Circulating Tumor DNA: A Step into the Future of Cancer Management.


Journal

Acta cytologica
ISSN: 1938-2650
Titre abrégé: Acta Cytol
Pays: Switzerland
ID NLM: 0370307

Informations de publication

Date de publication:
2019
Historique:
received: 13 07 2018
accepted: 13 08 2018
pubmed: 11 3 2019
medline: 17 10 2019
entrez: 11 3 2019
Statut: ppublish

Résumé

Liquid biopsy was introduced to the oncology field with the promise of revolutionizing the management of cancer patients, minimizing the exposure to invasive procedures such as tissue biopsy, and providing reliable information regarding therapy response and detection of disease relapse. Despite the significant increase in the number of published studies on circulating tumor DNA (ctDNA) in the past years, the emphasis of most studies is on the development of new technologies or on the clinical utility of ctDNA. This leaves a clear gap of knowledge concerning the biology of ctDNA, such as the fundamental mechanisms through which DNA from tumor cells is released into the circulation. Moreover, considering that ctDNA analysis is now currently being applied in clinical practice, the need for rigorous quality control is arising, and with it the necessity to standardize procedures, from sample collection to data analysis. This review focuses on the main aspects of ctDNA, including approaches currently available to evaluate tumor genetics, as well as the points that still require improvement in order to make liquid biopsy a key player in precision medicine.

Identifiants

pubmed: 30852572
pii: 000492917
doi: 10.1159/000492917
doi:

Substances chimiques

Antineoplastic Agents 0
Biomarkers, Tumor 0
Circulating Tumor DNA 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

456-465

Informations de copyright

© 2019 S. Karger AG, Basel.

Auteurs

Joana Fernandes Marques (J)

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.

Joana Pereira Reis (J)

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
Faculty of Medicine, University of Porto, Porto, Portugal.

Gabriela Fernandes (G)

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
Department of Pulmonology, Hospital de São João, Porto, Portugal.

Venceslau Hespanhol (V)

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
Department of Pulmonology, Hospital de São João, Porto, Portugal.

José Carlos Machado (JC)

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
Faculty of Medicine, University of Porto, Porto, Portugal.

José Luís Costa (JL)

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal, jcosta@ipatimup.pt.
IPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal, jcosta@ipatimup.pt.
Faculty of Medicine, University of Porto, Porto, Portugal, jcosta@ipatimup.pt.

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