Evidence map›Paper›PMID 39760880›Full record

ArticleJournal of the National Cancer Institute2025

Adolescents and young adults with germline CDH1 variants and the risk of overtreatment.

Amber F Gallanis, Cassidy Bowden, Rachael Lopez, Grace-Ann Fasaye, David Lang, Jill Rothschild, M Constanza Camargo, Jonathan M Hernandez, Anjali Rai, Theo Heller and 2 more

Abstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Observational
  3. Article
  4. Review
  5. 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

12 authors.

Amber F GallanisCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0003-0194-5375
Cassidy BowdenCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-6746-6142
Rachael LopezClinical Center Nutrition Department, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-5165-5125
Grace-Ann FasayeGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-0478-846X
David LangDepartment of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, United States.ORCID 0009-0005-9386-1161
Jill RothschildDepartment of Pediatrics, National Institutes of Health Clinical Center, Bethesda, MD 20892, United States.
M Constanza CamargoDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-1065-2198
Jonathan M HernandezCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.
Anjali RaiNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-8343-4132
Theo HellerNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-2643-6289
Andrew M BlakelyCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-5013-3851
Jeremy L DavisCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, United States.ORCID 0000-0002-6334-6936

Funding

DLH FoundationIntramural Research ProgramNCI NIH HHSNIH HHSStomach for Cancer, Inc.Stupid Strong Charitable Foundation
6 · The paper itself

Abstract

backgroundAdolescents and young adults (AYA) with germline CDH1 variants are at risk of overtreatment when precancer lesions are detected with endoscopic screening. We characterize diffuse-type gastric cancer prevalence and survival in AYA managed with prophylactic total gastrectomy (PTG) or endoscopic surveillance.

methodsProspective cohort study of 188 individuals aged 39 and younger enrolled from January 27, 2017, to May 1, 2023. Clinicopathological data, prevalence of early gastric signet ring cell (SRC) lesions, advanced gastric cancer diagnoses, and cancer-specific survival were measured.

resultsAmong 188 AYA patients, 104 chose surveillance and 67 pursued PTG for management of elevated gastric cancer risk. AYA who enrolled early in the study period and had SRC lesions detected on preoperative endoscopy were more likely to elect for PTG compared with surveillance. SRC lesions were detected on preoperative endoscopy in 48% of patients who subsequently had PTG, and yet nearly all (93%, 62/67) had multifocal SRC (pT1aN0) on final pathology. Median age at enrollment (30 vs 31 years, P = .21), biological sex (P = .17), and median number of family members with gastric cancer (3 vs 4, P = .14) were not different between groups. No patients under surveillance developed advanced cancer or developed cancer recurrence after PTG with a median follow-up of 2.5 years (IQR = 1.6-4.0) from initial endoscopy.

conclusionsCancer-specific outcomes were not different in AYA who harbored SRC and were managed with surveillance or PTG. Lack of cancer-specific deaths and low prevalence of advanced gastric cancer underscore the risk of overtreatment of SRC lesions and suggest that active surveillance is warranted.

Indexed as

Antigens, CDCadherinsCarcinoma, Signet Ring CellGerm-Line MutationStomach NeoplasmsAdolescentAdultFemaleGastrectomyHumansMalePrevalenceProspective StudiesYoung AdultAntigens, CDCadherinsCDH1 protein, human

Identifiers

PMID39760880
PMCPMC12058253

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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.