Circulating Tumor Cells Predict Occult Metastatic Disease and Prognosis in Pancreatic Cancer

被引:91
作者
Court, Colin M. [1 ,2 ,3 ]
Ankeny, Jacob S. [1 ,2 ]
Sho, Shonan [1 ,2 ]
Winograd, Paul [1 ,2 ]
Hou, Shuang [1 ,4 ]
Song, Min [4 ]
Wainberg, Zev A. [5 ]
Girgis, Mark D. [1 ]
Graeber, Thomas G. [3 ,4 ]
Agopian, Vatche G. [1 ]
Tseng, Hsian-Rong [4 ]
Tomlinson, James S. [1 ,2 ,6 ]
机构
[1] Univ Calif Los Angeles, Dept Surg, Los Angeles, CA 90024 USA
[2] Vet Hlth Adm, Dept Surg, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Dept Mol Cellular & Integrat Physiol, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA USA
[5] Univ Calif Los Angeles, Dept Hematol Oncol, Los Angeles, CA USA
[6] Univ Calif Los Angeles, CNSI, Los Angeles, CA 90024 USA
基金
美国国家卫生研究院;
关键词
ADENOCARCINOMA; CHEMOTHERAPY; ENUMERATION; DIAGNOSIS; SURVIVAL; BLOOD;
D O I
10.1245/s10434-017-6290-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Occult metastatic tumors, below imaging thresholds, are a limitation of staging systems that rely on cross-sectional imaging alone and are a cause of the routine understaging of pancreatic ductal adenocarcinomas (PDACs). We investigated circulating tumor cells (CTCs) as a preoperative predictor of occult metastatic disease and as a prognostic biomarker for PDAC patients. A total of 126 patients (100 with cancer, 26 with benign disease) were enrolled in our study and CTCs were identified and enumerated from 4 mL of venous blood using the microfluidic NanoVelcro assay. CTC enumeration was correlated with clinicopathologic variables and outcomes following both surgical and systemic therapies. CTCs were identified in 78% of PDAC patients and CTC counts correlated with increasing stage (rho = 0.42, p < 0.001). Of the 53 patients taken for potentially curative surgery, 13 (24.5%) had occult metastatic disease intraoperatively. Patients with occult disease had significantly more CTCs than patients with local disease only (median 7 vs. 1 CTC, p < 0.0001). At a cut-off of three or more CTCs/4 mL, CTCs correctly identified patients with occult metastatic disease preoperatively (area under the receiver operating characteristic curve 0.82, 95% confidence interval (CI) 0.76-0.98, p < 0.0001). CTCs were a univariate predictor of recurrence-free survival following surgery [hazard ratio (HR) 2.36, 95% CI 1.17-4.78, p = 0.017], as well as an independent predictor of overall survival on multivariate analysis (HR 1.38, 95% CI 1.01-1.88, p = 0.040). CTCs show promise as a prognostic biomarker for PDAC patients at all stages of disease being treated both medically and surgically. Furthermore, CTCs demonstrate potential as a preoperative biomarker for identifying patients at high risk of occult metastatic disease.
引用
收藏
页码:1000 / 1008
页数:9
相关论文
共 22 条
[1]   OPINION Challenges in circulating tumour cell research [J].
Alix-Panabieres, Catherine ;
Pantel, Klaus .
NATURE REVIEWS CANCER, 2014, 14 (09) :623-631
[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]  
Amin M.B., 2017, AM JOINT COMMITTEE C, V8th
[4]   Circulating tumour cells as a biomarker for diagnosis and staging in pancreatic cancer [J].
Ankeny, J. S. ;
Court, C. M. ;
Hou, S. ;
Li, Q. ;
Song, M. ;
Wu, D. ;
Chen, J. F. ;
Lee, T. ;
Lin, M. ;
Sho, S. ;
Rochefort, M. M. ;
Girgis, M. D. ;
Yao, J. ;
Wainberg, Z. A. ;
Muthusamy, V. R. ;
Watson, R. R. ;
Donahue, T. R. ;
Hines, O. J. ;
Reber, H. A. ;
Graeber, T. G. ;
Tseng, H. R. ;
Tomlinson, J. S. .
BRITISH JOURNAL OF CANCER, 2016, 114 (12) :1367-1375
[5]  
[Anonymous], J CLIN ONCOL
[6]   Circulating tumor cells in locally advanced pancreatic adenocarcinoma: the ancillary CirCe 07 study to the LAP 07 trial [J].
Bidard, F. C. ;
Huguet, F. ;
Louvet, C. ;
Mineur, L. ;
Bouche, O. ;
Chibaudel, B. ;
Artru, P. ;
Desseigne, F. ;
Bachet, J. B. ;
Mathiot, C. ;
Pierga, J. Y. ;
Hammel, P. .
ANNALS OF ONCOLOGY, 2013, 24 (08) :2057-2061
[7]   Cutoff Finder: A Comprehensive and Straightforward Web Application Enabling Rapid Biomarker Cutoff Optimization [J].
Budczies, Jan ;
Klauschen, Frederick ;
Sinn, Bruno V. ;
Gyoerffy, Balazs ;
Schmitt, Wolfgang D. ;
Darb-Esfahani, Silvia ;
Denkert, Carsten .
PLOS ONE, 2012, 7 (12)
[8]   Reality of Single Circulating Tumor Cell Sequencing for Molecular Diagnostics in Pancreatic Cancer [J].
Court, Colin M. ;
Ankeny, Jacob S. ;
Sho, Shonan ;
Hou, Shuang ;
Li, Qingyu ;
Hsieh, Carolyn ;
Song, Min ;
Liao, Xinfang ;
Rochefort, Matthew M. ;
Wainberg, Zev A. ;
Graeber, Thomas G. ;
Tseng, Hsian-Rong ;
Tomlinson, James S. .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2016, 18 (05) :688-696
[9]   Improving pancreatic cancer diagnosis using circulating tumor cells: prospects for staging and single-cell analysis [J].
Court, Colin M. ;
Ankeny, Jacob S. ;
Hou, Shuang ;
Tseng, Hsian-Rong ;
Tomlinson, James S. .
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2015, 15 (11) :1491-1504
[10]   Multimarker Gene Analysis of Circulating Tumor Cells in Pancreatic Cancer Patients: A Feasibility Study [J].
de Albuquerque, Andreia ;
Kubisch, Ilja ;
Breier, Georg ;
Stamminger, Gudrun ;
Fersis, Nikos ;
Eichler, Astrid ;
Kaul, Sepp ;
Stoelzel, Ulrich .
ONCOLOGY, 2012, 82 (01) :3-10