Circulating Tumor Cells: A Useful Predictor of Treatment Efficacy in Metastatic Breast Cancer

被引:270
作者
Liu, Minetta C. [1 ]
Shields, Peter G.
Warren, Robert D.
Cohen, Philip
Wilkinson, Mary
Ottaviano, Yvonne L.
Rao, Suman B.
Eng-Wong, Jennifer
Seillier-Moiseiwitsch, Francoise
Noone, Anne-Michelle
Isaacs, Claudine
机构
[1] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA
关键词
PERIPHERAL-BLOOD; DISEASE PROGRESSION; FOLLOW-UP; CARCINOCYTHEMIA; CARCINOMA; SURVIVAL; LEUKEMIA; MICROMETASTASES; STATISTICS; POOR;
D O I
10.1200/JCO.2008.20.6664
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose Five or more circulating tumor cells (CTCs) per 7.5 mL of blood predicts for poorer progression-free survival (PFS) in patients with metastatic breast cancer (MBC). We conducted a prospective study to demonstrate that CTC results correlate strongly with radiographic disease progression at the time of and in advance of imaging. Patients and Methods Serial CTC levels were obtained in patients starting a new treatment regimen for progressive, radiographically measurable MBC. Peripheral blood was collected for CTC enumeration at baseline and at 3- to 4-week intervals. Clinical outcomes were based on radiographic studies performed in 9- to 12-week intervals. Results Sixty-eight patients were evaluable for the CTC-imaging correlations, and 74 patients were evaluable for the PFS analysis. Median follow-up was 13.3 months. A statistically significant correlation was demonstrated between CTC levels and radiographic disease progression in patients receiving chemotherapy or endocrine therapy. This correlation applied to CTC results obtained at the time of imaging (odds ratio [OR], 6.3), 3 to 5 weeks before imaging (OR, 3.1), and 7 to 9 weeks before imaging (OR, 4.9). Results from analyses stratified by type of therapy remained statistically significant. Shorter PFS was observed for patients with five or more CTCs at 3 to 5 weeks and at 7 to 9 weeks after the start of treatment. Conclusion We provide, to our knowledge, the first evidence of a strong correlation between CTC results and radiographic disease progression in patients receiving chemotherapy or endocrine therapy for MBC. These findings support the role of CTC enumeration as an adjunct to standard methods of monitoring disease status in MBC.
引用
收藏
页码:5153 / 5159
页数:7
相关论文
共 38 条
[1]
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
[2]
[Anonymous], 1869, The Australian Medical Journal
[3]
Bauernhofer T, 2005, ONCOL REP, V13, P179
[4]
Beveridge R., 2007, COMMUN ONCOL, V4, P79
[5]
Molecular characterization of minimal residual cancer cells in patients with solid tumors [J].
Böckmann, B ;
Grill, HJ ;
Giesing, M .
BIOMOLECULAR ENGINEERING, 2001, 17 (03) :95-111
[6]
Circulating tumor cells versus imaging - Predicting overall survival in metastatic breast cancer [J].
Budd, G. Thomas ;
Cristofanilli, Massimo ;
Ellis, Mathew J. ;
Stopeck, Allison ;
Borden, Ernest ;
Miller, M. Craig ;
Matera, Jeri ;
Repollet, Madeline ;
Doyle, Gerald V. ;
Terstappen, Leon W. M. M. ;
Hayes, Daniel F. .
CLINICAL CANCER RESEARCH, 2006, 12 (21) :6403-6409
[7]
CARCINOCYTHEMIA (CARCINOMA CELL LEUKEMIA) - ACUTE LEUKEMIA-LIKE PICTURE DUE TO METASTATIC CARCINOMA CELLS [J].
CAREY, RW ;
TAFT, PD ;
BENNETT, JM ;
KAUFMAN, S .
AMERICAN JOURNAL OF MEDICINE, 1976, 60 (02) :273-278
[8]
Cochran W.G., 1963, SAMPLING TECHNIQUES, V2
[9]
Circulating tumor cells: A novel prognostic factor for newly diagnosed metastatic breast cancer [J].
Cristofanilli, M ;
Hayes, DF ;
Budd, GT ;
Ellis, MJ ;
Stopeck, A ;
Reuben, JM ;
Doyle, GV ;
Matera, J ;
Allard, WJ ;
Miller, MC ;
Fritsche, HA ;
Hortobagyi, GN ;
Terstappen, LWMM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (07) :1420-1430
[10]
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