Evidence map›Paper›PMID 38873722›Full record

ArticleJAMA2024

Germline CDH1 Variants and Lifetime Cancer Risk.

Carrie E Ryan, Grace-Ann Fasaye, Amber F Gallanis, Lauren A Gamble, Paul H McClelland, Anna Duemler, Sarah G Samaranayake, Andrew M Blakely, Christine M Drogan, Kerry Kingham and 9 more

Abstract readMulticenter Study
In one paragraph

Article in JAMA, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

  1. Trial
  2. Review
  3. Breast-Ovarian Hereditary Cancer Syndrome: BeyondCurrent oncology (Toronto, Ont.) · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Germline whole-exome sequencing identifies CTNND1 as a candidate gene for hereditary gastric cancer in a large Brazilian cohort.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2026
    Article
  8. Article
  9. Predictors of early cancer burden inEClinicalMedicine · 2026
    Article
  10. Review
  11. Article
  12. Cancer Diagnoses in Patients With Cleft Lip and/or Palate: Increased Childhood Cancer Occurrence.The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association · 2026
    Article
  13. Article
  14. [Next-Generation Sequencing-Based Detection of Gene Mutations and Its Association With Clinicopathological Features in Gastric Cancer].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Article
  15. Article
  16. Article
  17. Review
  18. AME case reports · 2026
    Article
  19. Review
  20. 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

19 authors.

Carrie E RyanCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Grace-Ann FasayeGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Amber F GallanisCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Lauren A GambleCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Paul H McClellandCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Anna DuemlerGenetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Sarah G SamaranayakeCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Andrew M BlakelyCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Christine M DroganSection of Gastroenterology, Hepatology and Nutrition, University of Chicago, Chicago, Illinois.
Kerry KinghamCancer Genetics and Genomics, Stanford University, Stanford, California.
Devanshi PatelCenter for Cancer Risk Assessment, Massachusetts General Hospital, Boston.
Linda Rodgers-FoucheCenter for Cancer Risk Assessment, Massachusetts General Hospital, Boston.
Ava SiegelDivision of Gastroenterology, Massachusetts General Hospital, Boston.
Sonia S KupferSection of Gastroenterology, Hepatology and Nutrition, University of Chicago, Chicago, Illinois.
James M FordDepartment of Medicine, Division of Oncology, Stanford University School of Medicine, Stanford, California.
Daniel C ChungCenter for Cancer Risk Assessment, Massachusetts General Hospital, Boston.
James G DowtyCentre for Epidemiology and Biostatistics, University of Melbourne, Melbourne, Victoria, Australia.
Joshua SampsonDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Jeremy L DavisCenter for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Funding

Surgical Oncology Program Training ProgramZIEBC012097 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI BLAKELY, ANDREW · 2022 to 2025
$17.3M
FITting noninvasive testing into Lynch syndrome colorectal cancer surveillance: a multicenter, prospective trialR01CA287257 · NCI · UNIVERSITY OF CHICAGO · PI Fay Kastrinos, Sonia Kupfer · 2024 to 2026
$3.4M
Colonic responses to vitamin D and aspirin in African- and European-AmericansR01CA220329 · NCI · UNIVERSITY OF CHICAGO · PI KUPFER, SONIA · 2018 to 2022
$1.9M
CRYSTAL STRUCTURES OF PURINE AND PYRIMIDINE ANALOGUESR01CA012159 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BUGG, CHARLES E. · 1985 to 1987
–
NCI NIH HHS R01 CA220329NCI NIH HHS R01 CA287257NCI NIH HHS ZIA BC012159
6 · The paper itself

Abstract

Importance: Approximately 1% to 3% of gastric cancers and 5% of lobular breast cancers are hereditary. Loss of function CDH1 gene variants are the most common gene variants associated with hereditary diffuse gastric cancer and lobular breast cancer. Previously, the lifetime risk of gastric cancer was estimated to be approximately 25% to 83% and for breast cancer it was estimated to be approximately 39% to 55% in individuals with loss of function CDH1 gene variants. Objective: To describe gastric and breast cancer risk estimates for individuals with CDH1 variants. Design, Setting, and Participants: Multicenter, retrospective cohort and modeling study of 213 families from North America with a CDH1 pathogenic or likely pathogenic (P/LP) variant in 1 or more family members conducted between January 2021 and August 2022. Main Outcomes and Measures: Hazard ratios (HRs), defined as risk in variant carriers relative to noncarriers, were estimated for each cancer type and used to calculate cumulative risks and risks per decade of life up to age 80 years. Results: A total of 7323 individuals from 213 families were studied, including 883 with a CDH1 P/LP variant (median proband age, 53 years [IQR, 42-62]; 4% Asian; 4% Hispanic; 85% non-Hispanic White; 50% female). In individuals with a CDH1 P/LP variant, the prevalence of gastric cancer was 13.9% (123/883) and the prevalence of breast cancer among female carriers was 26.3% (144/547). The estimated HR for advanced gastric cancer was 33.5 (95% CI, 9.8-112) at age 30 years and 3.5 (95% CI, 0.4-30.3) at age 70 years. The lifetime cumulative risk of advanced gastric cancer in male and female carriers was 10.3% (95% CI, 6%-23.6%) and 6.5% (95% CI, 3.8%-15.1%), respectively. Gastric cancer risk estimates based on family history indicated that a carrier with 3 affected first-degree relatives had a penetrance of approximately 38% (95% CI, 25%-64%). The HR for breast cancer among female carriers was 5.7 (95% CI, 2.5-13.2) at age 30 years and 3.9 (95% CI, 1.1-13.7) at age 70 years. The lifetime cumulative risk of breast cancer among female carriers was 36.8% (95% CI, 25.7%-62.9%). Conclusions and Relevance: Among families from North America with germline CDH1 P/LP variants, the cumulative risk of gastric cancer was 7% to 10%, which was lower than previously described, and the cumulative risk of breast cancer among female carriers was 37%, which was similar to prior estimates. These findings inform current management of individuals with germline CDH1 variants.

Indexed as

Antigens, CDBreast NeoplasmsCadherinsGenetic Predisposition to DiseaseGerm-Line MutationStomach NeoplasmsAdultAgedFemaleHeterozygoteHumansLoss of Function MutationMaleMiddle AgedPenetranceProspective StudiesAntigens, CDCadherinsCDH1 protein, human

Identifiers

PMID38873722
PMCPMC11372503

What OpenQuestion holds

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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.