Clonality of circulating tumor cells in breast cancer brain metastasis patients

Bibliographic Details
Title: Clonality of circulating tumor cells in breast cancer brain metastasis patients
Authors: Carlotta Riebensahm, Simon A. Joosse, Malte Mohme, Annkathrin Hanssen, Jakob Matschke, Yvonne Goy, Isabell Witzel, Katrin Lamszus, Jolanthe Kropidlowski, Cordula Petersen, Anja Kolb-Kokocinski, Sascha Sauer, Kerstin Borgmann, Markus Glatzel, Volkmar Müller, Manfred Westphal, Sabine Riethdorf, Klaus Pantel, Harriet Wikman
Source: Breast Cancer Research, Vol 21, Iss 1, Pp 1-11 (2019)
Publisher Information: BMC, 2019.
Publication Year: 2019
Collection: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Subject Terms: CTC, Breast cancer, Brain metastases, Clonality, CNA, NGS, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
More Details: Abstract Background The incidence of brain metastases in breast cancer (BCBM) patients is increasing. These patients have a very poor prognosis, and therefore, identification of blood-based biomarkers, such as circulating tumor cells (CTCs), and understanding the genomic heterogeneity could help to personalize treatment options. Methods Both EpCAM-dependent (CellSearch® System) and EpCAM-independent Ficoll-based density centrifugation methods were used to detect CTCs from 57 BCBM patients. DNA from individual CTCs and corresponding primary tumors and brain metastases were analyzed by next-generation sequencing (NGS) in order to evaluate copy number aberrations and single nucleotide variations (SNVs). Results CTCs were detected after EpCAM-dependent enrichment in 47.7% of the patients (≥ 5 CTCs/7.5 ml blood in 20.5%). The CTC count was associated with ERBB2 status (p = 0.029) of the primary tumor as well as with the prevalence of bone metastases (p = 0.021). EpCAM-independent enrichment revealed CTCs in 32.6% of the patients, especially among triple-negative breast cancer (TNBC) patients (70.0%). A positive CTC status after enrichment of either method was significantly associated with decreased overall survival time (p
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1465-542X
Relation: http://link.springer.com/article/10.1186/s13058-019-1184-2; https://doaj.org/toc/1465-542X
DOI: 10.1186/s13058-019-1184-2
Access URL: https://doaj.org/article/9ce323027a994649b8033de0443befc4
Accession Number: edsdoj.9ce323027a994649b8033de0443befc4
Database: Directory of Open Access Journals
More Details
ISSN:1465542X
DOI:10.1186/s13058-019-1184-2
Published in:Breast Cancer Research
Language:English