Evidence map›Paper›PMID 35041098›Full record

ArticleAnnals of surgical oncology2022

Clinical Relevance of the Tumor Location-Modified Laurén Classification System for Gastric Cancer in a Western Population.

J L Moore, A R Davies, A Santaolalla, M Van Hemelrijck, N Maisey, J Lagergren, J A Gossage, M Kelly, C R Baker, Guy’s and St. Thomas’ Esophago-gastric Research Group

Open access · hybridAbstract read
In one paragraph

Article in Annals of surgical oncology, 2022. 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
0.8field-weighted citation impact, top 30% of its field
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, 6 citations in OpenAlex.

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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

10 authors at 1 institution in 2 countries.

J L MooreDepartment of Upper Gastrointestinal and General Surgery, St. Thomas' Hospital, London, UK. Jonathan.moore13@NHS.net.
A R DaviesDepartment of Upper Gastrointestinal and General Surgery, St. Thomas' Hospital, London, UK.
A SantaolallaSchool of Cancer and Pharmaceutical Sciences, King's College, London, UK.
M Van HemelrijckSchool of Cancer and Pharmaceutical Sciences, King's College, London, UK.
N MaiseyDepartment of Medical Oncology, St. Thomas' Hospital, London, UK.
J LagergrenDepartment of Upper Gastrointestinal and General Surgery, St. Thomas' Hospital, London, UK.
J A GossageDepartment of Upper Gastrointestinal and General Surgery, St. Thomas' Hospital, London, UK.
M KellyDepartment of Upper Gastrointestinal and General Surgery, St. Thomas' Hospital, London, UK.
C R BakerDepartment of Upper Gastrointestinal and General Surgery, St. Thomas' Hospital, London, UK.
Guy’s and St. Thomas’ Esophago-gastric Research Group
King's College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Tumor Location-Modified Laurén Classification (MLC) system combines Laurén histologic subtype and anatomic tumor location. It divides gastric tumors into proximal non-diffuse (PND), distal non-diffuse (DND), and diffuse (D) types. The optimum classification of patients with Laurén mixed tumors in this system is not clear due to its grouping with both diffuse and non-diffuse types in previous studies. The clinical relevance of the MLC in a Western population has not been examined.

methodsA cohort study investigated 404 patients who underwent gastrectomy for gastric adenocarcinoma between 2005 and 2020. The classification of Laurén mixed tumors was evaluated using receiver operating characteristic (ROC) curve analysis and comparison of clinicopathologic characteristics (chi-square). Survival analysis was performed using multivariable Cox regression.

resultsThe ROC curve analysis demonstrated a slightly higher area under the curve value for predicting survival when Laurén mixed tumors were grouped with intestinal-type rather than diffuse-type tumors (0.58 vs 0.57). Survival, tumor recurrence, and resection margin positivity in mixed tumors also was more similar to intestinal type. Distal non-diffuse tumors had the best 5-year survival (DND 64.7 % vs PND 56.1 % vs diffuse 45.1 %; p = 0.006) and were least likely to have recurrence (DND 27.0 % vs PND 34.3 % vs diffuse 48.3 %; p = 0.001). Multivariable analysis demonstrated that MLC was an independent prognostic factor for survival (PND: hazard ratio [HR], 1.64; 95 % confidence interval [CI], 1.16-2.32 vs diffuse: HR, 2.20; 95 % CI, 1.56-3.09)

conclusionsThe MLC was an independent prognostic marker in this Western cohort of patients with gastric adenocarcinoma. The patients with PND and D tumors had worse survival than those with DND tumors.

Indexed as

AdenocarcinomaStomach NeoplasmsCohort StudiesGastrectomyHumansNeoplasm StagingPrognosisRetrospective Studies

Identifiers

PMID35041098
PMCPMC9072452
OpenAlexW4206023564

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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.