Evidence map›Paper›PMID 38224564›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2024

Next-generation Multi-target Stool DNA Panel Accurately Detects Colorectal Cancer and Advanced Precancerous Lesions.

Zubin D Gagrat, Martin Krockenberger, Abhik Bhattacharya, Bridget Z Gagrat, Christine M Leduc, Michael B Matter, Keith D Fourrier, Douglas W Mahoney, David K Edwards V, Graham P Lidgard and 4 more

2 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 4% 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.

NCT04144738 completednot on this map

Clinical Validation of An Optimized Multi-Target Stool DNA (Mt-sDNA 2.0) Test, for Colorectal Cancer Screening "BLUE-C"

TypeobservationalSponsorExact Sciences CorporationRan2019 to 2023Enrolled26,758ConditionsColorectal CancerArmsmt-sDNA 2.0 screening test, FIT test, Colonoscopy
NCT06342440 recruitingnot on this map

A Liquid Biopsy Assay For The Non-Invasive Early Detection of Advanced Adenomas and Colorectal Cancer

TypeobservationalSponsorCity of Hope Medical CenterRan2020 to 2028Enrolled2,000ConditionsColorectal Cancer, Colorectal Neoplasms, Colorectal Polyp, Colorectal AdenocarcinomaArmsDENEB
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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  10. Early detection of pancreatic cancer: Study design and analytical considerations in biomarker discovery and early phase validation studies.Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] · 2024
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 1 country.

Zubin D GagratExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0008-3314-5384
Martin KrockenbergerExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0000-9201-4984
Abhik BhattacharyaExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0006-8022-1576
Bridget Z GagratExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0001-4593-8989
Christine M LeducExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0000-1025-386X
Michael B MatterExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0002-0893-0846
Keith D FourrierExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0001-5350-5817
Douglas W MahoneyDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0001-5144-0645
David K Edwards VExact Sciences Corporation, Madison, Wisconsin.ORCID 0000-0003-2708-9562
Graham P LidgardExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0009-0225-4251
Paul J LimburgExact Sciences Corporation, Madison, Wisconsin.ORCID 0000-0002-2428-5675
Scott C JohnsonExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0009-0103-6498
Michael J DomanicoExact Sciences Corporation, Madison, Wisconsin.ORCID 0009-0006-1780-1279
John B KisielDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-3840-5324
Exact Sciences (United States) · USMayo Clinic · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The multi-target stool DNA (mt-sDNA) test screens for colorectal cancer by analyzing DNA methylation/mutation and hemoglobin markers to algorithmically derive a qualitative result. A new panel of highly discriminant candidate methylated DNA markers (MDM) was recently developed. Performance of the novel MDM panel, with hemoglobin, was evaluated in a simulated screening population using archived stool samples weighted to early-stage colorectal cancer and prospectively collected advanced precancerous lesions (APL). Marker selection study (MSS) and separate preliminary independent verification studies (VS) were conducted utilizing samples from multi-center, case-control studies. Sample processing included targeted MDM capture, bisulfite conversion, and MDM quantitation. Fecal hemoglobin was quantified using ELISA. Samples were stratified into 75%/25% training-testing sets; model outcomes were cross-validated 1,000 times. All laboratory operators were blinded. The MSS included 232 cases (120 colorectal cancer/112 APLs) and 490 controls. The VS featured 210 cases (112 colorectal cancer/98 APLs) and 567 controls; APLs were 86.7% adenomas and 13.3% sessile serrated lesions (SSL). Average age was 65.5 (cases) and 63.2 (controls) years. Mean sensitivity in the VS from cross-validation was 95.2% for colorectal cancer and 57.2% for APLs, with specificities of 89.8% (no CRC/APLs) and 92.4% (no neoplasia). Subgroup analyses showed colorectal cancer sensitivities of 93.4% (stage I) and 94.2% (stage II). APL sensitivity was 82.9% for high-grade dysplasia, 73.4% for villous lesions, 49.8% for tubular lesions, and 30.2% for SSLs. These data support high sensitivity and specificity for a next-generation mt-sDNA test panel. Further evaluation of assay performance will be characterized in a prospective, multi-center clinical validation study (NCT04144738). PREVENTION RELEVANCE: This study highlights performance of the next-generation mt-sDNA test, which exhibits high sensitivity and specificity for detecting colorectal cancer and APLs. This noninvasive option has potential to increase screening participation and clinical outcomes. A multi-center, clinical validation trial is underway. See related commentary by Bresalier, p. 93.

Indexed as

Colorectal NeoplasmsPrecancerous ConditionsAgedDNAEarly Detection of CancerFecesHemoglobinsHumansMiddle AgedProspective StudiesSensitivity and SpecificityDNAHemoglobins

Identifiers

PMID38224564
PMCPMC10911803
OpenAlexW4390875107

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.