Circulating tumour cells in non-metastatic breast cancer: a prospective study

被引:410
作者
Lucci, Anthony [1 ]
Hall, Carolyn S.
Lodhi, Ashutosh K.
Bhattacharyya, Anirban
Anderson, Amber E.
Xiao, Lianchun [3 ]
Bedrosian, Isabelle
Kuerer, Henry M.
Krishnamurthy, Savitri [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Surg Oncol, Unit 444, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
关键词
BONE-MARROW; PERIPHERAL-BLOOD; FOLLOW-UP; CLINICAL-SIGNIFICANCE; ESTROGEN-RECEPTOR; STEM-CELL; PROGRESSION; DISSECTION; RECURRENCE; MASTECTOMY;
D O I
10.1016/S1470-2045(12)70209-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The identification of circulating tumour cells correlate with poor prognosis in metastatic breast cancer, but there are few data describing the importance of circulating tumour cells in patients with non-metastatic disease. Our aim was to establish if circulating tumour cells predicted worse outcome in patients with non-metastatic breast cancer. Methods We prospectively collected data on circulating tumour cells at the time of definitive surgery from chemonaive patients with stage 1-3 breast cancer from February, 2005, to December, 2010. We deemed eligible all patients with operable breast cancer presenting at The University of Texas MD Anderson Cancer Center (Houston, TX, USA). Patients were ineligible if they had bilateral breast cancer or any other malignancy within 5 years of the diagnosis of the present cancer. We measured circulating tumour cells with the CellSearch System (Veridex, Raritan, NJ). We correlated findings of circulating tumour cells with standard tumour characteristics, including tumour size and grade; oestrogen and progesterone receptor and human epidural growth factor receptor 2 (HER2) status; and axillary lymph node status with chi(2) or Fisher exact tests. We assessed outcomes at a median follow-up of 35 months. Log-rank test and Cox regression analysis was applied to establish the association of circulating tumour cells with progression-free and overall survival. Findings No patients reported adverse events or complications from blood collections. We identified one or more circulating tumour cells in 73 (24%) of 302 patients. Detection of one or more circulating tumour cells predicted both decreased progression-free survival (log-rank p=0.005; hazard ratio [HR] 4.62, 95% CI 1.79-11.9) and overall survival (log-rank p= 0.01; HR 4.04, 1.28-12.8). Interpretation The presence of one or more circulating tumour cells predicted early recurrence and decreased overall survival in chemonaive patients with non-metastatic breast cancer. These results suggest that assessment of circulating tumour cells might provide important prognostic information in these patients.
引用
收藏
页码:688 / 695
页数:8
相关论文
共 36 条
[1]   Stem cell and epithelial-mesenchymal transition markers are frequently overexpressed in circulating tumor cells of metastatic breast cancer patients [J].
Aktas, Bahriye ;
Tewes, Mitra ;
Fehm, Tanja ;
Hauch, Siegfried ;
Kimmig, Rainer ;
Kasimir-Bauer, Sabine .
BREAST CANCER RESEARCH, 2009, 11 (04)
[2]   Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases [J].
Allard, WJ ;
Matera, J ;
Miller, MC ;
Repollet, M ;
Connelly, MC ;
Rao, C ;
Tibbe, AGJ ;
Uhr, JW ;
Terstappen, LWMM .
CLINICAL CANCER RESEARCH, 2004, 10 (20) :6897-6904
[3]  
[Anonymous], J CLIN ONCOL S
[4]  
[Anonymous], CANC STAG MAN
[5]   Real- time RT-PCR detection of disseminated tumour cells in bone marrow has superior prognostic significance in comparison with circulating tumour cells in patients with breast cancer [J].
Benoy, IH ;
Elst, H ;
Philips, M ;
Wuyts, H ;
Van Dam, P ;
Scharpé, S ;
Van Marck, E ;
Vermeulen, PB ;
Dirix, LY .
BRITISH JOURNAL OF CANCER, 2006, 94 (05) :672-680
[6]   Single circulating tumor cell detection and overall survival in nonmetastatic breast cancer [J].
Bidard, F. -C. ;
Mathiot, C. ;
Delaloge, S. ;
Brain, E. ;
Giachetti, S. ;
de Cremoux, P. ;
Marty, M. ;
Pierga, J. -Y. .
ANNALS OF ONCOLOGY, 2010, 21 (04) :729-733
[7]  
BLACK MM, 1957, SURG GYNECOL OBSTET, V105, P97
[8]   Circulating tumor cells, disease progression, and survival in metastatic breast cancer [J].
Cristofanilli, M ;
Budd, GT ;
Ellis, MJ ;
Stopeck, A ;
Matera, J ;
Miller, MC ;
Reuben, JM ;
Doyle, GV ;
Allard, WJ ;
Terstappen, LWMM ;
Hayes, DF .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) :781-791
[9]   Detection of cytokeratin-19 mRNA-positive cells in the peripheral blood and bone marrow of patients with operable breast cancer [J].
Daskalaki, A. ;
Agelaki, S. ;
Perraki, M. ;
Apostolaki, S. ;
Xenidis, N. ;
Stathopoulos, E. ;
Kontopodis, E. ;
Hatzidaki, D. ;
Mavroudis, D. ;
Georgoulias, V. .
BRITISH JOURNAL OF CANCER, 2009, 101 (04) :589-597
[10]   Time distribution of the recurrence risk for breast cancer patients undergoing mastectomy: Further support about the concept of tumor dormancy [J].
Demicheli, R ;
Abbattista, A ;
Miceli, R ;
Valagussa, P ;
Bonadonna, G .
BREAST CANCER RESEARCH AND TREATMENT, 1996, 41 (02) :177-185