Literature DB >> 28664309

Management of gastric neuro-endocrine tumours in a large French national cohort (GTE).

Sylvain Manfredi1, Thomas Walter2, Eric Baudin3, Romain Coriat4, Philippe Ruszniewski5, Thierry Lecomte6, Anne-Pascale Laurenty7, Bernard Goichot8, Vincent Rohmer9, Guillaume Roquin10, Oana-Zvetlana Cojocarasu11, Catherine Lombard-Bohas2, Côme Lepage12, Jeff Morcet13, Guillaume Cadiot14.   

Abstract

INTRODUCTION: Gastric neuro-endocrine tumours are rare. European guidelines for the management of neuro-endocrine tumours have been published in 2012. The aim of our survey was to study the management of gastric neuro-endocrine tumours registered in the national cohort. A prospective national cohort registers the Neuro-endocrine tumours in France since January 2003 (GTE network). We reviewed all the individual medical reports of gastric neuro-endocrine tumours in order to collect data on treatment.
RESULTS: One hundred and ninety seven gastric neuro-endocrine tumours diagnosed between 1964 and 2013 in 20 centres were registered. For 181 cases data were considered complete for our survey. Eighty four tumours were type 1 (46.4%); five types 2 (2.8%); 52 types 3 (28.7%) and 40 types 4 (22.1%). Types 1 and 2 were first endoscopically managed in 93 and 60% of cases, respectively, whereas surgery was first done in 45 and 42%, respectively, of types 3 and 4. Systemic treatment, chemotherapy and/or somatostatin analogue, was first administered exclusively for types 3 and 4. Near 3% of types 1 and 40% of types 2 received at a time somatostatin analogue treatment. Five-year survival rates were 98.3, 100, 63.2 and 31.8% for types 1, 2, 3 and 4, respectively.
CONCLUSION: The great majority of gastric neuro-endocrine tumours registered in this national cohort are treated in accordance with the current guidelines. The survival rates we reported must be interpreted with caution, because this cohort registered preferentially selected patients eligible for treatment. The registration of all the gastric neuro-endocrine tumours, in particular type 1 considered as benign and type 4 not eligible for specific anti-cancer treatment must be encouraged.

Entities:  

Keywords:  Cohort; Gastric neuro-endocrine tumour; Survival; Treatment

Mesh:

Year:  2017        PMID: 28664309     DOI: 10.1007/s12020-017-1355-9

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.633


  32 in total

1.  Treatment of type II gastric carcinoid tumors with somatostatin analogues.

Authors:  P Tomassetti; M Migliori; G C Caletti; P Fusaroli; R Corinaldesi; L Gullo
Journal:  N Engl J Med       Date:  2000-08-24       Impact factor: 91.245

2.  Survival from malignant digestive endocrine tumors in England and Wales: a population-based study.

Authors:  Côme Lepage; Bernard Rachet; Michel Philippe Coleman
Journal:  Gastroenterology       Date:  2007-01-05       Impact factor: 22.682

Review 3.  Management of gastric and duodenal neuroendocrine tumors.

Authors:  Yuichi Sato; Satoru Hashimoto; Ken-Ichi Mizuno; Manabu Takeuchi; Shuji Terai
Journal:  World J Gastroenterol       Date:  2016-08-14       Impact factor: 5.742

4.  A proposed staging system for gastric carcinoid tumors based on an analysis of 1,543 patients.

Authors:  Christine S Landry; Guy Brock; Charles R Scoggins; Kelly M McMasters; Robert C G Martin
Journal:  Ann Surg Oncol       Date:  2008-10-24       Impact factor: 5.344

5.  Placebo-controlled, double-blind, prospective, randomized study on the effect of octreotide LAR in the control of tumor growth in patients with metastatic neuroendocrine midgut tumors: a report from the PROMID Study Group.

Authors:  Anja Rinke; Hans-Helge Müller; Carmen Schade-Brittinger; Klaus-Jochen Klose; Peter Barth; Matthias Wied; Christina Mayer; Behnaz Aminossadati; Ulrich-Frank Pape; Michael Bläker; Jan Harder; Christian Arnold; Thomas Gress; Rudolf Arnold
Journal:  J Clin Oncol       Date:  2009-08-24       Impact factor: 44.544

6.  Lanreotide in metastatic enteropancreatic neuroendocrine tumors.

Authors:  Martyn E Caplin; Marianne Pavel; Jarosław B Ćwikła; Alexandria T Phan; Markus Raderer; Eva Sedláčková; Guillaume Cadiot; Edward M Wolin; Jaume Capdevila; Lucy Wall; Guido Rindi; Alison Langley; Séverine Martinez; Joëlle Blumberg; Philippe Ruszniewski
Journal:  N Engl J Med       Date:  2014-07-17       Impact factor: 91.245

Review 7.  Multiple endocrine neoplasia type 1 and Zollinger-Ellison syndrome: a prospective study of 107 cases and comparison with 1009 cases from the literature.

Authors:  Fathia Gibril; Michael Schumann; Andrea Pace; Robert T Jensen
Journal:  Medicine (Baltimore)       Date:  2004-01       Impact factor: 1.889

8.  Gastric endocrine tumors type I: treatment with long-acting somatostatin analogs.

Authors:  D Campana; F Nori; R Pezzilli; L Piscitelli; D Santini; E Brocchi; R Corinaldesi; P Tomassetti
Journal:  Endocr Relat Cancer       Date:  2008-03       Impact factor: 5.678

9.  Long-term follow-up of a large series of patients with type 1 gastric carcinoid tumors: data from a multicenter study.

Authors:  Dimitrios Thomas; Apostolos V Tsolakis; Simona Grozinsky-Glasberg; Merav Fraenkel; Krystallenia Alexandraki; Stavros Sougioultzis; David J Gross; Gregory Kaltsas
Journal:  Eur J Endocrinol       Date:  2013-01-17       Impact factor: 6.664

10.  Defining surgical indications for type I gastric carcinoid tumor.

Authors:  Rebecca A Gladdy; Vivian E Strong; Daniel Coit; Peter J Allen; Hans Gerdes; Jinru Shia; David S Klimstra; Murray F Brennan; Laura H Tang
Journal:  Ann Surg Oncol       Date:  2009-11       Impact factor: 5.344

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  2 in total

1.  Gastric neuroendocrine neoplasms type 1: A systematic review and meta-analysis.

Authors:  Apostolos V Tsolakis; Athanasia Ragkousi; Miroslav Vujasinovic; Gregory Kaltsas; Kosmas Daskalakis
Journal:  World J Gastroenterol       Date:  2019-09-21       Impact factor: 5.742

2.  Endoscopic techniques for diagnosis and treatment of gastro-entero-pancreatic neuroendocrine neoplasms: Where we are.

Authors:  Roberta Elisa Rossi; Alessandra Elvevi; Camilla Gallo; Andrea Palermo; Pietro Invernizzi; Sara Massironi
Journal:  World J Gastroenterol       Date:  2022-07-14       Impact factor: 5.374

  2 in total

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