Evidence map›Paper›PMID 40498571›Full record

ArticleJNCI cancer spectrum2025

Increased colorectal and endometrial cancer rates in a genomically ascertained Lynch syndrome cohort.

Miranda L G Hallquist, Juliann M Savatt, Kristy Diloreto, Alicia Johns, Amie Decker, Cameron Hayes, Melissa A Kelly, Henry Lester Kirchner, Natasha T Strande, Adam H Buchanan

Abstract read
In one paragraph

Article in JNCI cancer spectrum, 2025. 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
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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

10 authors.

Miranda L G HallquistDepartment of Genomic Health, Geisinger, Danville, PA, United States.ORCID 0000-0001-8554-2447
Juliann M SavattDepartment of Genomic Health, Geisinger, Danville, PA, United States.ORCID 0000-0001-6444-1962
Kristy DiloretoDepartment of Genomic Health, Geisinger, Danville, PA, United States.ORCID 0009-0005-9189-6408
Alicia JohnsDepartment of Population Health Sciences, Geisinger, Danville, PA, United States.
Amie DeckerDepartment of Genomic Health, Geisinger, Danville, PA, United States.
Cameron HayesDepartment of Genomic Health, Geisinger, Danville, PA, United States.
Melissa A KellyDepartment of Genomic Health, Geisinger, Danville, PA, United States.ORCID 0000-0003-4708-2261
Henry Lester KirchnerDepartment of Population Health Sciences, Geisinger, Danville, PA, United States.ORCID 0000-0002-2557-6749
Natasha T StrandeDepartment of Developmental Medicine, Geisinger, Danville, PA, United States.ORCID 0000-0001-5148-9772
Adam H BuchananDepartment of Genomic Health, Geisinger, Danville, PA, United States.ORCID 0000-0002-6518-2453

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLynch syndrome (LS) is a hereditary cancer predisposition that increases risk for colorectal, endometrial, and other cancers. Although population-based genomic screening programs identify individuals with LS, clinical presentation in such genomically ascertained populations is unknown.

methodsMyCode is a healthcare system-based biobank that returns clinically actionable genomic screening results to participants, including pathogenic/likely pathogenic (P/LP) variants in LS genes (MLH1, MSH2, MSH6, PMS2). Adult cases (participants with an LS result) and controls (participants without a cancer predisposition variant matched to cases) reported their personal and family cancer histories. Rates of meeting National Comprehensive Cancer Network (NCCN) genetic testing guidelines and rates of colorectal and endometrial cancers in cases, controls, and their family members were calculated and compared.

resultsA total of 175 cases (10 MLH1, 7 MSH2, 83 MSH6, and 75 PMS2) and 169 controls were included. Of case pedigrees, 62/175 (35.4%) met NCCN criteria for LS evaluation. Case pedigrees were more likely (P < .001) to meet criteria than control pedigrees (4/169, 8.35%). Case probands had significantly higher rates of colorectal and endometrial cancer than controls (7.7% vs 2.4%, P = .03 colorectal; 11.5% vs 0%, P < .001 endometrial), as did their relatives (3.1% vs 0.9%, P < .001 colorectal; 2.2% vs 0.5%, P < .001 endometrial).

conclusionsNCCN guidelines missed 65% of cases with P/LP LS variants despite families having higher colorectal and endometrial cancer rates compared with controls. Genomic screening can assist in identifying individuals at risk for LS-related cancers, providing an opportunity to tailor risk management for cancer prevention and early detection.

Indexed as

Colorectal NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisEndometrial NeoplasmsAdultAgedCase-Control StudiesDNA-Binding ProteinsFemaleGenetic Predisposition to DiseaseGenetic TestingHumansMaleMiddle AgedMismatch Repair Endonuclease PMS2MutL Protein Homolog 1MutS Homolog 2 ProteinDNA-Binding ProteinsG-T mismatch-binding proteinMismatch Repair Endonuclease PMS2MLH1 protein, humanMSH2 protein, humanMutL Protein Homolog 1MutS Homolog 2 ProteinPMS2 protein, human

Identifiers

PMID40498571
PMCPMC12288957

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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.