The Use of a New CellCollector to Isolate Circulating Tumor Cells from the Blood of Patients with Different Stages of Prostate Cancer and Clinical Outcomes - A Proof-of-Concept Study

被引:48
|
作者
Theil, Gerit [1 ]
Fischer, Kersten [1 ]
Weber, Ekkehard [2 ]
Medek, Rita [3 ]
Hoda, Raschid [1 ,4 ]
Luecke, Klaus [2 ]
Fornara, Paolo [1 ]
机构
[1] Univ Halle Wittenberg, Clin Urol & Transplantat, Ernst Grube Str 40, D-06120 Halle, Germany
[2] GILUPI GmbH, Muhlenberg 11, Potsdam, Germany
[3] Univ Halle Wittenberg, Inst Physiol Chem, Hollystr 1, D-06120 Halle, Germany
[4] Univ Klinikum Schleswig Holstein, Urol Clin, Ratzburger Allee 160, D-23538 Lubeck, Germany
来源
PLOS ONE | 2016年 / 11卷 / 08期
关键词
PERIPHERAL-BLOOD; PREDICT SURVIVAL; CTC; ABIRATERONE; EXPERIENCE; CARCINOMA; DISEASES;
D O I
10.1371/journal.pone.0158354
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background and Methods Circulating tumor cells (CTCs) constitute a useful approach for personalized medicine. Nevertheless, the isolation of these cells remains very challenging because they rarely circulate in the blood. Another current problem is the cancer-specific characterization of these cells, which requires a method that allows for the molecular and immunocytochemical profiling of all captured cells. The purpose of our proof of concept study was to investigate the use of a medical wire (CellCollector, GILUPI) to isolate CTCs in the blood of prostate cancer (PCa) patients, which allowed CTCs to be counted and molecularly characterized. Forty-three PCa patients in different stages and 11 control subjects were studied. Some randomized samples were used to detect tumor-associated transcripts, such as prostate-specific membrane antigen (PSMA), prostate-specific antigen (PSA) and epidermal growth factor receptor (EGFR), in the isolated CTCs. Results The mean CTC counts were 4.6 CTCs [range, 0-8] in patients with localized PCa, 16.8 CTCs [range, 10-25] in patients with locally advanced PCa, and 26.8 CTCs [range, 0-98] in patients with metastatic PCa. The median follow-up time was 24 months, and there was a significant difference in the cancer-specific survival rates. Patients with CTC counts under 5 CTCs lived significantly longer (p = 0.035) than patients with more than 5 CTCs. We also demonstrated that the captured CTCs could be molecularly characterized. We detected tumor-associated transcripts of EGFR and PSMA in patients with metastatic PCa in 42.8% and 14.3% of the analyzed samples, respectively. Conclusion Our results indicate that the sensitive isolation and molecular characterization of CTCs can be achieved ex vivo using the wire. Patients with more than 5 CTCs had a mortality risk that was 7.0 times greater that of those with fewer than 5 CTCs (hazard ratio 7.0 95%, CI 1.1-29.39). This proof of concept was required for the approval of the use of the CellCollector in a clinical study for the in vivo isolation of CTCs from the blood stream of PCa patients by the Federal Institute for Drugs and Medical devices (Germany, BfArM).
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页数:14
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