Mixed Neuroendocrine Non-Neuroendocrine Neoplasms: A Systematic Review of a Controversial and Underestimated Diagnosis

Mixed neuroendocrine non-neuroendocrine neoplasms (MiNENs) represent a rare diagnosis of the gastro-entero-pancreatic tract. Evidence from the current literature regarding their epidemiology, biology, and management is of variable quality and conflicting. Based on available data, the MiNEN has an ag...

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Main Authors: Melissa Frizziero, Bipasha Chakrabarty, Bence Nagy, Angela Lamarca, Richard A. Hubner, Juan W. Valle, Mairéad G. McNamara
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/9/1/273
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spelling doaj-caec99c77731462abf7913f83124c85a2020-11-25T01:45:51ZengMDPI AGJournal of Clinical Medicine2077-03832020-01-019127310.3390/jcm9010273jcm9010273Mixed Neuroendocrine Non-Neuroendocrine Neoplasms: A Systematic Review of a Controversial and Underestimated DiagnosisMelissa Frizziero0Bipasha Chakrabarty1Bence Nagy2Angela Lamarca3Richard A. Hubner4Juan W. Valle5Mairéad G. McNamara6Department of Medical Oncology, The Christie NHS Foundation Trust, 550 Wilmslow Road, Manchester M20 4BX, UKDepartment of Pathology, The Christie NHS Foundation Trust, 550 Wilmslow Road, Manchester M20 4BX, UKDepartment of Medical Oncology, The Christie NHS Foundation Trust, 550 Wilmslow Road, Manchester M20 4BX, UKDepartment of Medical Oncology, The Christie NHS Foundation Trust, 550 Wilmslow Road, Manchester M20 4BX, UKDepartment of Medical Oncology, The Christie NHS Foundation Trust, 550 Wilmslow Road, Manchester M20 4BX, UKDepartment of Medical Oncology, The Christie NHS Foundation Trust, 550 Wilmslow Road, Manchester M20 4BX, UKDepartment of Medical Oncology, The Christie NHS Foundation Trust, 550 Wilmslow Road, Manchester M20 4BX, UKMixed neuroendocrine non-neuroendocrine neoplasms (MiNENs) represent a rare diagnosis of the gastro-entero-pancreatic tract. Evidence from the current literature regarding their epidemiology, biology, and management is of variable quality and conflicting. Based on available data, the MiNEN has an aggressive biological behaviour, mostly driven by its (often high-grade) neuroendocrine component, and a dismal prognosis. In most cases, the non-neuroendocrine component is of adenocarcinoma histology. Due to limitations in diagnostic methods and poor awareness within the scientific community, the incidence of MiNENs may be underestimated. In the absence of data from clinical trials, MiNENs are commonly treated according to the standard of care for pure neuroendocrine carcinomas or adenocarcinomas from the same sites of origin, based on the assumption of a biological similarity to their pure counterparts. However, little is known about the molecular aberrations of MiNENs, and their pathogenesis remains controversial; molecular/genetic studies conducted so far point towards a common monoclonal origin of the two components. In addition, mutations in tumour-associated genes, including <i>TP53</i>, <i>BRAF,</i> and <i>KRAS</i>, and microsatellite instability have emerged as potential drivers of MiNENs. This systematic review (91 full manuscripts or abstracts in English language) summarises the current reported literature on clinical, pathological, survival, and molecular/genetic data on MiNENs.https://www.mdpi.com/2077-0383/9/1/273mixed non-neuroendocrine neuroendocrine neoplasmsminensmixed adeno-neuroendocrine carcinomamanec2017 who classification2019 who classification
collection DOAJ
language English
format Article
sources DOAJ
author Melissa Frizziero
Bipasha Chakrabarty
Bence Nagy
Angela Lamarca
Richard A. Hubner
Juan W. Valle
Mairéad G. McNamara
spellingShingle Melissa Frizziero
Bipasha Chakrabarty
Bence Nagy
Angela Lamarca
Richard A. Hubner
Juan W. Valle
Mairéad G. McNamara
Mixed Neuroendocrine Non-Neuroendocrine Neoplasms: A Systematic Review of a Controversial and Underestimated Diagnosis
Journal of Clinical Medicine
mixed non-neuroendocrine neuroendocrine neoplasms
minens
mixed adeno-neuroendocrine carcinoma
manec
2017 who classification
2019 who classification
author_facet Melissa Frizziero
Bipasha Chakrabarty
Bence Nagy
Angela Lamarca
Richard A. Hubner
Juan W. Valle
Mairéad G. McNamara
author_sort Melissa Frizziero
title Mixed Neuroendocrine Non-Neuroendocrine Neoplasms: A Systematic Review of a Controversial and Underestimated Diagnosis
title_short Mixed Neuroendocrine Non-Neuroendocrine Neoplasms: A Systematic Review of a Controversial and Underestimated Diagnosis
title_full Mixed Neuroendocrine Non-Neuroendocrine Neoplasms: A Systematic Review of a Controversial and Underestimated Diagnosis
title_fullStr Mixed Neuroendocrine Non-Neuroendocrine Neoplasms: A Systematic Review of a Controversial and Underestimated Diagnosis
title_full_unstemmed Mixed Neuroendocrine Non-Neuroendocrine Neoplasms: A Systematic Review of a Controversial and Underestimated Diagnosis
title_sort mixed neuroendocrine non-neuroendocrine neoplasms: a systematic review of a controversial and underestimated diagnosis
publisher MDPI AG
series Journal of Clinical Medicine
issn 2077-0383
publishDate 2020-01-01
description Mixed neuroendocrine non-neuroendocrine neoplasms (MiNENs) represent a rare diagnosis of the gastro-entero-pancreatic tract. Evidence from the current literature regarding their epidemiology, biology, and management is of variable quality and conflicting. Based on available data, the MiNEN has an aggressive biological behaviour, mostly driven by its (often high-grade) neuroendocrine component, and a dismal prognosis. In most cases, the non-neuroendocrine component is of adenocarcinoma histology. Due to limitations in diagnostic methods and poor awareness within the scientific community, the incidence of MiNENs may be underestimated. In the absence of data from clinical trials, MiNENs are commonly treated according to the standard of care for pure neuroendocrine carcinomas or adenocarcinomas from the same sites of origin, based on the assumption of a biological similarity to their pure counterparts. However, little is known about the molecular aberrations of MiNENs, and their pathogenesis remains controversial; molecular/genetic studies conducted so far point towards a common monoclonal origin of the two components. In addition, mutations in tumour-associated genes, including <i>TP53</i>, <i>BRAF,</i> and <i>KRAS</i>, and microsatellite instability have emerged as potential drivers of MiNENs. This systematic review (91 full manuscripts or abstracts in English language) summarises the current reported literature on clinical, pathological, survival, and molecular/genetic data on MiNENs.
topic mixed non-neuroendocrine neuroendocrine neoplasms
minens
mixed adeno-neuroendocrine carcinoma
manec
2017 who classification
2019 who classification
url https://www.mdpi.com/2077-0383/9/1/273
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