How liquid biopsies can change clinical practice in oncology.


Journal

Annals of oncology : official journal of the European Society for Medical Oncology
ISSN: 1569-8041
Titre abrégé: Ann Oncol
Pays: England
ID NLM: 9007735

Informations de publication

Date de publication:
01 10 2019
Historique:
pubmed: 3 8 2019
medline: 1 8 2020
entrez: 3 8 2019
Statut: ppublish

Résumé

Cell-free DNA fragments are shed into the bloodstream by tumor cells. The analysis of circulating tumor DNA (ctDNA), commonly known as liquid biopsy, can be exploited for a variety of clinical applications. ctDNA is being used to genotype solid cancers non-invasively, to track tumor dynamics and to detect the emergence of drug resistance. In a few settings, liquid biopsies have already entered clinical practice. For example, ctDNA is used to guide treatment in a subset of lung cancers. In this review, we discuss how recent improvements in the sensitivity and accuracy of ctDNA analyses have led to unprecedented advances in this research field. We further consider what is required for the routine deployment of liquid biopsies in the clinical diagnostic space. We pinpoint technical hurdles that liquid biopsies have yet to overcome, including preanalytical and analytical challenges. We foresee how liquid biopsies will transform clinical practice: by complementing (or replacing) imaging to monitor treatment response and by detecting minimal residual disease after surgery with curative intent.

Identifiants

pubmed: 31373349
pii: S0923-7534(19)60972-5
doi: 10.1093/annonc/mdz227
pii:
doi:

Substances chimiques

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

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1580-1590

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

G Siravegna (G)

Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy; Department of Oncology, University of Torino, Candiolo, Turin, Italy.

B Mussolin (B)

Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.

T Venesio (T)

Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.

S Marsoni (S)

IFOM, Istituto FIRC di Oncología Molecolare, Milan, Italy.

J Seoane (J)

Vall d'Hebron Institute of Oncology, Vall d'Hebron University Hospital and Universitat Autonoma de Barcelona, CIBERONC, Barcelona, Spain; Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain.

C Dive (C)

Clinical and Experimental Pharmacology Group and Manchester Centre for Cancer Biomarker Sciences, Cancer Research UK Manchester Institute, University of Manchester, Manchester, UK.

N Papadopoulos (N)

Ludwig Center for Cancer Genetics and Therapeutics, Johns Hopkins University School of Medicine, Baltimore, USA; Sidney Kimmel Cancer Center, Johns Hopkins University School of Medicine, Baltimore, USA.

S Kopetz (S)

Division of Cancer Medicine, Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA.

R B Corcoran (RB)

Massachusetts General Hospital Cancer Center and Department of Medicine, Harvard Medical School, Boston, USA.

L L Siu (LL)

Princess Margaret Cancer Centre, University of Toronto, Toronto, Canada.

A Bardelli (A)

Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy; Department of Oncology, University of Torino, Candiolo, Turin, Italy. Electronic address: alberto.bardelli@unito.it.

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Classifications MeSH