Evidence map›Paper›PMID 42606162›Full record

ArticleCancer2026

Practical considerations for the use of incretin mimetics in patients with neuroendocrine neoplasms: An expert consensus statement.

Udhayvir S Grewal, Po H Ear, Mohamad B Sonbol, Andrew M Bellizzi, Johannes Hofland, Joakim Crona, Joseph S Dillon, Jennifer A Chan, James R Howe, Jonathan Strosberg and 2 more

Abstract readConsensus Statement
In one paragraph

Article in Cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Udhayvir S GrewalDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, Georgia, USA.
Po H EarDepartment of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, Georgia, USA.
Mohamad B SonbolMayo Clinic Comprehensive Cancer Center, Scottsdale, Arizona, USA.ORCID https://orcid.org/0000-0002-6931-242X
Andrew M BellizziDepartment of Pathology, Columbia University Vagelos College of Physicians and Surgeons, New York, New York, USA.
Johannes HoflandDepartment of Internal Medicine, ENETS Center of Excellence, Section of Endocrinology, Erasmus MC Cancer Center, Erasmus MC, Rotterdam, the Netherlands.
Joakim CronaDepartment of Medical Sciences, Uppsala Universitet, Uppsala, Sweden.
Joseph S DillonDivision of Endocrinology and Metabolism, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
Jennifer A ChanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
James R HoweDepartment of Surgery, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
Jonathan StrosbergDepartment of Medical Oncology, Moffitt Cancer Institute, Tampa, Florida, USA.
Simron SinghDepartment of Medical Oncology, Sunnybrook Health Sciences Center/Odette Cancer Center, Toronto, Ontario, Canada.
Thorvardur R HalfdanarsonDepartment of Oncology, Mayo Clinic Comprehensive Cancer Center, Rochester, Minnesota, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Incretin-based therapies, including glucagon-like peptide-1 receptor agonists (GLP-1RA) and dual incretin agonists, are increasingly used for the management of diabetes, obesity, and cardiometabolic disease. Although their systemic benefits are well established, uncertainty remains regarding their safety in patients with neuroendocrine neoplasms (NENs), a biologically heterogeneous group of tumors with diverse molecular profiles. Preclinical studies suggest that GLP-1 receptor activation may promote tumor growth in select receptor-expressing models, although receptor expression varies widely across NEN subtypes and is often absent in common tumors such as ileal neuroendocrine tumors. Population-level and retrospective clinical data have not demonstrated a consistent increase in oncologic risk but are limited by methodological constraints. In this expert consensus statement, the authors synthesize current evidence and provide a practical framework for the use of incretin mimetics in patients with NENs. The authors emphasize individualized risk assessment, shared decision-making, and multi-disciplinary collaboration, balancing potential but unquantified oncologic risks against substantial cardiometabolic benefits. Until prospective data are available, careful patient selection, dose optimization, and close clinical and radiologic surveillance remain essential to guide safe and effective use of these agents in this population.

Indexed as

IncretinsNeuroendocrine TumorsGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsHumansRisk AssessmentGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsIncretinsGLP‐1incretin mimeticsneuroendocrine neoplasmsneuroendocrine tumorssemaglutidetirzepatide

Identifiers

PMID42606162
PMCPMC13479761

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.