Liquid biopsies come of age: towards implementation of circulating tumour DNA
Accepted version
Peer-reviewed
Repository URI
Repository DOI
Change log
Authors
Wan, JCM
Massie, Charles https://orcid.org/0000-0003-2314-4843
Garcia-Corbacho, J
Mouliere, Florent https://orcid.org/0000-0001-7043-0514
Brenton, James https://orcid.org/0000-0002-5738-6683
Abstract
Improvements in genomic and molecular methods are expanding the range of potential applications for circulating tumour DNA (ctDNA), both in a research setting and as a ‘liquid biopsy’ for cancer management. Proof-of-principle studies have demonstrated the translational potential of ctDNA for prognostication, molecular profiling and monitoring. The field is now in an exciting transitional period in which ctDNA analysis is beginning to be applied clinically, although there is still much to learn about the biology of cell-free DNA. This is an opportune time to appraise potential approaches to ctDNA analysis, and to consider their applications in personalized oncology and in cancer research.
Description
Keywords
cancer genomics, cancer screening, cancer therapeutic resistance, DNA, personalized medicine
Journal Title
Nature Reviews Cancer
Conference Name
Journal ISSN
1474-175X
1474-1768
1474-1768
Volume Title
17
Publisher
Nature Publishing Group
Publisher DOI
Sponsorship
European Research Council (337905)
Cancer Research UK (C14303/A17197)
Cancer Research UK (15601)
Cancer Research UK (16942)
Cancer Research UK (22905)
Cancer Research UK (20240)
Cancer Research UK (C14303/A17197)
Cancer Research UK (15601)
Cancer Research UK (16942)
Cancer Research UK (22905)
Cancer Research UK (20240)
We would like to acknowledge the support of The University of Cambridge, Cancer Research UK (grant numbers A11906, A20240, A15601) (to N.R., J.D.B.), the European Research Council under the European Union's Seventh Framework Programme (FP/2007-2013)/ERC Grant Agreement n. 337905 (to N.R.), the Cambridge Experimental Cancer Medicine Centre, and Hutchison Whampoa Limited (to N.R.), AstraZeneca (to R.B., S.P.), the Cambridge Experimental Cancer Medicine Centre (ECMC) (to R.B., S.P.), and NIHR Biomedical Research Centre (BRC) (to R.B., S.P.). J.G.C. acknowledges clinical fellowship support from SEOM.