Your browser doesn't support javascript.
loading
Circulating tumor cells in newly diagnosed inflammatory breast cancer.
Mego, Michal; Giordano, Antonio; De Giorgi, Ugo; Masuda, Hiroko; Hsu, Limin; Giuliano, Mario; Fouad, Tamer M; Dawood, Shaheenah; Ueno, Naoto T; Valero, Vicente; Andreopoulou, Eleni; Alvarez, Ricardo H; Woodward, Wendy A; Hortobagyi, Gabriel N; Cristofanilli, Massimo; Reuben, James M.
Afiliação
  • Mego M; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA. misomego@gmail.com.
  • Giordano A; Department of Medical Oncology, Comenius University, School of Medicine, Bratislava, Slovakia. misomego@gmail.com.
  • De Giorgi U; Present affiliation: Breast Center, Thomas Jefferson University-Kimmel Cancer Center, Philadelphia, PA, USA. misomego@gmail.com.
  • Masuda H; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA. agiordanomd@gmail.com.
  • Hsu L; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA. u_degiorgi@yahoo.com.
  • Giuliano M; Medical Oncology, Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) - IRCCS, Meldola, FC, Italy. u_degiorgi@yahoo.com.
  • Fouad TM; Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. hmasuda@onh.go.jp.
  • Dawood S; Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. lhsu@mdanderson.org.
  • Ueno NT; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA. giuliano@bcm.edu.
  • Valero V; Department of Clinical Medicine and Surgery, University Federico II, Naples, Italy. giuliano@bcm.edu.
  • Andreopoulou E; Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. TFouad@mdanderson.org.
  • Alvarez RH; Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. sdawood@yahoo.com.
  • Woodward WA; Medical Oncology Department, Dubai Hospital, Dubai, UAE. sdawood@yahoo.com.
  • Hortobagyi GN; Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. nueno@mdanderson.org.
  • Cristofanilli M; Morgan Welch Inflammatory Breast Cancer Research Program and Clinic, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. nueno@mdanderson.org.
  • Reuben JM; Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. vvalero@mdanderson.org.
Breast Cancer Res ; 17: 2, 2015 Jan 09.
Article em En | MEDLINE | ID: mdl-25572591
ABSTRACT

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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Inflamatórias Mamárias / Células Neoplásicas Circulantes Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Inflamatórias Mamárias / Células Neoplásicas Circulantes Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Middle aged Idioma: En Revista: Breast Cancer Res Assunto da revista: NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Estados Unidos