Evidence map›Paper›PMID 42446796›Full record

ArticleAnnals of surgical oncology2026

High Prevalence of Clinical Understaging in Early Gastric Cancer: An Analysis of the NCDB.

Alexandra Adams, Katherine De La Torre Cisneros, Brijesh Rana, Hayavadhan Thuppal, Mariam F Eskander, Brett L Ecker, Miral Sadaria Grandhi, Elizabeth Handorf, Haejin In

Abstract read
In one paragraph

Article in Annals of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Alexandra AdamsDivision of Surgical Oncology, Rutgers Cancer Institute, New Brunswick, NJ, USA.
Katherine De La Torre CisnerosDivision of Surgical Oncology, Rutgers Cancer Institute, New Brunswick, NJ, USA.
Brijesh RanaDivision of Surgical Oncology, Rutgers Cancer Institute, New Brunswick, NJ, USA.
Hayavadhan ThuppalDepartment of Surgery, Montefiore Medical Center, Bronx, NY, USA.
Mariam F EskanderDivision of Surgical Oncology, Rutgers Cancer Institute, New Brunswick, NJ, USA.
Brett L EckerDepartment of Surgery, Northwestern University, Chicago, IL, USA.
Miral Sadaria GrandhiDepartment of Surgery, Endeavor Health, Evanston, IL, USA.
Elizabeth HandorfDepartment of Biostatistics and Epidemiology, Rutgers School of Public Health, Piscataway, NJ, USA.
Haejin InDivision of Surgical Oncology, Rutgers Cancer Institute, New Brunswick, NJ, USA. Haejin.In@rutgers.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to identify the incidence of clinical understaging in early gastric cancer (GC) and to identify variables associated with increased risk of a patient being understaged.

methodsClinical stage I (T1/2 N0) GC patients undergoing oncologic resection without neoadjuvant therapy from 2013 to 2020 were identified in the National Cancer Database (NCDB). Patients found to have a higher stage of cancer on final pathologic review were considered understaged. Clinicopathologic predictors of understaging were identified using multivariable logistic regression. The relationship between identified variables and understaging was modeled using logistic regression with natural cubic splines to allow for a flexible, nonlinear analysis. Cox proportional hazards analysis and Kaplan-Meier curves were used to evaluate survival outcomes.

resultsThe study identified 4370 clinical stage I GC patients, 36% of whom were initially understaged on clinical staging. Tumor size per millimeter increase (OR, 1.05; 95% confidence interval CI 1.04-1.05; p < 0.001), higher grade (moderate: OR, 2.76; 95% CI 1.99-3.84; poor/anaplastic status: OR, 5.99; 95% CI 1.99-3.84, p < 0.001), and non-academic treatment facilities (OR, 1.19; 95% CI 1.03-1.38; p = 0.017) were associated with increased risk of understaging. Spline analysis showed increased risk of understaging based on tumor size. This was compounded when tumor differentiation was considered, such that a tumor measuring 2.5 cm was associated with 16.9%, 31.8%, or 51.6% likelihood of clinical understaging if the tumor was well, moderately, or poorly differentiated, respectively. Understaging was associated with increased mortality (OR, 2.31; 95% CI 2.10-2.95; p < 0.001).

conclusionsMore than one third of clinical stage I GC patients are understaged. Tumor grade and size should be considered at preoperative evaluation of early GC to improve identification of patients at risk for understaging.

Indexed as

GastrectomyStomach NeoplasmsAgedDatabases, FactualFemaleFollow-Up StudiesHumansMaleMiddle AgedNeoplasm StagingPrevalencePrognosisSurvival RateClinical StageGastric CancerOutcomesPathologic StageStaging

Identifiers

PMID42446796
PMCPMC13585805

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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.