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Diagnosing Nonfunctional Pancreatic NETs in MEN1: The Evidence Base
In multiple endocrine neoplasia type 1 (MEN1), nonfunctional pancreatic neuroendocrine tumors (NF-pNETs) are the most frequently diagnosed NETs and a leading cause of MEN1-related death. The high prevalence and malignant potential of NF-pNETs outline the need for an evidence-based screening program,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Endocrine Society
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125714/ https://www.ncbi.nlm.nih.gov/pubmed/30202829 http://dx.doi.org/10.1210/js.2018-00087 |
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author | van Treijen, Mark J C van Beek, Dirk-Jan van Leeuwaarde, Rachel S Vriens, Menno R Valk, Gerlof D |
author_facet | van Treijen, Mark J C van Beek, Dirk-Jan van Leeuwaarde, Rachel S Vriens, Menno R Valk, Gerlof D |
author_sort | van Treijen, Mark J C |
collection | PubMed |
description | In multiple endocrine neoplasia type 1 (MEN1), nonfunctional pancreatic neuroendocrine tumors (NF-pNETs) are the most frequently diagnosed NETs and a leading cause of MEN1-related death. The high prevalence and malignant potential of NF-pNETs outline the need for an evidence-based screening program, as early diagnosis and timely intervention could reduce morbidity and mortality. Controversies exist regarding the value of several diagnostic tests. This systematic review aims to evaluate current literature and amplify an up-to-date evidence-based approach to NF-pNET diagnosis in MEN1. Three databases were systematically searched on the diagnostic value of biomarkers and imaging modalities. Twenty-seven studies were included and critically appraised (modified Quality Assessment of Diagnostic Accuracy Studies). Another 12 studies, providing data on age-related penetrance and tumor growth, were included to assess the optimal frequency and timing of screening. Based on current literature, biomarkers should no longer play a role in the diagnostic process for NF-pNETs, as accuracies are too low. Studies evaluating the diagnostic value of imaging modalities are heterogeneous with varying risks of bias. For the detection of NF-pNETs, endoscopic ultrasound (EUS) has the highest sensitivity. A combined strategy of EUS and MRI seems to be the most useful. Gallium 68 octreotate-DOTA positron emission tomography-CT could be added if NF-pNETs are diagnosed to identify metastasis. Reported growth rates were generally low, and two distinct phenotypes were observed. Surveillance programs should focus on and be adapted to the presence of substantial growth in NF-pNETs. The optimal age to start screening must yet be determined, as insufficient evidence for an evidence-based recommendation was available. |
format | Online Article Text |
id | pubmed-6125714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-61257142018-09-10 Diagnosing Nonfunctional Pancreatic NETs in MEN1: The Evidence Base van Treijen, Mark J C van Beek, Dirk-Jan van Leeuwaarde, Rachel S Vriens, Menno R Valk, Gerlof D J Endocr Soc Mini-Reviews In multiple endocrine neoplasia type 1 (MEN1), nonfunctional pancreatic neuroendocrine tumors (NF-pNETs) are the most frequently diagnosed NETs and a leading cause of MEN1-related death. The high prevalence and malignant potential of NF-pNETs outline the need for an evidence-based screening program, as early diagnosis and timely intervention could reduce morbidity and mortality. Controversies exist regarding the value of several diagnostic tests. This systematic review aims to evaluate current literature and amplify an up-to-date evidence-based approach to NF-pNET diagnosis in MEN1. Three databases were systematically searched on the diagnostic value of biomarkers and imaging modalities. Twenty-seven studies were included and critically appraised (modified Quality Assessment of Diagnostic Accuracy Studies). Another 12 studies, providing data on age-related penetrance and tumor growth, were included to assess the optimal frequency and timing of screening. Based on current literature, biomarkers should no longer play a role in the diagnostic process for NF-pNETs, as accuracies are too low. Studies evaluating the diagnostic value of imaging modalities are heterogeneous with varying risks of bias. For the detection of NF-pNETs, endoscopic ultrasound (EUS) has the highest sensitivity. A combined strategy of EUS and MRI seems to be the most useful. Gallium 68 octreotate-DOTA positron emission tomography-CT could be added if NF-pNETs are diagnosed to identify metastasis. Reported growth rates were generally low, and two distinct phenotypes were observed. Surveillance programs should focus on and be adapted to the presence of substantial growth in NF-pNETs. The optimal age to start screening must yet be determined, as insufficient evidence for an evidence-based recommendation was available. Endocrine Society 2018-07-31 /pmc/articles/PMC6125714/ /pubmed/30202829 http://dx.doi.org/10.1210/js.2018-00087 Text en Copyright © 2018 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Mini-Reviews van Treijen, Mark J C van Beek, Dirk-Jan van Leeuwaarde, Rachel S Vriens, Menno R Valk, Gerlof D Diagnosing Nonfunctional Pancreatic NETs in MEN1: The Evidence Base |
title | Diagnosing Nonfunctional Pancreatic NETs in MEN1: The Evidence Base |
title_full | Diagnosing Nonfunctional Pancreatic NETs in MEN1: The Evidence Base |
title_fullStr | Diagnosing Nonfunctional Pancreatic NETs in MEN1: The Evidence Base |
title_full_unstemmed | Diagnosing Nonfunctional Pancreatic NETs in MEN1: The Evidence Base |
title_short | Diagnosing Nonfunctional Pancreatic NETs in MEN1: The Evidence Base |
title_sort | diagnosing nonfunctional pancreatic nets in men1: the evidence base |
topic | Mini-Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125714/ https://www.ncbi.nlm.nih.gov/pubmed/30202829 http://dx.doi.org/10.1210/js.2018-00087 |
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