Evidence map›Paper›PMID 42225074›Full record

ArticleEndoscopy2026

Aberrant p53 expression, a stronger risk factor for neoplastic progression in Barrett's esophagus than confirmed low grade dysplasia: a large multicenter prospective cohort study.

Pauline A Zellenrath, Nanda Provoost, Jeliena C M Jansen, Nina van Gerwen, Michael Doukas, Pieter Jan F de Jonge, Arjun D Koch, Judith Honing, Manon C W Spaander, Probar Study Group

Abstract readMulticenter Study
In one paragraph

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

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

10 authors.

Pauline A ZellenrathDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Nanda ProvoostDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Jeliena C M JansenDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Nina van GerwenDepartment of Biostatistics, Erasmus University Medical Center, Rotterdam, The Netherlands.
Michael DoukasDepartment of Pathology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Pieter Jan F de JongeDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Arjun D KochDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Judith HoningDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Manon C W SpaanderDepartment of Gastroenterology and Hepatology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Probar Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLow grade dysplasia (LGD) diagnosed on multiple occasions is considered the strongest risk factor for neoplastic progression in patients with Barrett's esophagus (BE); however, recent studies have shown that aberrant p53 expression may be a more powerful risk factor for progression. This study aimed to compare the association between aberrant p53 expression versus LGD diagnosed on two or more occasions and neoplastic progression risk.

methodsPatients with a BE segment length ≥ 2 cm were included in a multicenter prospective cohort. p53 expression was determined by immunohistochemistry staining. Neoplastic progression was defined as development of high grade dysplasia (HGD) or esophageal adenocarcinoma (EAC). Multivariable Cox regression analyses were used to determine the association between selected variables and neoplastic progression risk.

results960 patients (median age 62; 73 % men) were included. During a median (interquartile range) follow-up of 6.3 (3.5-11.9) years, 81 patients (8 %) developed HGD/EAC. p53 expression was aberrant in 24 % of patients, and was strongly associated with an increased risk of progression (hazard ratio [HR] 20.0, 95 %CI 10.0-40.0). In contrast, LGD on multiple occasions was not similarly associated (HR 0.84, 95 %CI 0.47-1.53), after adjustment for age, sex, and segment length. Progression-free survival was better in patients with normal versus aberrant p53 expression, regardless of the histopathological diagnosis (

conclusionsAberrant p53 expression is strongly associated with an increased neoplastic progression risk in BE patients, regardless of the histopathological findings. It may therefore be a better parameter than confirmed LGD on multiple occasions to identify patients who might benefit from ablation therapy.

Indexed as

AdenocarcinomaBarrett EsophagusEsophageal NeoplasmsPrecancerous ConditionsTumor Suppressor Protein p53AgedCohort StudiesDisease ProgressionFemaleHumansImmunohistochemistryMaleMiddle AgedProspective StudiesRisk FactorsTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID42225074
PMCPMC13498430

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