Evidence map›Paper›PMID 40985860›Full record

ArticleInternational journal of cancer2026

The diagnostic potential of urinary volatile organic compounds for colorectal neoplasia in Lynch syndrome-A prospective longitudinal study.

Elsa L S A van Liere, Dewkoemar Ramsoekh, Trenton K Stewart, Emma Daulton, Maarten A J M Jacobs, Evelien Dekker, Sofie Bosch, James A Covington, Tim G J de Meij, Nanne K H de Boer

Abstract read
In one paragraph

Article in International journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Elsa L S A van LiereDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-4826-3443
Dewkoemar RamsoekhDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Trenton K StewartSchool of Engineering, University of Warwick, Coventry, UK.
Emma DaultonSchool of Engineering, University of Warwick, Coventry, UK.
Maarten A J M JacobsDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Evelien DekkerDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Sofie BoschDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
James A CovingtonSchool of Engineering, University of Warwick, Coventry, UK.
Tim G J de MeijAmsterdam Gastroenterology Endocrinology Metabolism Research Institute, Amsterdam, The Netherlands.
Nanne K H de BoerDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, The Netherlands.

Funding

Maag Lever Darm Stichting WO 19-05Vaillant Fonds
6 · The paper itself

Abstract

Post-colonoscopy colorectal cancer (CRC) rates and colonoscopy burden are considerable in Lynch syndrome. Urinary volatile organic compounds (VOCs) have shown promise as a patient-friendly alternative to faecal biomarkers for colorectal neoplasia detection. To evaluate the potential of urinary VOCs to guide optimal colonoscopy intervals in Lynch syndrome, we performed an exploratory prospective longitudinal study in urine collected by individuals with Lynch syndrome before and after colonoscopy. VOC patterns were analysed by field asymmetric ion mobility spectrometry (FAIMS) and gas chromatography-ion mobility spectrometry (GC-IMS) followed by machine learning algorithms. Gas chromatography time-of-flight mass spectrometry analysed the abundance of individual VOCs. Among 98 included individuals (median 51y, 58% female), 34 had relevant neoplasia at colonoscopy, including 28 non-advanced adenomas, 3 advanced adenomas, 2 CRCs, and 1 advanced serrated lesion. For GC-IMS, the respective sensitivity and negative predictive value for relevant neoplasia were 65% and 79% (70% specificity); for FAIMS, 74% and 75% (42% specificity). VOC patterns differed before and after polypectomy (AUC 0.84), while after polypectomy they resembled those of individuals without neoplasia (AUC 0.52). Non-advanced adenoma presence was associated with increased urinary abundance of decanoic acid (fatty acid). Diagnostic accuracy of urinary VOC patterns for relevant neoplasia was influenced by sample size and external confounders and was lower than for faecal VOC patterns among 50 individuals who had also collected faeces. Urinary VOCs hold promise as non-invasive biomarkers for postponing colonoscopy and for follow-up after polypectomy in Lynch syndrome, though large validation studies are needed that also assess stability and accuracy compared to faecal VOCs.

Indexed as

Biomarkers, TumorColorectal NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisVolatile Organic CompoundsAdultAgedColonoscopyFemaleGas Chromatography-Mass SpectrometryHumansIon Mobility SpectrometryLongitudinal StudiesMaleMiddle AgedProspective StudiesBiomarkers, TumorVolatile Organic Compoundsbiomarkerscolorectal cancerLynch syndromesurveillancevolatile organic compounds

Identifiers

PMID40985860
PMCPMC12588553

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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.