Title |
Circulating tumor cells in newly diagnosed inflammatory breast cancer
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Published in |
Breast Cancer Research, January 2015
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DOI | 10.1186/s13058-014-0507-6 |
Pubmed ID | |
Authors |
Michal Mego, Antonio Giordano, Ugo De Giorgi, Hiroko Masuda, Limin Hsu, Mario Giuliano, Tamer M Fouad, Shaheenah Dawood, Naoto T Ueno, Vicente Valero, Eleni Andreopoulou, Ricardo H Alvarez, Wendy A Woodward, Gabriel N Hortobagyi, Massimo Cristofanilli, James M Reuben |
Abstract |
IntroductionCirculating tumor cells (CTCs) are an independent prognostic factor for progression-free survival (PFS) and overall survival (OS) in patients with metastatic breast cancer. Inflammatory breast cancer (IBC) is one of the most aggressive forms of breast cancer. The prognostic value of a CTC count in newly diagnosed IBC has not been established. The aim of this study was to assess the prognostic value of a baseline CTC count in patients with newly diagnosed IBC.MethodsThis retrospective study included 147 patients with newly diagnosed IBC (77 with locally advanced and 70 with metastatic IBC) treated with neoadjuvant therapy or first-line chemotherapy during the period from January 2004 through December 2012 at The University of Texas MD Anderson Cancer Center. CTCs were detected and enumerated using the CellSearch system before patients were started with chemotherapy.ResultsThe proportion of patients with ¿1 CTC was lower among patients with stage III than among patients with metastatic IBC (54.5% versus 84.3%; P¿=¿0.0002); the proportion of patients with ¿5 CTCs was also lower for stage III than for metastatic IBC (19.5% versus 47.1%; P¿=¿0.0004). Patients with <5 CTCs had significantly better progression-free survival (PFS) (hazard ratio [HR]¿=¿0.60; P¿=¿0.02) and overall survival (HR¿=¿0.59; P¿=¿0.03) than patients with ¿5 CTCs. Among patients with stage III IBC, there was non-significant difference in PFS (HR¿=¿0.66; 95% confidence ratio (CI), 0.31 to 1.39; P¿=¿0.29) and OS (HR¿=¿0.54; 95% CI, 0.24 to 1.26; P¿=¿0.48) in patients with no CTCs compared to patients with ¿1 CTCs. In multivariate analysis, CTC was prognostic for PFS and OS independently from clinical stage.ConclusionsCTCs can be detected in a large proportion of patients with newly diagnosed IBC and are a strong predictor of worse prognosis in patients with newly diagnosed IBC. |
X Demographics
Geographical breakdown
Country | Count | As % |
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United States | 11 | 69% |
Netherlands | 1 | 6% |
Unknown | 4 | 25% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 11 | 69% |
Practitioners (doctors, other healthcare professionals) | 4 | 25% |
Scientists | 1 | 6% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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United States | 1 | 2% |
Brazil | 1 | 2% |
Unknown | 54 | 96% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Ph. D. Student | 9 | 16% |
Researcher | 8 | 14% |
Student > Bachelor | 7 | 13% |
Student > Postgraduate | 5 | 9% |
Student > Master | 5 | 9% |
Other | 10 | 18% |
Unknown | 12 | 21% |
Readers by discipline | Count | As % |
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Medicine and Dentistry | 22 | 39% |
Agricultural and Biological Sciences | 8 | 14% |
Nursing and Health Professions | 3 | 5% |
Biochemistry, Genetics and Molecular Biology | 2 | 4% |
Chemistry | 2 | 4% |
Other | 5 | 9% |
Unknown | 14 | 25% |