Evidence map›Paper›PMID 42022130›Full record

ArticleESMO gastrointestinal oncology2026

Real-world insights into young-onset gastroesophageal adenocarcinoma: an all-Ireland population-based cancer registry analysis.

O Deac, M T Redaniel, J McDevitt, A Brennan, D Fitzpatrick, H G Coleman, R C Turkington, C Donohoe, R Narayanasamy, J A Elliott and 3 more

Abstract read
In one paragraph

Article in ESMO gastrointestinal oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Data resource profile: National Cancer Registry Ireland.ESMO real world data and digital oncology · 2026
    Article
  2. Article
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

13 authors.

O DeacTrinity St James's Cancer Institute, St James's Hospital, Dublin, Ireland.
M T RedanielNational Cancer Registry Ireland, Cork, Ireland.
J McDevittNational Cancer Registry Ireland, Cork, Ireland.
A BrennanNational Cancer Registry Ireland, Cork, Ireland.
D FitzpatrickNorthern Ireland Cancer Registry, Belfast, UK.
H G ColemanNorthern Ireland Cancer Registry, Belfast, UK.
R C TurkingtonCentre for Public Health, School of Medicine, Dentistry and Biomedical Sciences, Queens University Belfast, Belfast, UK.
C DonohoeTrinity St James's Cancer Institute, St James's Hospital, Dublin, Ireland.
R NarayanasamyTrinity St James's Cancer Institute, St James's Hospital, Dublin, Ireland.
J A ElliottTrinity St James's Cancer Institute, St James's Hospital, Dublin, Ireland.
J ReynoldsTrinity St James's Cancer Institute, St James's Hospital, Dublin, Ireland.
J O'SullivanTrinity St James's Cancer Institute, St James's Hospital, Dublin, Ireland.
M A LoweryTrinity St James's Cancer Institute, St James's Hospital, Dublin, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Population-based studies report a rising incidence of young-onset (YO) oesophageal and gastric cancer. We examined clinicopathological features, treatment, and outcomes in YO (18-50 years), midlife-onset (MO, 50-70 years), and late-onset (LO, >70 years) oesophageal and gastric adenocarcinoma. Methods: Population-based data were collected from the National Cancer Registry Ireland (NCRI) and Northern Ireland Cancer Registry (NICR). Incidence trends were determined using Joinpoint regression. Kaplan-Meier curves, log-rank tests, and multivariable Cox regression were used to assess survival differences. Multivariable Cox regression was adjusted for key clinical covariates, and excluded patients with missing covariates. Results: We analysed 21 706 patients diagnosed with oesophageal or gastric adenocarcinoma from 1999 to 2022. YO gastric tumours were more diffuse (YO 26.6% versus MO 13.8% versus LO 10.4%, Conclusion: Oesophageal adenocarcinoma incidence is rising across all age groups, while gastric adenocarcinoma incidence was stable in the YO population and declining in older adults. Despite more advanced and aggressive disease at presentation, YO patients had better overall survival.

Indexed as

gastric adenocarcinomaincidence trendsoesophageal adenocarcinomapopulation-based cancer registrysocioeconomic deprivationyoung-onset

Identifiers

PMID42022130
PMCPMC13098464

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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.