Circulating Tumor DNA in Breast Cancer: Current and Future Applications.

Circulating tumor DNA Liquid biopsy Minimal residual disease Molecular residual disease Precision oncology

Journal

Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731

Informations de publication

Date de publication:
10 2023
Historique:
received: 11 04 2023
revised: 14 06 2023
accepted: 17 06 2023
medline: 2 10 2023
pubmed: 13 7 2023
entrez: 12 7 2023
Statut: ppublish

Résumé

The assessment of plasma for circulating tumor DNA (ctDNA) via liquid biopsy has revolutionized our understanding of breast cancer pathogenesis and evolution. Historically, genotyping evaluation of breast cancer required invasive tissue biopsy, limiting potential for serial evaluation over the treatment course of advanced breast cancer, and not allowing for assessment for residual disease in early breast cancer after resection. However, technological advances over the years have led to an increase in the clinical use of ctDNA as a liquid biopsy for genotype-matched therapy selection and monitoring for patients undergoing treatment for advanced breast cancer. Furthermore, increasingly sensitive assays are being developed to facilitate detection of molecular evidence of residual or recurrent disease in localized breast cancer after definitive therapy. In this review, we discuss the current and future applications of ctDNA in breast cancer. Rational applications of ctDNA offer the potential to further refine patient-centered care and personalize treatment based on molecularly defined risk assessments for patients with breast cancer.

Identifiants

pubmed: 37438196
pii: S1526-8209(23)00165-9
doi: 10.1016/j.clbc.2023.06.008
pii:
doi:

Substances chimiques

Circulating Tumor DNA 0
Biomarkers, Tumor 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

687-692

Subventions

Organisme : NCI NIH HHS
ID : K08 CA252639
Pays : United States

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Disclosure Dr. Medford has consulted for Guardant Health, Illumina and Natera. Dr. Parsons has advised for Caris, Illumina, and SAGA. Institutional research funding has been provided by Puma Biotechnology. Dr. Bardia has consulted for Pfizer, Novartis, Genentech, Merck, Radius Health, Immunomedics/Gilead, Sanofi, Daiichi Pharma/Astra Zeneca, Phillips, Eli Lilly, and Foundation Medicine. Contracted research/grant to the institution has been provided by Genentech, Novartis, Pfizer, Merck, Sanofi, Radius Health, Immunomedics/Gilead, Daiichi Pharma/Astra Zeneca, and Eli Lilly.

Auteurs

Arielle J Medford (AJ)

Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA; Broad Institute of MIT & Harvard, Cambridge, MA. Electronic address: amedford@mgh.harvard.edu.

Elyssa N Denault (EN)

Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA.

Beverly Moy (B)

Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA.

Heather A Parsons (HA)

Dana Farber Cancer Institute, Boston MA.

Aditya Bardia (A)

Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA.

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Classifications MeSH