Neuroendocrine Neoplasms of the Small Bowel and Pancreas

The traditionally promulgated perspectives of neuroendocrine neoplasms (NEN) as rare, indolent tumours are blunt and have been outdated for the last 2 decades. Clear increments in their incidence over the past decades render them increasingly clinically relevant, and at initial diagnosis many presen...

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Published inNeuroendocrinology Vol. 110; no. 6; p. 444
Main Authors Clift, Ashley Kieran, Kidd, Mark, Bodei, Lisa, Toumpanakis, Christos, Baum, Richard P, Oberg, Kjell, Modlin, Irvin M, Frilling, Andrea
Format Journal Article
LanguageEnglish
Published Switzerland 01.05.2020
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ISSN1423-0194
DOI10.1159/000503721

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Abstract The traditionally promulgated perspectives of neuroendocrine neoplasms (NEN) as rare, indolent tumours are blunt and have been outdated for the last 2 decades. Clear increments in their incidence over the past decades render them increasingly clinically relevant, and at initial diagnosis many present with nodal and/or distant metastases (notably hepatic). The molecular pathogenesis of these tumours is increasingly yet incompletely understood. Those arising from the small bowel (SB) or pancreas typically occur sporadically; the latter may occur within the context of hereditary tumour predisposition syndromes. NENs can also be associated with endocrinopathy of hormonal hypersecretion. Tangible advances in the development of novel biomarkers, functional imaging modalities and therapy are especially applicable to this sub-set of tumours. The management of SB and pancreatic neuroendocrine tumours (NET) may be challenging, and often comprises a multidisciplinary approach wherein surgical, medical, interventional radiological and radiotherapeutic modalities are implemented. This review provides a comprehensive overview of the epidemiology, pathophysiology, diagnosis and treatment of SB and pancreatic NETs. Moreover, we provide an outlook of the future in these tumour types which will include the development of precision oncology frameworks for individualised therapy, multi-analyte predictive biomarkers, artificial intelligence-derived clinical decision support tools and elucidation of the role of the microbiome in NEN development and clinical behaviour.
AbstractList The traditionally promulgated perspectives of neuroendocrine neoplasms (NEN) as rare, indolent tumours are blunt and have been outdated for the last 2 decades. Clear increments in their incidence over the past decades render them increasingly clinically relevant, and at initial diagnosis many present with nodal and/or distant metastases (notably hepatic). The molecular pathogenesis of these tumours is increasingly yet incompletely understood. Those arising from the small bowel (SB) or pancreas typically occur sporadically; the latter may occur within the context of hereditary tumour predisposition syndromes. NENs can also be associated with endocrinopathy of hormonal hypersecretion. Tangible advances in the development of novel biomarkers, functional imaging modalities and therapy are especially applicable to this sub-set of tumours. The management of SB and pancreatic neuroendocrine tumours (NET) may be challenging, and often comprises a multidisciplinary approach wherein surgical, medical, interventional radiological and radiotherapeutic modalities are implemented. This review provides a comprehensive overview of the epidemiology, pathophysiology, diagnosis and treatment of SB and pancreatic NETs. Moreover, we provide an outlook of the future in these tumour types which will include the development of precision oncology frameworks for individualised therapy, multi-analyte predictive biomarkers, artificial intelligence-derived clinical decision support tools and elucidation of the role of the microbiome in NEN development and clinical behaviour.
Author Bodei, Lisa
Frilling, Andrea
Oberg, Kjell
Modlin, Irvin M
Toumpanakis, Christos
Kidd, Mark
Clift, Ashley Kieran
Baum, Richard P
Author_xml – sequence: 1
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  surname: Clift
  fullname: Clift, Ashley Kieran
  organization: Department of Surgery and Cancer, Imperial College London, London, United Kingdom
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  givenname: Mark
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  fullname: Kidd, Mark
  organization: Wren Laboratories, Branford, Connecticut, USA
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  givenname: Lisa
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  fullname: Bodei, Lisa
  organization: Department of Nuclear Medicine, Memorial Sloan Kettering Cancer Centre, New York, New York, USA
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  givenname: Christos
  surname: Toumpanakis
  fullname: Toumpanakis, Christos
  organization: Centre for Gastroenterology/Neuroendocrine Tumour Unit, Royal Free Hospital, London, United Kingdom
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  givenname: Richard P
  surname: Baum
  fullname: Baum, Richard P
  organization: Theranostics Centre for Molecular Radiotherapy and Precision Oncology, Zentralklinik, Bad Berka, Germany
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  givenname: Kjell
  surname: Oberg
  fullname: Oberg, Kjell
  organization: Department of Endocrine Oncology, Uppsala University, Uppsala, Sweden
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  givenname: Irvin M
  surname: Modlin
  fullname: Modlin, Irvin M
  organization: Yale University School of Medicine, New Haven, Connecticut, USA
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  givenname: Andrea
  surname: Frilling
  fullname: Frilling, Andrea
  email: a.frilling@imperial.ac.uk
  organization: Department of Surgery and Cancer, Imperial College London, London, United Kingdom, a.frilling@imperial.ac.uk
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Issue 6
Keywords Neuroendocrine neoplasm
Neuroendocrine tumour
Pancreas
Small intestine
Language English
License 2019 S. Karger AG, Basel.
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Snippet The traditionally promulgated perspectives of neuroendocrine neoplasms (NEN) as rare, indolent tumours are blunt and have been outdated for the last 2 decades....
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StartPage 444
SubjectTerms Humans
Intestinal Neoplasms - diagnosis
Intestinal Neoplasms - genetics
Intestinal Neoplasms - pathology
Intestinal Neoplasms - therapy
Neuroendocrine Tumors - diagnosis
Neuroendocrine Tumors - genetics
Neuroendocrine Tumors - pathology
Neuroendocrine Tumors - therapy
Pancreatic Neoplasms - diagnosis
Pancreatic Neoplasms - genetics
Pancreatic Neoplasms - pathology
Pancreatic Neoplasms - therapy
Title Neuroendocrine Neoplasms of the Small Bowel and Pancreas
URI https://www.ncbi.nlm.nih.gov/pubmed/31557758
Volume 110
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