Cargando…
The impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients
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 sampli...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435916/ https://www.ncbi.nlm.nih.gov/pubmed/25972110 http://dx.doi.org/10.1186/s12885-015-1423-6 |
_version_ | 1782371977655222272 |
---|---|
author | 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 |
author_facet | 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 |
author_sort | Wallwiener, Markus |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4435916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44359162015-05-19 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 BMC Cancer Research Article 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. BioMed Central 2015-05-14 /pmc/articles/PMC4435916/ /pubmed/25972110 http://dx.doi.org/10.1186/s12885-015-1423-6 Text en © Wallwiener et al.; licensee BioMed Central. 2015 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article 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 The impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients |
title | The impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients |
title_full | The impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients |
title_fullStr | The impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients |
title_full_unstemmed | The impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients |
title_short | The impact of HER2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients |
title_sort | impact of her2 phenotype of circulating tumor cells in metastatic breast cancer: a retrospective study in 107 patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4435916/ https://www.ncbi.nlm.nih.gov/pubmed/25972110 http://dx.doi.org/10.1186/s12885-015-1423-6 |
work_keys_str_mv | AT wallwienermarkus theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT hartkopfandreasdaniel theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT riethdorfsabine theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT neesjuliane theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT sprickmartinronald theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT schonfischbirgitt theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT taranflorinandrei theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT heiljorg theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT sohnchristof theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT pantelklaus theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT trumppandreas theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT schneeweissandreas theimpactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT wallwienermarkus impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT hartkopfandreasdaniel impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT riethdorfsabine impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT neesjuliane impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT sprickmartinronald impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT schonfischbirgitt impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT taranflorinandrei impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT heiljorg impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT sohnchristof impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT pantelklaus impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT trumppandreas impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients AT schneeweissandreas impactofher2phenotypeofcirculatingtumorcellsinmetastaticbreastcanceraretrospectivestudyin107patients |