Clinical application of circulating tumour DNA in colorectal cancer.


Journal

The lancet. Gastroenterology & hepatology
ISSN: 2468-1253
Titre abrégé: Lancet Gastroenterol Hepatol
Pays: Netherlands
ID NLM: 101690683

Informations de publication

Date de publication:
09 2023
Historique:
received: 23 03 2023
revised: 07 05 2023
accepted: 09 05 2023
medline: 14 8 2023
pubmed: 28 7 2023
entrez: 27 7 2023
Statut: ppublish

Résumé

Liquid biopsies that detect circulating tumour DNA (ctDNA) have the potential to revolutionise the personalised management of colorectal cancer. For patients with early-stage disease, emerging clinical applications include the assessment of molecular residual disease after surgery, the monitoring of adjuvant chemotherapy efficacy, and early detection of recurrence during surveillance. In the advanced disease setting, data highlight the potential of ctDNA levels as a prognostic marker and as an early indicator of treatment response. ctDNA assessment can complement standard tissue-based testing for molecular characterisation, with the added ability to monitor emerging mutations under the selective pressure of targeted therapy. Here we provide an overview of the evidence supporting the use of ctDNA in colorectal cancer, the studies underway to address some of the outstanding questions, and the barriers to widespread clinical uptake.

Identifiants

pubmed: 37499673
pii: S2468-1253(23)00146-2
doi: 10.1016/S2468-1253(23)00146-2
pii:
doi:

Substances chimiques

Circulating Tumor DNA 0
Biomarkers, Tumor 0
DNA, Neoplasm 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

837-852

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Interests PG has received consulting fees from Haystack Oncology and honoraria from Amgen, Roche, Servier, Merck, Pierre-Fabre, and MSD. JT has received consulting fees from Haystack Oncology and Seres Therapeutics, honoraria from Astra Zeneca, Amgen, and Servier, support for attending meetings from Roche, participated on advisory boards for Beigene, Novartis, Astra Zeneca, Merck, Serono, MSD, Pierre Fabre, BMS, Daichii Sankyo, Takeda, Illumina, and Gilead, and has a leadership role on AGITG and ESMO. All other authors declare no competing interests.

Auteurs

Matthew Loft (M)

Division of Personalised Oncology, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville, VIC, Australia; Department of Medical Oncology, Western Health, Footscray, VIC, Australia.

Yat Hang To (YH)

Division of Personalised Oncology, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville, VIC, Australia; Department of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC, Australia.

Peter Gibbs (P)

Division of Personalised Oncology, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville, VIC, Australia; Department of Medical Oncology, Western Health, Footscray, VIC, Australia.

Jeanne Tie (J)

Division of Personalised Oncology, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia; Department of Medical Biology, University of Melbourne, Parkville, VIC, Australia; Department of Medical Oncology, Peter MacCallum Cancer Centre, Parkville, VIC, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VIC, Australia. Electronic address: jeanne.tie@petermac.org.

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Classifications MeSH