Evidence map›Paper›PMID 39335195›Full record

ArticleCancers2024

Risk of Esophageal and Gastric Cancer in Patients with Type 2 Diabetes Receiving Glucagon-like Peptide-1 Receptor Agonists (GLP-1 RAs): A National Analysis.

Mark Ayoub, Rafi Aibani, Tiana Dodd, Muhammed Ceesay, Muhammad Bhinder, Carol Faris, Nisar Amin, Ebubekir Daglilar

Abstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 4 pooled it
–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

13 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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  5. Article
  6. Metabolic Modulation in Cancer Care: The Potential Role of Glucagon-Like Peptide-1 Receptor Agonists.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
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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

8 authors.

Mark AyoubDepartment of Internal Medicine, Charleston Area Medical Center, West Virginia University, Charleston, WV 25304, USA.ORCID 0009-0002-6518-3971
Rafi AibaniDepartment of Internal Medicine, Charleston Area Medical Center, West Virginia University, Charleston, WV 25304, USA.ORCID 0000-0002-3222-9454
Tiana DoddDepartment of Internal Medicine, Charleston Area Medical Center, West Virginia University, Charleston, WV 25304, USA.
Muhammed CeesayDepartment of Internal Medicine, Charleston Area Medical Center, West Virginia University, Charleston, WV 25304, USA.
Muhammad BhinderDepartment of Internal Medicine, Charleston Area Medical Center, West Virginia University, Charleston, WV 25304, USA.
Carol FarisDepartment of Internal Medicine, Bayonne Medical Center, Bayonne, NJ 07002, USA.
Nisar AminDepartment of Internal Medicine, Charleston Area Medical Center, West Virginia University, Charleston, WV 25304, USA.
Ebubekir DaglilarDivision of Gastroenterology and Hepatology, Charleston Area Medical Center, West Virginia University, Charleston, WV 25304, USA.ORCID 0000-0003-0622-1704

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGlucagon-like peptide-1 receptor agonists (GLP-1 RAs) are becoming more popular in managing type 2 diabetes mellitus (T2DM). Concerns linger over potential links to malignancies like pancreatic and thyroid cancers, requiring more research to clarify their safety profiles. Additionally, evidence suggests GLP-1 RAs may lower colorectal and pancreatic cancer risk, especially in obese and overweight individuals, indicating a protective effect beyond weight loss. Current studies leave a gap in comprehensively understanding cancer risks associated with GLP-1 RAs, which prompts further research to enhance our understanding of their overall safety.

methodsWe queried the US Collaborative Network (63 health care organizations) of the TriNetX research database. Patients with T2DM were identified and divided into two cohorts: patients on GLP-1 RAs and patients not on GLP-1 RAs. We excluded tobacco use and alcohol use disorders, obese patients with a body mass index (BMI) of >25 kg/m

resultsA total of 2,748,431 patients with T2DM were identified. Of those, 6% (

conclusionThe use of GLP-1 RAs in patients with T2DM does not significantly increase the risk of gastric or esophageal cancer. This finding supports the continued use of GLP-1 analogues as a therapeutic option in managing T2DM, considering their well-established benefits and low risk of complications. Based on the study results, these medications may even have a protective effect against these malignancies.

Indexed as

diabetesesophageal cancergastric cancergeneticGLP-1 receptor agonists

Identifiers

PMID39335195
PMCPMC11430483

What OpenQuestion holds

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Registered trials

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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.