Evidence map›Paper›PMID 41495008›Full record

ArticleThe oncologist2026

Age- and sex-based differences in the genomic profiles of patients with gastrointestinal and pancreatic neuroendocrine neoplasms.

Shuning Li, Lisa Liu, Nishant Gandhi, Alex Farrell, Emil Lou, Heloisa Soares, Bassel Nazha, Jeffrey Swensen, Matthew Oberley, Mark G Evans and 2 more

Abstract read
In one paragraph

Article in The oncologist, 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.

Shuning LiFox Chase Cancer Center, Temple University Health System, Philadelphia, PA 19111, United States.
Lisa LiuFox Chase Cancer Center, Temple University Health System, Philadelphia, PA 19111, United States.
Nishant GandhiCaris Life Sciences, Phoenix, AZ 85040, United States.
Alex FarrellCaris Life Sciences, Phoenix, AZ 85040, United States.
Emil LouMasonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, United States.ORCID 0000-0002-1607-1386
Heloisa SoaresHuntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, United States.
Bassel NazhaWinship Cancer Institute, Emory University, Atlanta, GA 30322, United States.
Jeffrey SwensenCaris Life Sciences, Phoenix, AZ 85040, United States.
Matthew OberleyCaris Life Sciences, Phoenix, AZ 85040, United States.ORCID 0000-0001-6419-2513
Mark G EvansCaris Life Sciences, Phoenix, AZ 85040, United States.
Pamela KunzSmilow Cancer Hospital/Yale Cancer Center, Yale University, North Haven, CT 06510, United States.
Namrata VijayvergiaFox Chase Cancer Center, Temple University Health System, Philadelphia, PA 19111, United States.ORCID 0000-0001-6469-4759

Funding

National Cancer Institute of the National Institutes of Health P30CA006927
6 · The paper itself

Abstract

purposeAge and sex are known to influence outcomes in neuroendocrine neoplasms (NENs), yet their molecular determinants remain poorly defined. We queried a real-world dataset of gastrointestinal (GI) tract and pancreatic (P) NENs and characterized their clinical, molecular, and immune profiles.

methodsOne thousand nine hundred thirty-five cases (GI: n = 1431, P: n = 504) of NENs were analyzed using Next Generation or Whole Exome Sequencing of DNA, and 1211/1935 cases (GI: n = 917, P: n = 294) underwent Whole Transcriptome Sequencing. We compared the molecular and immune profile with respect to age and sex.

resultsOlder age at diagnosis was associated with worse survival in both GI- and P-NENs. In patients with GI-NENs, there was decreased survival in males compared to females. In GI-NENs, TP53, RB1, FAT1, and KMT2D mutations, as well as immune checkpoint gene (ICG) expressions of LAG3, CD80, and HAVCR2 and M1 macrophages increased with increasing age while APC mutations and M2 macrophages decreased with increasing age. In P-NENs, TP53, RB1, KRAS, and SMAD4 mutations and CD4+ T cells increased with increasing age while MUTYH and NTHL1 mutations and M2 macrophages decreased with increasing age. In GI-NENs, TP53, FBXW7, and TERT (promoter) mutations and genomic loss of heterozygosity (gLOH) were increased in males. In P-NENs, PIK3CA mutations and dMMR/MSI-H were increased in females.

conclusionOur study queries one of the largest datasets of GI- and P-NENs to date and highlights distinct age- and sex-specific molecular and immune profiles. Given the exploratory nature of these analyses and borderline significance, these results remain hypothesis-generating, providing an initial framework for future validation studies.

Indexed as

Gastrointestinal NeoplasmsNeuroendocrine TumorsPancreatic NeoplasmsAdultAgedAged, 80 and overAge FactorsFemaleGenomicsHumansMaleMiddle AgedSex Factorsage stratificationGI-NENimmune landscapemolecular profilingneuroendocrine neoplasmsP-NENsex differences

Identifiers

PMID41495008
PMCPMC12923116

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LicenceCC BY-NC
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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.