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Colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the HUNT study

BACKGROUND: Colorectal cancer (CRC) is often diagnosed in advanced stages. Circulating tumour DNA (ctDNA) has been proposed as an early diagnostic biomarker. However, as a screening tool, ctDNA has mainly been studied in selected populations at the time of clinical diagnosis. The aim of this study w...

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Autores principales: Brenne, Siv S., Madsen, Poul Henning, Pedersen, Inge Søkilde, Hveem, Kristian, Skorpen, Frank, Krarup, Henrik Bygum, Giskeødegård, Guro F., Laugsand, Eivor A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449868/
https://www.ncbi.nlm.nih.gov/pubmed/37438612
http://dx.doi.org/10.1038/s41416-023-02337-4
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author Brenne, Siv S.
Madsen, Poul Henning
Pedersen, Inge Søkilde
Hveem, Kristian
Skorpen, Frank
Krarup, Henrik Bygum
Giskeødegård, Guro F.
Laugsand, Eivor A.
author_facet Brenne, Siv S.
Madsen, Poul Henning
Pedersen, Inge Søkilde
Hveem, Kristian
Skorpen, Frank
Krarup, Henrik Bygum
Giskeødegård, Guro F.
Laugsand, Eivor A.
author_sort Brenne, Siv S.
collection PubMed
description BACKGROUND: Colorectal cancer (CRC) is often diagnosed in advanced stages. Circulating tumour DNA (ctDNA) has been proposed as an early diagnostic biomarker. However, as a screening tool, ctDNA has mainly been studied in selected populations at the time of clinical diagnosis. The aim of this study was to detect CRC by known ctDNA markers up to 2 years prior to clinical diagnosis. METHODS: In this case–control study, methylated ctDNA markers were detected in plasma samples from 106 healthy controls and 106 individuals diagnosed with CRC within 24 months following participation in The Trøndelag Health Study. RESULTS: The most specific single markers were BMP3, FLI1, IKZF1, SFRP1, SFRP2, NPTX2, SLC8A1 and VIM (specificity >70%). When combining these into a panel, the CRC sensitivity was 43% (95% CI 42.7–43.4) and the CRC specificity was 86% (95% CI 85.7–86.2). The findings were reproduced in an independent validation set of samples. CONCLUSIONS: Detection of known methylated ctDNA markers of CRC is possible up to 2 years prior to the clinical diagnosis in an unselected population resembling the screening setting. This study supports the hypothesis that some patients could be diagnosed earlier, if ctDNA detection was part of the CRC screening programme. [Image: see text]
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spelling pubmed-104498682023-08-26 Colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the HUNT study Brenne, Siv S. Madsen, Poul Henning Pedersen, Inge Søkilde Hveem, Kristian Skorpen, Frank Krarup, Henrik Bygum Giskeødegård, Guro F. Laugsand, Eivor A. Br J Cancer Article BACKGROUND: Colorectal cancer (CRC) is often diagnosed in advanced stages. Circulating tumour DNA (ctDNA) has been proposed as an early diagnostic biomarker. However, as a screening tool, ctDNA has mainly been studied in selected populations at the time of clinical diagnosis. The aim of this study was to detect CRC by known ctDNA markers up to 2 years prior to clinical diagnosis. METHODS: In this case–control study, methylated ctDNA markers were detected in plasma samples from 106 healthy controls and 106 individuals diagnosed with CRC within 24 months following participation in The Trøndelag Health Study. RESULTS: The most specific single markers were BMP3, FLI1, IKZF1, SFRP1, SFRP2, NPTX2, SLC8A1 and VIM (specificity >70%). When combining these into a panel, the CRC sensitivity was 43% (95% CI 42.7–43.4) and the CRC specificity was 86% (95% CI 85.7–86.2). The findings were reproduced in an independent validation set of samples. CONCLUSIONS: Detection of known methylated ctDNA markers of CRC is possible up to 2 years prior to the clinical diagnosis in an unselected population resembling the screening setting. This study supports the hypothesis that some patients could be diagnosed earlier, if ctDNA detection was part of the CRC screening programme. [Image: see text] Nature Publishing Group UK 2023-07-12 2023-09-21 /pmc/articles/PMC10449868/ /pubmed/37438612 http://dx.doi.org/10.1038/s41416-023-02337-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Brenne, Siv S.
Madsen, Poul Henning
Pedersen, Inge Søkilde
Hveem, Kristian
Skorpen, Frank
Krarup, Henrik Bygum
Giskeødegård, Guro F.
Laugsand, Eivor A.
Colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the HUNT study
title Colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the HUNT study
title_full Colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the HUNT study
title_fullStr Colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the HUNT study
title_full_unstemmed Colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the HUNT study
title_short Colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the HUNT study
title_sort colorectal cancer detected by liquid biopsy 2 years prior to clinical diagnosis in the hunt study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449868/
https://www.ncbi.nlm.nih.gov/pubmed/37438612
http://dx.doi.org/10.1038/s41416-023-02337-4
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