Evidence map›Paper›PMID 39629931›Full record

ArticleCancer medicine2024

Differences in Ancestry and Presence of Gastric Precursor Lesions in Individuals With Young- and Average-Onset Gastric Cancer.

Patrick T Magahis, Nicole Cornet, Laura Tang, Kanika Arora, Neha Hingorani, Stephanie King, Arnold J Markowitz, Mark Schattner, Shoji Shimada, Steven B Maron and 10 more

Abstract read
In one paragraph

Article in Cancer medicine, 2024. 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

20 authors.

Patrick T MagahisWeill Cornell Medical College of Cornell University, New York, New York, USA.ORCID 0000-0002-2083-3398
Nicole CornetDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Laura TangDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Kanika AroraDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Neha HingoraniGastroenterology, Hepatology, and Nutrition Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Stephanie KingGastroenterology, Hepatology, and Nutrition Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Arnold J MarkowitzDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Mark SchattnerDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Shoji ShimadaGastric and Mixed Tumor Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Steven B MaronDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Santosha VardhanaDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Melissa LumishGastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Andrea CercekDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Yelena Y JanjigianDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Daniel CoitDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Robin B MendelsohnDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.ORCID 0000-0002-5291-0191
Michael F BergerDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Vivian E StrongDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.
Zsofia K StadlerGastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Monika LaszkowskaDepartment of Medicine, Weill Cornell Medicine, New York, New York, USA.ORCID 0000-0001-6816-3293

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Comparative modeling of gastric cancer health drivers and prevention in the US and globallyU01CA265729 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HUR, CHIN, YEH, JENNIFER M. · 2021 to 2025
$4.1M
A Targeted Approach to the Surveillance of Precursor Lesions for Gastric CancerK08DK125876 · NIDDK · SLOAN-KETTERING INST CAN RESEARCH · PI LASZKOWSKA, MONIKA · 2021 to 2025
$838k
NCI NIH HHS P30 CA008748NCI NIH HHS U01 CA265729NIDDK NIH HHS K08 DK125876
6 · The paper itself

Abstract

backgroundThere has been a paradoxical rise in young-onset gastric cancer (YOGC), defined as gastric cancer (GC) diagnosed before age 50. Precursor lesions may contribute to pathogenesis, though their role in progression to different histologic subtypes is unclear. The impact of self-reported race is also poorly characterized and may be unreliable as a proxy for genetic differences. We aimed to compare differences in histology and genetic ancestry between YOGC and average-onset gastric cancer (AOGC).

methodsThis retrospective cohort included all patients with GC at Memorial Sloan Kettering (MSK) from January 2013 to March 2021. Data on demographics, tumor characteristics, and precursor lesions were collected. Genetic ancestry was inferred from MSK-Integrated Mutation Profiling of Actionable Cancer Targets panel.

resultsOf 1685 individuals with GC, 290 had YOGC. Compared to AOGC, individuals with YOGC tended to be female, Hispanic, foreign-born, and feature diffuse-type histology. YOGC was less likely to have precursor lesions, including intestinal metaplasia (20% vs. 37%, p < 0.01) and dysplasia (4% vs. 14%, p < 0.01). Of 560 patients with ancestry data, 127 had YOGC. Admixed, East Asian, and South Asian ancestries were more likely to present with YOGC while Europeans presented with AOGC. Intestinal metaplasia was enriched among East Asians, maintained when stratifying by histology and GC onset.

conclusionsWe observed YOGC was more common in East and South Asians, and while YOGC may be less likely to develop in the setting of precursor lesions these high-risk states may also be enriched in East Asians. Future research is needed to understand drivers behind such differences and outcome disparities given these individuals may be less amenable to endoscopic interventions.

Indexed as

Age of OnsetPrecancerous ConditionsStomach NeoplasmsAdultAgedFemaleHumansMaleMetaplasiaMiddle AgedRetrospective Studiesancestryprecursor lesionscreeningyoung‐onset gastric cancer

Identifiers

PMID39629931
PMCPMC11615756

What Socratic holds

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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 Socratic graph.