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Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer
Author(s) -
Bond Ashley,
Greenwood Rosemary,
Lewis Stephen,
Corfe Bernard,
Sarkar Sanchoy,
O'Toole Paul,
Rooney Paul,
Burkitt Michael,
Hold Georgina,
Probert Chris
Publication year - 2019
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/apt.15140
Subject(s) - colorectal cancer , biomarker , medicine , colonoscopy , gastroenterology , logistic regression , feces , cancer , area under the curve , chemistry , biology , microbiology and biotechnology , biochemistry
Summary Background Colorectal cancer remains a leading cause of mortality and morbidity. The UK Bowel Cancer Screening Programme (BCSP) has demonstrated that detection of colorectal cancer at an earlier stage and identification of advanced pre‐malignant adenomas reduces mortality and morbidity. Aim To assess the utility of volatile organic compounds as a biomarker for colorectal neoplasia. Methods Faeces were collected from symptomatic patients and people participating in the UK BCSP , prior to colonoscopy. Headspace extraction followed by gas chromatography mass spectrometry was performed on faeces to identify volatile organic compounds. Logistic regression modelling and 10‐fold cross‐validation were used to test potential biomarkers. Results One hundred and thirty‐seven participants were included (mean age 64 years [range 22‐85], 54% were male): 60 had no neoplasia, 56 had adenomatous polyp(s) and 21 had adenocarcinoma. Propan‐2‐ol was significantly more abundant in the cancer samples ( P < 0.0001, q = 0.004) with an area under ROC ( AUROC ) curve of 0.76. When combined with 3‐methylbutanoic acid the AUROC curve was 0.82, sensitivity 87.9% (95% CI 0.87‐0.99) and specificity 84.6% (95% CI 0.65‐1.0). Logistic regression analysis using the presence/absence of specific volatile organic compounds, identified a three volatile organic compound panel (propan‐2‐ol, hexan‐2‐one and ethyl 3‐methyl‐ butanoate) to have an AUROC of 0.73, with a person six times more likely to have cancer if all three volatile organic compounds were present ( P < 0.0001). Conclusions Volatile organic compound analysis may have a superior diagnostic ability for the identification of colorectal adenocarcinoma, when compared to other faecal biomarkers, including those currently employed in UK . Clinical trial details: National Research Ethics Service Committee South West ‐ Central Bristol ( REC reference 14/ SW /1162) with R&D approval from University of Liverpool and Broadgreen University Hospital Trust (UoL 001098).