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promulgated perspectives of neuroendocrine neoplasms (NEN) as rare, indolent tumours are blunt and have been outdated for the last 2 decades.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 in | Neuroendocrinology Vol. 110; no. 6; p. 444 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
01.05.2020
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Subjects | |
Online Access | Get more information |
ISSN | 1423-0194 |
DOI | 10.1159/000503721 |
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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promulgated perspectives of neuroendocrine neoplasms (NEN) as rare, indolent tumours are blunt and have been outdated for the last 2 decades.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. |
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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 givenname: Ashley Kieran surname: Clift fullname: Clift, Ashley Kieran organization: Department of Surgery and Cancer, Imperial College London, London, United Kingdom – sequence: 2 givenname: Mark surname: Kidd fullname: Kidd, Mark organization: Wren Laboratories, Branford, Connecticut, USA – sequence: 3 givenname: Lisa surname: Bodei fullname: Bodei, Lisa organization: Department of Nuclear Medicine, Memorial Sloan Kettering Cancer Centre, New York, New York, USA – sequence: 4 givenname: Christos surname: Toumpanakis fullname: Toumpanakis, Christos organization: Centre for Gastroenterology/Neuroendocrine Tumour Unit, Royal Free Hospital, London, United Kingdom – sequence: 5 givenname: Richard P surname: Baum fullname: Baum, Richard P organization: Theranostics Centre for Molecular Radiotherapy and Precision Oncology, Zentralklinik, Bad Berka, Germany – sequence: 6 givenname: Kjell surname: Oberg fullname: Oberg, Kjell organization: Department of Endocrine Oncology, Uppsala University, Uppsala, Sweden – sequence: 7 givenname: Irvin M surname: Modlin fullname: Modlin, Irvin M organization: Yale University School of Medicine, New Haven, Connecticut, USA – sequence: 8 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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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 |
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