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Epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria

BACKGROUND: The lack of uniform criteria for coding of gastroenteropancreatic neuroendocrine neoplasia (GEP‐NEN) has hampered previous epidemiological studies. The epidemiology of GEP‐NEN was investigated in this study using currently available criteria. METHODS: All patients diagnosed with GEP‐NEN...

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Autores principales: Sandvik, O. M., Søreide, K., Gudlaugsson, E., Kvaløy, J. T., Søreide, J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061026/
https://www.ncbi.nlm.nih.gov/pubmed/26511392
http://dx.doi.org/10.1002/bjs.10034
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author Sandvik, O. M.
Søreide, K.
Gudlaugsson, E.
Kvaløy, J. T.
Søreide, J. A.
author_facet Sandvik, O. M.
Søreide, K.
Gudlaugsson, E.
Kvaløy, J. T.
Søreide, J. A.
author_sort Sandvik, O. M.
collection PubMed
description BACKGROUND: The lack of uniform criteria for coding of gastroenteropancreatic neuroendocrine neoplasia (GEP‐NEN) has hampered previous epidemiological studies. The epidemiology of GEP‐NEN was investigated in this study using currently available criteria. METHODS: All patients diagnosed with GEP‐NEN between January 2003 and December 2013 in a well defined Norwegian population of approximately 350 000 people were included. Age‐ and sex‐adjusted incidence rates were calculated. The current 2010 World Health Organization criteria, European Neuroendocrine Tumour Society classification and International Union Against Cancer (UICC) classification were used. RESULTS: A total of 204 patients (114 male, 55·9 per cent) were identified. The median age at diagnosis was 61 (range 10–94) years. The annual overall crude incidence was 5·83 per 100 000 inhabitants, with an increasing trend (P = 0·033). The most frequent location was small intestine (60 patients, 29·4 per cent) followed by appendix (48 patients, 23·5 per cent) and pancreas (33 patients, 16·2 per cent). Grade 1 tumours were more common in gastrointestinal (100 patients, 58·5 per cent) than in pancreatic (9 patients, 27 per cent) NEN. According to the UICC classification, 77 patients (37·7 per cent) had stage I, 17 patients (8·3 per cent) stage II, 37 patients (18·1 per cent) stage III and 70 patients (34·3 per cent) had stage IV disease. No patient with stage I disease had grade 3 tumours; advanced tumour grade increased with stage. CONCLUSION: A high crude incidence of GEP‐NEN, at 5·83 per 100 000 inhabitants, was noted together with a significant increasing trend over time.
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spelling pubmed-50610262016-10-19 Epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria Sandvik, O. M. Søreide, K. Gudlaugsson, E. Kvaløy, J. T. Søreide, J. A. Br J Surg Original Articles BACKGROUND: The lack of uniform criteria for coding of gastroenteropancreatic neuroendocrine neoplasia (GEP‐NEN) has hampered previous epidemiological studies. The epidemiology of GEP‐NEN was investigated in this study using currently available criteria. METHODS: All patients diagnosed with GEP‐NEN between January 2003 and December 2013 in a well defined Norwegian population of approximately 350 000 people were included. Age‐ and sex‐adjusted incidence rates were calculated. The current 2010 World Health Organization criteria, European Neuroendocrine Tumour Society classification and International Union Against Cancer (UICC) classification were used. RESULTS: A total of 204 patients (114 male, 55·9 per cent) were identified. The median age at diagnosis was 61 (range 10–94) years. The annual overall crude incidence was 5·83 per 100 000 inhabitants, with an increasing trend (P = 0·033). The most frequent location was small intestine (60 patients, 29·4 per cent) followed by appendix (48 patients, 23·5 per cent) and pancreas (33 patients, 16·2 per cent). Grade 1 tumours were more common in gastrointestinal (100 patients, 58·5 per cent) than in pancreatic (9 patients, 27 per cent) NEN. According to the UICC classification, 77 patients (37·7 per cent) had stage I, 17 patients (8·3 per cent) stage II, 37 patients (18·1 per cent) stage III and 70 patients (34·3 per cent) had stage IV disease. No patient with stage I disease had grade 3 tumours; advanced tumour grade increased with stage. CONCLUSION: A high crude incidence of GEP‐NEN, at 5·83 per 100 000 inhabitants, was noted together with a significant increasing trend over time. John Wiley & Sons, Ltd 2015-10-29 2016-02 /pmc/articles/PMC5061026/ /pubmed/26511392 http://dx.doi.org/10.1002/bjs.10034 Text en © 2015 The Authors. BJS published by John Wiley & Sons Ltd on behalf of BJS Society Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Sandvik, O. M.
Søreide, K.
Gudlaugsson, E.
Kvaløy, J. T.
Søreide, J. A.
Epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria
title Epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria
title_full Epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria
title_fullStr Epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria
title_full_unstemmed Epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria
title_short Epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria
title_sort epidemiology and classification of gastroenteropancreatic neuroendocrine neoplasms using current coding criteria
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061026/
https://www.ncbi.nlm.nih.gov/pubmed/26511392
http://dx.doi.org/10.1002/bjs.10034
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