Undetectable Tumor Cell-Free DNA in a Patient With Metastatic Breast Cancer With Complete Response and Long-Term Remission.


Journal

Journal of the National Comprehensive Cancer Network : JNCCN
ISSN: 1540-1413
Titre abrégé: J Natl Compr Canc Netw
Pays: United States
ID NLM: 101162515

Informations de publication

Date de publication:
04 2020
Historique:
received: 02 08 2019
accepted: 25 11 2019
entrez: 8 4 2020
pubmed: 8 4 2020
medline: 17 6 2021
Statut: ppublish

Résumé

The ability to serially monitor tumor-derived cell-free DNA (cfDNA) brings with it the potential to measure response to anticancer therapies and detect minimal residual disease (MRD). This report describes a patient with HER2-positive metastatic breast cancer with an exceptional response to trastuzumab and nab-paclitaxel who remains in complete remission several years after cessation of therapy. Next-generation sequencing of the patient's primary tumor tissue showed several mutations, including an oncogenic hotspot PIK3CA mutation. A sample of cfDNA was collected 6 years after her last therapy and then analyzed for mutant PIK3CA using digital PCR. No detectable mutations associated with the primary tumor were found despite assaying >10,000 genome equivalents, suggesting that the patient had achieved a molecular remission. Results of this case study suggest that serial monitoring of MRD using liquid biopsies could provide a useful method for individualizing treatment plans for patients with metastatic disease with extreme responses to therapy. However, large-scale clinical studies are needed to validate and implement these techniques for patient care.

Identifiants

pubmed: 32259780
doi: 10.6004/jnccn.2019.7381
pii: jnccn19208
doi:
pii:

Substances chimiques

Biomarkers, Tumor 0
Circulating Tumor DNA 0
DNA, Neoplasm 0
Receptors, Estrogen 0
Receptors, Progesterone 0
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Case Reports Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

375-379

Subventions

Organisme : NCI NIH HHS
ID : R01 CA214494
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA194024
Pays : United States

Auteurs

Natasha Hunter (N)

Fred Hutchinson/University of Washington Cancer Consortium, Seattle, Washington.

Sarah Croessmann (S)

Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee; and.

Karen Cravero (K)

The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, Maryland.

Daniel Shinn (D)

The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, Maryland.

Paula J Hurley (PJ)

Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee; and.
The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, Maryland.

Ben Ho Park (BH)

Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee; and.
The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, Maryland.

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Classifications MeSH