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Circulating DNA and frequency of colorectal cancer brain metastases in a presumed high-risk group

This explorative prospective observational pilot study investigated if suggested risk factors, rectal cancer and lung metastases, could add to a relevant detection rate of asymptomatic brain metastases (BM) from colorectal cancer (CRC). Secondary, prognostic biological aspects were investigated by t...

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Autores principales: Callesen, Louise Bach, Boysen, Anders Kindberg, Andersen, Rikke Fredslund, Dalby, Rikke Beese, Spindler, Karen-Lise Garm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616067/
https://www.ncbi.nlm.nih.gov/pubmed/37903871
http://dx.doi.org/10.1038/s41598-023-45939-x
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author Callesen, Louise Bach
Boysen, Anders Kindberg
Andersen, Rikke Fredslund
Dalby, Rikke Beese
Spindler, Karen-Lise Garm
author_facet Callesen, Louise Bach
Boysen, Anders Kindberg
Andersen, Rikke Fredslund
Dalby, Rikke Beese
Spindler, Karen-Lise Garm
author_sort Callesen, Louise Bach
collection PubMed
description This explorative prospective observational pilot study investigated if suggested risk factors, rectal cancer and lung metastases, could add to a relevant detection rate of asymptomatic brain metastases (BM) from colorectal cancer (CRC). Secondary, prognostic biological aspects were investigated by translational analysis of plasma samples. The study enrolled patients with rectal cancer and lung metastases. At inclusion, patients underwent a standard MRI scan of the brain. Cell-free DNA (cfDNA) level was measured by a direct fluorescence assay (DFA), and circulating tumor DNA (ctDNA) by ddPCR. BM was detected in one of twenty-nine included patients. Patients had higher cfDNA levels than healthy subjects (p < 0.01). Patients with the primary tumor in situ had higher cfDNA levels than those with resected primary tumor (p < 0.01). Patients with liver involvement had higher cfDNA levels (p = 0.12) and circulating tumor DNA levels (p = 0.01) than those without liver involvement. In conclusion, the modest incidence of BM does not justify routine MRI of the brain in this selected population. cfDNA by DFA could be a valuable tool when planning treatment and follow-up for CRC patients. Future studies should focus on identifying further characteristics and biomarkers associated with a high risk of BM, enhancing the possibility for early intervention.
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spelling pubmed-106160672023-11-01 Circulating DNA and frequency of colorectal cancer brain metastases in a presumed high-risk group Callesen, Louise Bach Boysen, Anders Kindberg Andersen, Rikke Fredslund Dalby, Rikke Beese Spindler, Karen-Lise Garm Sci Rep Article This explorative prospective observational pilot study investigated if suggested risk factors, rectal cancer and lung metastases, could add to a relevant detection rate of asymptomatic brain metastases (BM) from colorectal cancer (CRC). Secondary, prognostic biological aspects were investigated by translational analysis of plasma samples. The study enrolled patients with rectal cancer and lung metastases. At inclusion, patients underwent a standard MRI scan of the brain. Cell-free DNA (cfDNA) level was measured by a direct fluorescence assay (DFA), and circulating tumor DNA (ctDNA) by ddPCR. BM was detected in one of twenty-nine included patients. Patients had higher cfDNA levels than healthy subjects (p < 0.01). Patients with the primary tumor in situ had higher cfDNA levels than those with resected primary tumor (p < 0.01). Patients with liver involvement had higher cfDNA levels (p = 0.12) and circulating tumor DNA levels (p = 0.01) than those without liver involvement. In conclusion, the modest incidence of BM does not justify routine MRI of the brain in this selected population. cfDNA by DFA could be a valuable tool when planning treatment and follow-up for CRC patients. Future studies should focus on identifying further characteristics and biomarkers associated with a high risk of BM, enhancing the possibility for early intervention. Nature Publishing Group UK 2023-10-30 /pmc/articles/PMC10616067/ /pubmed/37903871 http://dx.doi.org/10.1038/s41598-023-45939-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Callesen, Louise Bach
Boysen, Anders Kindberg
Andersen, Rikke Fredslund
Dalby, Rikke Beese
Spindler, Karen-Lise Garm
Circulating DNA and frequency of colorectal cancer brain metastases in a presumed high-risk group
title Circulating DNA and frequency of colorectal cancer brain metastases in a presumed high-risk group
title_full Circulating DNA and frequency of colorectal cancer brain metastases in a presumed high-risk group
title_fullStr Circulating DNA and frequency of colorectal cancer brain metastases in a presumed high-risk group
title_full_unstemmed Circulating DNA and frequency of colorectal cancer brain metastases in a presumed high-risk group
title_short Circulating DNA and frequency of colorectal cancer brain metastases in a presumed high-risk group
title_sort circulating dna and frequency of colorectal cancer brain metastases in a presumed high-risk group
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616067/
https://www.ncbi.nlm.nih.gov/pubmed/37903871
http://dx.doi.org/10.1038/s41598-023-45939-x
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