Undetectable Tumor Cell-Free DNA in a Patient With Metastatic Breast Cancer With Complete Response and Long-Term Remission.
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Biomarkers, Tumor
Breast Neoplasms
/ diagnosis
Circulating Tumor DNA
DNA, Neoplasm
Female
Genetic Testing
Humans
Molecular Targeted Therapy
Neoplasm Metastasis
Neoplasm Staging
Precision Medicine
Receptor, ErbB-2
/ genetics
Receptors, Estrogen
/ genetics
Receptors, Progesterone
/ genetics
Remission Induction
Tomography, X-Ray Computed
Treatment Outcome
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
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
375-379Subventions
Organisme : NCI NIH HHS
ID : R01 CA214494
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA194024
Pays : United States