Evidence map›Paper›PMID 40912495›Full record

ArticleGastrointestinal endoscopy2026

Anatomical location of colorectal neoplasia in patients with positive stool test (multitarget stool deoxyribonucleic acid or fecal immunochemical test) results: data from the New Hampshire Colonoscopy Registry.

Joseph C Anderson, William M Hisey, Christina M Robinson, Paul J Limburg, Bonny L Kneedler, Lynn F Butterly

Abstract read
In one paragraph

Article in Gastrointestinal endoscopy, 2026. 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

6 authors.

Joseph C AndersonGeisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA; White River Junction VAMC, White River Junction, Vermont, USA. Electronic address: joseph.anderson@dartmouth.edu.
William M HiseyDepartment of Medicine, Section of Gastroenterology and Hepatology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA; NH Colonoscopy Registry, Lebanon, New Hampshire, USA.
Christina M RobinsonDepartment of Medicine, Section of Gastroenterology and Hepatology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA; NH Colonoscopy Registry, Lebanon, New Hampshire, USA.
Paul J LimburgExact Sciences Corporation, Madison, Wisconsin, USA.
Bonny L KneedlerExact Sciences Corporation, Madison, Wisconsin, USA.
Lynn F ButterlyGeisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA; Department of Medicine, Section of Gastroenterology and Hepatology, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA; NH Colonoscopy Registry, Lebanon, New Hampshire, USA.

Funding

Optimizing colorectal cancer prevention: a multi-disciplinary, population-based investigation of serrated polyps using risk prediction and modelingR01CA243449 · NCI · DARTMOUTH-HITCHCOCK CLINIC · PI AMOS, CHRISTOPHER I., BUTTERLY, LYNN F · 2020 to 2024
$3.0M
NCI NIH HHS R01 CA243449
6 · The paper itself

Abstract

BACKGROUND AND

aimsData comparing the location of polyp yield in patients with positive stool test results can aid screening test selection. We conducted a cross-sectional analysis of New Hampshire Colonoscopy Registry data to compare the location, left versus right side of the colon, of neoplasia detected on colonoscopy after a multitarget stool DNA (mt-sDNA) test or a fecal immunochemical test (FIT), compared with a reference group undergoing colonoscopy without a stool test.

methodsOur outcomes were advanced lesions (adenomas and/or serrated polyps, including cancer), advanced adenomas, or advanced serrated polyps stratified by location. We examined the prevalence of left- versus right-sided lesions across 3 cohorts.

resultsAs compared to colonoscopy (n = 68,645), both FIT+ (n = 584) and mt-sDNA+ (n = 1176) patients had higher proportions of advanced lesions and advanced adenomas on both sides of the colon (P < .001). Mt-sDNA+ patients had significantly higher risks for right-sided advanced serrated polyps (odds ratio [OR], 3.21; 95% confidence interval [CI], 2.67-3.85; colonoscopy [reference]) and right-sided advanced lesions (OR, 3.13; 95% CI, 2.66-3.68; colonoscopy [reference]) as compared to FIT+ (advanced serrated polyps: OR, 1.38; 95% CI, 0.99-1.99 and advanced lesions: OR, 1.84; 95% CI, 1.43-2.37) or colonoscopy (reference). In our main analysis, the colonoscopy-only group had significantly higher odds of each outcome on the right side than the left side; in comparison, the odds for FIT+ and mt-sDNA+ patients were more evenly distributed throughout the colon.

conclusionsOur data suggest that FIT+ tests are associated with higher detection of both right- and left-sided advanced adenomas as compared to colonoscopy without a prior stool test. Furthermore, mt-sDNA+ patients had higher proportions of left- and right-sided advanced adenomas and advanced serrated polyps, particularly on the right side.

Indexed as

AdenomaColonic PolypsColorectal NeoplasmsDNA, NeoplasmFecesOccult BloodAgedColonoscopyCross-Sectional StudiesEarly Detection of CancerFemaleHumansMaleMiddle AgedNew HampshireRegistriesDNA, Neoplasm

Identifiers

PMID40912495
PMCPMC13001995

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