Evidence map›Paper›PMID 40347392›Full record

ArticleEndocrine pathology2025

Clinicopathological Correlates of Hormone Expression-Based Subtypes of Non-Functioning Duodenal/Ampullary Neuroendocrine Tumors: A Multicenter Study of 151 Cases.

Alessandro Vanoli, Nestor Piva, Frediano Socrate Inzani, Federica Grillo, Catherine Klersy, Silvia Uccella, Paola Spaggiari, Luca Albarello, Marco Schiavo Lena, Massimo Milione and 15 more

Abstract readMulticenter Study
In one paragraph

Article in Endocrine pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Concept of neuroendocrine neoplasms of all organs with a focus on grading, subtyping.Virchows Archiv : an international journal of pathology · 2026
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Alessandro VanoliAnatomic Pathology Unit, Department of Molecular Medicine, University of Pavia, Via Carlo Forlanini 16, 27100, Pavia, Italy. alessandro.vanoli@unipv.it.
Nestor PivaAnatomic Pathology Department, Federal University of São Paulo, São Paulo, Brazil.
Frediano Socrate InzaniAnatomic Pathology Unit, Department of Molecular Medicine, University of Pavia, Via Carlo Forlanini 16, 27100, Pavia, Italy.
Federica GrilloAnatomic Pathology, Department of Surgical Sciences and Integrated Diagnostics (DISC), University of Genova, Genova, Italy.
Catherine KlersyBiostatistics & Clinical Trial Center, Research Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Silvia UccellaDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.
Paola SpaggiariDepartment of Pathology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Luca AlbarelloPathology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Marco Schiavo LenaPathology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Massimo MilioneDepartment of Pathology and Laboratory Medicine, First Division of Pathology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Caterina AntoniacomiAnatomic Pathology Unit, Department of Molecular Medicine, University of Pavia, Via Carlo Forlanini 16, 27100, Pavia, Italy.
Anna Caterina MilanettoPancreatic and Digestive Endocrine Surgical Research Group, Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy.
Alessandro ZerbiDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.
Antonio Di SabatinoDepartment of Internal Medicine and Medical Therapeutics, University of Pavia, Pavia, Italy.
Massimo FalconiVita-Salute San Raffaele University, Milan, Italy.
Andrea AnderloniDepartment of Internal Medicine and Medical Therapeutics, University of Pavia, Pavia, Italy.
Paola MattioloDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Verona, Italy.
Claudio LuchiniDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Verona, Italy.
Aldo ScarpaDepartment of Diagnostics and Public Health, Section of Pathology, University and Hospital Trust of Verona, Verona, Italy.
Matteo FassanDepartment of Medicine, Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy.
Paola ParenteUnit of Pathology, Fondazione IRCCS Ospedale Casa Sollievo Della Sofferenza, San Giovanni Rotondo, Foggia, Italy.
Ombretta LuinettiAnatomic Pathology, Fondazione IRCCS San Matteo Hospital, Pavia, Italy.
Guido RindiSection of Anatomic Pathology, Department of Life Sciences and Public Health, Università Cattolica del Sacro Cuore, Rome, Italy.
Marco PaulliAnatomic Pathology Unit, Department of Molecular Medicine, University of Pavia, Via Carlo Forlanini 16, 27100, Pavia, Italy.
Stefano La RosaPathology Unit, Department of Medicine and Technological Innovation, University of Insubria, Varese, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duodenal neuroendocrine tumors (Duo-NETs) may arise in the ampullary and non-ampullary duodenum. Non-functioning Duo-NETs (NF-Duo-NETs), which account for most cases, may express various hormones. Previous studies have suggested that hormone production might be associated with biological aggressiveness. Current treatment protocols are based on functionality, tumor size, and location, but small NF-Duo-NETs may also have metastatic potential. We aimed to investigate whether tumor cell subtyping, based on hormone expression, could provide further insights into NF-Duo-NET biological behavior. We analyzed the clinico-pathological correlates of hormone expression in a multicenter series of 151 NF-Duo-NETs, subdividing tumors into five subtypes: gastrin-producing G-cell NETs (Gas-NETs), somatostatin-producing D-cell NETs (Som-NETs), serotonin-producing enterochromaffin-cell NETs (Ser-NETs), plurihormonal NETs, and gastrin-, somatostatin-, and serotonin-negative NETs (GSSN-NETs). Som-NETs were the most frequent (31%), followed by plurihormonal NETs (26%), Gas-NETs (24%), GSSN-NETs (13%), and Ser-NETs (4%). Som-NETs and GSSN-NETs were more commonly located in the ampullary region and showed significantly larger size, more frequent lymphatic and/or vascular invasion, and higher pT, pN, and American Joint Committee on Cancer (AJCC-9th edition) stages compared to Gas-NETs, which were often (77%) diagnosed at AJCC stage I. Ampullary Som-NETs showed a more invasive and metastatic potential compared to non-ampullary Som-NETs, while, among plurihormonal NETs, the predominantly expressed hormone influenced tumor biological features, with gastrin-predominant NETs showing less invasive potential. At logistic regression, both tumor cell subtype and tumor size were independently associated with aggressiveness (pT3, pN1, or pM1 stage at diagnosis). Hormonal expression profiling may be clinically relevant in NF-Duo-NETs, independently of tumor size.

Indexed as

Ampulla of VaterDuodenal NeoplasmsNeuroendocrine TumorsAdultAgedAged, 80 and overBiomarkers, TumorFemaleGastrinsHumansMaleMiddle AgedYoung AdultBiomarkers, TumorGastrinsCell subtypingGastrinNull-cell tumorsPlurihormonal tumorsSomatostatin

Identifiers

PMID40347392
PMCPMC12065733

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.