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The impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients

Wallwiener, Markus ; Hartkopf, Andreas Daniel ; Riethdorf, Sabine ; Nees, Juliane ; Sprick, Martin Ronald ; Schönfisch, Birgitt ; Taran, Florin-Andrei ; Heil, Jörg ; Sohn, Christof ; Pantel, Klaus ; Trumpp, Andreas ; Schneeweiss, Andreas

In: BMC cancer, 15 (2015), Nr. 403. pp. 1-7. ISSN 1471-2407

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Download (612kB) | Lizenz: Creative Commons LizenzvertragThe impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients by Wallwiener, Markus ; Hartkopf, Andreas Daniel ; Riethdorf, Sabine ; Nees, Juliane ; Sprick, Martin Ronald ; Schönfisch, Birgitt ; Taran, Florin-Andrei ; Heil, Jörg ; Sohn, Christof ; Pantel, Klaus ; Trumpp, Andreas ; Schneeweiss, Andreas underlies the terms of Creative Commons Attribution 3.0 Germany

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Abstract

Background: In metastatic breast cancer (MBC), antigen profiles of metastatic tissue and primary tumor differ in up to 20 % of patients. Reassessment of predictive markers, including human epidermal growth factor receptor 2 (HER2) expression, might help to optimize MBC treatment. While tissue sampling is invasive and often difficult to repeat, circulating tumor cell (CTC) analysis requires only a blood sample and might provide an easy-to-repeat, real-time “liquid biopsy” approach. The present retrospective study was conducted to compare HER2 expression in primary tumors, metastatic tissue, and circulating tumor cells (CTCs) from MBC patients and to analyze the potential impact of HER2 overexpression by CTCs on progression-free (PFS) and overall survival (OS) in MBC. Methods: CTC-positive (five or more CTCs/7.5 mL blood; CellSearch®, Janssen Diagnostics) MBC patients starting a new line of systemic treatment were eligible for the study. HER2 status of CTCs was determined by immunofluorescence (CellSearch®). HER2 status of primary (PRIM) and metastatic (MET) tumor tissue was determined by immunohistochemistry. Data were analyzed using descriptive statistics and Kaplan–Meier plots. Results: One hundred seven patients (median age (range) 57 (33–81) years) were included. 100/107 (93 %) patients were followed-up for a median [95 % confidence interval (CI)] of 28.5 [25.1–40.1] months. Of 37/107 (35 %) CTC-HER2-positive patients only 10 (27 %) were PRIM-HER2-positive. 6/46 (13 %) patients were MET-HER2-positive; only 2/10 (20 %) CTC-HER2-positive patients were MET-HER2-positive. Overall accuracy between CTC-HER2 expression and PRIM-HER2 and MET-HER2 status was 69 % and 74 %, respectively. Kaplan–Meier plots of PFS and OS by CTC-HER2 status revealed significantly longer median [95 % CI] PFS of CTC-HER2-positive versus CTC-HER2-negative patients (7.4 [4.7–13.7] versus 4.34 [3.5–5.9] months; p = 0.035). CTC-HER2-positive status showed no significant difference for OS (13.7 [7.7–30.0] versus 8.7 [5.9–15.3] months; p = 0.287). Conclusions: HER2 status can change during the course of breast cancer. CTC phenotyping may serve as an easy-to-perform “liquid biopsy” to reevaluate HER2 status and potentially guide treatment decisions. Further, prospective studies are needed.

Item Type: Article
Journal or Publication Title: BMC cancer
Volume: 15
Number: 403
Publisher: BioMed Central
Place of Publication: London
Date Deposited: 25 Nov 2015 09:32
Date: 2015
ISSN: 1471-2407
Page Range: pp. 1-7
Faculties / Institutes: Service facilities > German Cancer Research Center (DKFZ)
Medizinische Fakultät Heidelberg > Universitäts-Frauenklinik
Subjects: 610 Medical sciences Medicine
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