Evidence map›Paper›PMID 32467348›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2020

Comparison of Tissue-Based Molecular Markers in Younger versus Older Patients with Colorectal Neoplasia.

Paul J Limburg, Douglas W Mahoney, David A Ahlquist, Hatim T Allawi, Scott C Johnson, Michael Kaiser, Viatcheslav E Katerov, Sandra Statz, Rondell P Graham, Patrick H Foote and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2020. 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
0.5field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Molecular genetics of early-onset colorectal cancer.World journal of biological chemistry · 2023
    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

14 authors at 2 institutions in 1 country.

Paul J LimburgDepartment of Medicine, Mayo Clinic, Rochester, Minnesota. limburg.paul@mayo.edu.
Douglas W MahoneyDivision of Biomedical Statistics & Informatics, Mayo Clinic, Rochester, Minnesota.
David A AhlquistDepartment of Medicine, Mayo Clinic, Rochester, Minnesota.
Hatim T AllawiExact Sciences Corporation, Madison, Wisconsin.
Scott C JohnsonExact Sciences Corporation, Madison, Wisconsin.
Michael KaiserExact Sciences Corporation, Madison, Wisconsin.
Viatcheslav E KaterovExact Sciences Corporation, Madison, Wisconsin.
Sandra StatzExact Sciences Corporation, Madison, Wisconsin.
Rondell P GrahamDivision of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-8686-4867
Patrick H FooteDepartment of Medicine, Mayo Clinic, Rochester, Minnesota.
Karen A DoeringDepartment of Medicine, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-4769-5175
Kelli N BurgerDivision of Biomedical Statistics & Informatics, Mayo Clinic, Rochester, Minnesota.
Graham P LidgardExact Sciences Corporation, Madison, Wisconsin.
John B KisielDepartment of Medicine, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-3840-5324
Mayo Clinic · USExact Sciences (United States) · US

Funding

Multi-site Gastrointestinal Cancer Detection by Stool DNA MethylationR37CA214679 · NCI · MAYO CLINIC ROCHESTER · PI KISIEL, JOHN · 2018 to 2024
$2.8M
NCI NIH HHS R37 CA214679
6 · The paper itself

Abstract

backgroundEmerging colorectal cancer trends demonstrate increased incidence and mortality in younger populations, prompting consideration of average-risk colorectal cancer screening initiation at age 45 versus 50 years. However, screening test performance characteristics in adults 45-49 years have been minimally described. To inform the biologic rationale for multi-target stool DNA (mt-sDNA) screening in younger patients, we analyzed and compared tissue levels of methylation (

methodsWithin 40-44, 45-49, and 50-64 year age groups, archived colorectal tissue specimens were identified for 211 sporadic colorectal cancer cases, 123 advanced precancerous lesions (APLs; adenomas >1 cm, high-grade dysplasia, ≥25% villous morphology, or sessile serrated polyp; 45-49 and 50-64 age groups only), and 204 histologically normal controls. Following DNA extraction,

resultsNone of the molecular marker concentrations were significantly associated with age (

conclusionsOverall, these findings support the potential for earlier onset of average-risk colorectal cancer screening with the mt-sDNA assay. IMPACT: These novel data address an identified knowledge gap and strengthen the biologic basis for earlier-onset, average-risk screening with the mt-sDNA assay.

Indexed as

Age FactorsColorectal NeoplasmsEarly Detection of CancerFemaleHumansMaleMiddle Aged

Identifiers

PMID32467348
PMCPMC10964290
OpenAlexW3030534615

What OpenQuestion holds

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LicenceTDM
Read underepoch 390

Registered trials

None linked

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.