Pooled Analysis of the Prognostic Relevance of Circulating Tumor Cells in Primary Breast Cancer

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Pooled Analysis of the Prognostic Relevance of Circulating Tumor Cells in Primary Breast Cancer. / Janni, Wolfgang; Rack, Brigitte; Terstappen, Leon Wmm; Pierga, Jean-Yves; Taran, Florin-Andrei; Fehm, Tanja; Hall, Carolyn; de Groot, Marco; Bidard, Francois-Clement; Friedl, Thomas W P; Fasching, Peter A; Brucker, Sara Y; Pantel, Klaus; Lucci, Anthony.

in: CLIN CANCER RES, Jahrgang 22, Nr. 10, 01.05.2016, S. 2583-93.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Janni, W, Rack, B, Terstappen, LW, Pierga, J-Y, Taran, F-A, Fehm, T, Hall, C, de Groot, M, Bidard, F-C, Friedl, TWP, Fasching, PA, Brucker, SY, Pantel, K & Lucci, A 2016, 'Pooled Analysis of the Prognostic Relevance of Circulating Tumor Cells in Primary Breast Cancer', CLIN CANCER RES, Jg. 22, Nr. 10, S. 2583-93. https://doi.org/10.1158/1078-0432.CCR-15-1603

APA

Janni, W., Rack, B., Terstappen, L. W., Pierga, J-Y., Taran, F-A., Fehm, T., Hall, C., de Groot, M., Bidard, F-C., Friedl, T. W. P., Fasching, P. A., Brucker, S. Y., Pantel, K., & Lucci, A. (2016). Pooled Analysis of the Prognostic Relevance of Circulating Tumor Cells in Primary Breast Cancer. CLIN CANCER RES, 22(10), 2583-93. https://doi.org/10.1158/1078-0432.CCR-15-1603

Vancouver

Bibtex

@article{b5028f75c8c94efe9672db1a3f9a974f,
title = "Pooled Analysis of the Prognostic Relevance of Circulating Tumor Cells in Primary Breast Cancer",
abstract = "PURPOSE: Although unequivocal evidence has shown the prognostic relevance of circulating tumor cells (CTCs) in the peripheral blood of patients with metastatic breast cancer, less evidence is available for the prognostic relevance of CTCs at the time of primary diagnosis.PATIENTS AND METHODS: We conducted a pooled analysis of individual data from 3,173 patients with non-metastatic (Stage I-III) breast cancer from 5 breast cancer institutions. The prevalence and numbers of CTCs were assessed at the time of primary diagnosis with the United States Food and Drug Administration-cleared CellSearch{\textregistered} System (Janssen Diagnostics, LLC). Patient outcomes were analyzed using meta-analytic procedures, univariate log-rank tests, and multivariate Cox proportional hazard regression analyses. The median follow-up duration was 62.8 months.RESULTS: One or more CTCs were detected in 20.2% of the patients. CTC-positive patients had larger tumors, increased lymph node involvement, and a higher histological tumor grade than did CTC-negative patients (all P < 0.002). Multivariate Cox regressions, which included tumor size, nodal status, histological tumor grade, and hormone-receptor and HER2 status, confirmed that the presence of CTCs was an independent prognostic factor for disease-free survival (hazard ratio (HR), 1.82; 95% confidence interval (CI), 1.47 to 2.26), distant disease-free survival (HR, 1.89; 95% CI, 1.49 to 2.40), breast cancer-specific survival (HR, 2.04; 95% CI, 1.52 to 2.75), and overall survival (HR, 1.97; 95% CI, 1.51 to 2.59).CONCLUSION: In patients with primary breast cancer, the presence of CTC was an independent predictor of poor disease-free, overall, breast-cancer-specific, and distant disease-free survival.",
author = "Wolfgang Janni and Brigitte Rack and Terstappen, {Leon Wmm} and Jean-Yves Pierga and Florin-Andrei Taran and Tanja Fehm and Carolyn Hall and {de Groot}, Marco and Francois-Clement Bidard and Friedl, {Thomas W P} and Fasching, {Peter A} and Brucker, {Sara Y} and Klaus Pantel and Anthony Lucci",
note = "Copyright {\textcopyright} 2015, American Association for Cancer Research.",
year = "2016",
month = may,
day = "1",
doi = "10.1158/1078-0432.CCR-15-1603",
language = "English",
volume = "22",
pages = "2583--93",
journal = "CLIN CANCER RES",
issn = "1078-0432",
publisher = "American Association for Cancer Research Inc.",
number = "10",

}

RIS

TY - JOUR

T1 - Pooled Analysis of the Prognostic Relevance of Circulating Tumor Cells in Primary Breast Cancer

AU - Janni, Wolfgang

AU - Rack, Brigitte

AU - Terstappen, Leon Wmm

AU - Pierga, Jean-Yves

AU - Taran, Florin-Andrei

AU - Fehm, Tanja

AU - Hall, Carolyn

AU - de Groot, Marco

AU - Bidard, Francois-Clement

AU - Friedl, Thomas W P

AU - Fasching, Peter A

AU - Brucker, Sara Y

AU - Pantel, Klaus

AU - Lucci, Anthony

N1 - Copyright © 2015, American Association for Cancer Research.

PY - 2016/5/1

Y1 - 2016/5/1

N2 - PURPOSE: Although unequivocal evidence has shown the prognostic relevance of circulating tumor cells (CTCs) in the peripheral blood of patients with metastatic breast cancer, less evidence is available for the prognostic relevance of CTCs at the time of primary diagnosis.PATIENTS AND METHODS: We conducted a pooled analysis of individual data from 3,173 patients with non-metastatic (Stage I-III) breast cancer from 5 breast cancer institutions. The prevalence and numbers of CTCs were assessed at the time of primary diagnosis with the United States Food and Drug Administration-cleared CellSearch® System (Janssen Diagnostics, LLC). Patient outcomes were analyzed using meta-analytic procedures, univariate log-rank tests, and multivariate Cox proportional hazard regression analyses. The median follow-up duration was 62.8 months.RESULTS: One or more CTCs were detected in 20.2% of the patients. CTC-positive patients had larger tumors, increased lymph node involvement, and a higher histological tumor grade than did CTC-negative patients (all P < 0.002). Multivariate Cox regressions, which included tumor size, nodal status, histological tumor grade, and hormone-receptor and HER2 status, confirmed that the presence of CTCs was an independent prognostic factor for disease-free survival (hazard ratio (HR), 1.82; 95% confidence interval (CI), 1.47 to 2.26), distant disease-free survival (HR, 1.89; 95% CI, 1.49 to 2.40), breast cancer-specific survival (HR, 2.04; 95% CI, 1.52 to 2.75), and overall survival (HR, 1.97; 95% CI, 1.51 to 2.59).CONCLUSION: In patients with primary breast cancer, the presence of CTC was an independent predictor of poor disease-free, overall, breast-cancer-specific, and distant disease-free survival.

AB - PURPOSE: Although unequivocal evidence has shown the prognostic relevance of circulating tumor cells (CTCs) in the peripheral blood of patients with metastatic breast cancer, less evidence is available for the prognostic relevance of CTCs at the time of primary diagnosis.PATIENTS AND METHODS: We conducted a pooled analysis of individual data from 3,173 patients with non-metastatic (Stage I-III) breast cancer from 5 breast cancer institutions. The prevalence and numbers of CTCs were assessed at the time of primary diagnosis with the United States Food and Drug Administration-cleared CellSearch® System (Janssen Diagnostics, LLC). Patient outcomes were analyzed using meta-analytic procedures, univariate log-rank tests, and multivariate Cox proportional hazard regression analyses. The median follow-up duration was 62.8 months.RESULTS: One or more CTCs were detected in 20.2% of the patients. CTC-positive patients had larger tumors, increased lymph node involvement, and a higher histological tumor grade than did CTC-negative patients (all P < 0.002). Multivariate Cox regressions, which included tumor size, nodal status, histological tumor grade, and hormone-receptor and HER2 status, confirmed that the presence of CTCs was an independent prognostic factor for disease-free survival (hazard ratio (HR), 1.82; 95% confidence interval (CI), 1.47 to 2.26), distant disease-free survival (HR, 1.89; 95% CI, 1.49 to 2.40), breast cancer-specific survival (HR, 2.04; 95% CI, 1.52 to 2.75), and overall survival (HR, 1.97; 95% CI, 1.51 to 2.59).CONCLUSION: In patients with primary breast cancer, the presence of CTC was an independent predictor of poor disease-free, overall, breast-cancer-specific, and distant disease-free survival.

U2 - 10.1158/1078-0432.CCR-15-1603

DO - 10.1158/1078-0432.CCR-15-1603

M3 - SCORING: Journal article

C2 - 26733614

VL - 22

SP - 2583

EP - 2593

JO - CLIN CANCER RES

JF - CLIN CANCER RES

SN - 1078-0432

IS - 10

ER -