Clinical Significance of Circulating Tumor Microemboli as a Prognostic Marker in Patients with Pancreatic Ductal Adenocarcinoma

被引:88
作者
Chang, Ming-Chu [1 ]
Chang, Yu-Ting [1 ]
Chen, Jia-Yang [2 ]
Jeng, Yung-Ming [3 ]
Yang, Ching-Yao [4 ]
Tien, Yu-Wen [4 ]
Yang, Shih-Hung [5 ]
Chen, Huai-Lu [2 ]
Liang, Ting-Yuan [2 ]
Wang, Chien-Fang [2 ]
Lee, Eva Y. H. P. [6 ]
Chang, Ying-Chih [2 ]
Lee, Wen-Hwa [2 ,7 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[2] Acad Sinica, Genom Res Ctr, 128 Acad Rd,Sect 2, Taipei 11529, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Pathol, Taipei 100, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Surg, Taipei 100, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Oncol, Taipei, Taiwan
[6] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92717 USA
[7] China Med Univ, Taiwan Grad Inst Clin Med, Taichung, Taiwan
关键词
CELL LUNG-CANCER; RT-PCR; CARCINOMA PATIENTS; BREAST-CANCER; METASTASIS; SURVIVAL; DISSEMINATION; PROGRESSION; TRANSITION; BIOMARKER;
D O I
10.1373/clinchem.2015.248260
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
100118 [医学信息学]; 100208 [临床检验诊断学];
摘要
BACKGROUND: Characterization of circulating tumor cells (CTCs) has been used to provide prognostic, predictive, and pharmacodynamic information in many different cancers. However, the clinical significance of CTCs and circulating tumor microemboli (CTM) in patients with pancreatic ductal adenocarcinoma (PDAC) has yet to be determined. METHODS: In this prospective study, CTCs and CTM were enumerated in the peripheral blood of 63 patients with PDAC before treatment using anti-EpCAM (epithelial cell adhesion molecule)-conjugated supported lipid bilayer-coated microfluidic chips. Associations of CTCs and CTM with patients' clinical factors and prognosis were determined. RESULTS: CTCs were abundant [mean (SD), 70.2 (107.6)] and present in 81% (51 of 63) of patients with PDAC. CTM were present in 81% (51 of 63) of patients with mean (SD) 29.7 (1101.4). CTM was an independent prognostic factor of overall survival (OS) and progression free survival (PFS). Patients were stratified into unfavorable and favorable CTM groups on the basis of CTM more or less than 30 per 2 mL blood, respectively. Patients with baseline unfavorable CTM, compared with patients with favorable CTM, had shorter PFS (2.7 vs 12.1 months; P < 0.0001) and OS (6.4 vs 19.8 months; P < 0.0001). Differences persisted if we stratified patients into early and advanced diseases. The number of CTM before treatment was an independent predictor of PFS and OS after adjustment for clinically significant factors. CONCLUSIONS: The number of CTM, instead of CTCs, before treatment is an independent predictor of PFS and OS in patients with PDAC. (C) 2015 American Association for Clinical Chemistry
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收藏
页码:505 / 513
页数:9
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