Circulating tumor cells in newly diagnosed inflammatory breast cancer
Genre
Journal ArticleDate
2015-01-15Author
Mego, MGiordano, A
De Giorgi, U
Masuda, H
Hsu, L
Giuliano, M
Fouad, TM
Dawood, S
Ueno, NT
Valero, V
Andreopoulou, E
Alvarez, RH
Woodward, WA
Hortobagyi, GN
Cristofanilli, M
Reuben, JM
Subject
AdultAged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
Female
Follow-Up Studies
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Inflammatory Breast Neoplasms
Kaplan-Meier Estimate
Middle Aged
Neoadjuvant Therapy
Neoplasm Staging
Neoplastic Cells, Circulating
Prognosis
Retrospective Studies
Risk Factors
Treatment Outcome
Young Adult
Permanent link to this record
http://hdl.handle.net/20.500.12613/5243
Metadata
Show full item recordDOI
10.1186/s13058-014-0507-6Abstract
© Mego et al. Introduction: Circulating 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. Methods: This 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 by using the CellSearch system before patients were started with chemotherapy. Results: The 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 fewer than five 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 five or more CTCs. Among patients with stage III IBC, there was a nonsignificant difference in PFS (HR=0.66; 95% confidence interval (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 with patients with one or more CTCs. In multivariate analysis, CTC was prognostic for PFS and OS independent of clinical stage. Conclusions: CTCs 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.Citation to related work
Springer Science and Business Media LLCHas part
Breast Cancer ResearchADA compliance
For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.eduae974a485f413a2113503eed53cd6c53
http://dx.doi.org/10.34944/dspace/5225