Assessment of circulating tumor cells and serum markers for progression-free survival prediction in metastatic breast cancer: a prospective observational study

被引:72
作者
Bidard, Francois-Clement [1 ,2 ]
Hajage, David [3 ]
Bachelot, Thomas [4 ]
Delaloge, Suzette [5 ]
Brain, Etienne [6 ]
Campone, Mario [7 ]
Cottu, Paul [1 ]
Beuzeboc, Philippe [1 ]
Rolland, Emilie [3 ]
Mathiot, Claire [8 ]
Pierga, Jean-Yves [1 ,2 ]
机构
[1] Inst Curie, Dept Med Oncol, F-75005 Paris, France
[2] Univ Paris 05, F-75006 Paris, France
[3] Inst Curie, Dept Biostat, F-75005 Paris, France
[4] Ctr Leon Berard, Dept Med Oncol, F-69008 Lyon, France
[5] Inst Gustave Roussy, Dept Med Oncol, F-94800 Villejuif, France
[6] Hop Rene Huguenin, Dept Med Oncol, Inst Curie, F-92210 St Cloud, France
[7] Inst Cancerol Ouest, Dept Med Oncol, F-44800 St Herblain, France
[8] Inst Curie, Hematol Lab, F-75005 Paris, France
来源
BREAST CANCER RESEARCH | 2012年 / 14卷 / 01期
关键词
CARCINOEMBRYONIC ANTIGEN; CYTOKERATIN-19; FRAGMENT; AMERICAN-SOCIETY; CYFRA-21-1; RECOMMENDATIONS; CA-15.3; UPDATE;
D O I
10.1186/bcr3114
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Introduction: Circulating tumor cells (CTC) have been recently proposed as a new dynamic blood marker whose positivity at baseline is a prognostic factor and whose changes under treatment are correlated with progression-free survival (PFS) in metastatic breast cancer patients. However, serum marker levels are also used for the same purpose, and no clear comparison has been reported to date. Methods: The IC 2006-04 enrolled prospectively 267 metastatic breast cancer patients treated by first line chemotherapy and confirmed that CTC levels are an independent prognostic factor for PFS and overall survival (OS). A secondary pre-planned endpoint was to compare prospectively the positivity rates and the value of CTC (CellSearch (R)), of serum tumor markers (carcinoembryonic antigen (CEA), cancer antigen 15.3 (CA 15-3), CYFRA 21-1), and of serum non-tumor markers (lactate deshydrogenase (LDH), alkaline phosphatase (ALP)) at baseline and under treatment for PFS prediction, independently from the other known prognostic factors, using univariate analyses and concordance indexes. Results: A total of 90% of the patients had at least one elevated blood marker. Blood markers were correlated with poor performance status, high number of metastatic sites and with each other. In particular, CYFRA 21-1, a marker usually used in lung cancer, was elevated in 65% of patients. A total of 86% of patients had either CA 15-3 and/or CYFRA 21-1 elevated at baseline. Each serum marker was associated, when elevated at baseline, with a significantly shorter PFS. Serum marker changes during treatment, assessed either between baseline and week 3 or between baseline and weeks 6 to 9, were significantly associated with PFS, as reported for CTC. Concordance indexes comparison showed no clear superiority of any of the serum marker or CTC for PFS prediction. Conclusions: For the purpose of PFS prediction by measuring blood marker changes during treatment, currently available blood-derived markers (CTC and serum markers) had globally similar performances. Besides CEA and CA 15-3, CYFRA 21-1 is commonly elevated in metastatic breast cancer and has a strong prognostic value.
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页数:10
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