Detection of circulating tumor cells in peripheral blood of patients with metastatic breast cancer:: A validation study of the CellSearch system

被引:1063
作者
Riethdorf, Sabine
Fritsche, Herbert
Mueller, Volkmar
Rau, Thomas
Schindibeck, Christian
Rack, Brigitte
Janni, Wolfgang
Coith, Cornelia
Beck, Katrin
Jaenicke, Fritz
Jackson, Summer
Gornet, Terrie
Cristofanilli, Massimo
Pantel, Klaus
机构
[1] Univ Med Ctr Hamburg Eppendorf, Inst Tumor Biol, D-20246 Hamburg, Germany
[2] Univ Med Ctr Hamburg Eppendorf, Inst Pharmacol, D-20246 Hamburg, Germany
[3] Univ Med Ctr Hamburg Eppendorf, Inst Clin Gynecol, D-20246 Hamburg, Germany
[4] Univ Texas, MD Anderson Canc Ctr, Dept Lab Med, Houston, TX 77030 USA
[5] Univ Texas, MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX 77030 USA
[6] Univ Munich, Klinikum Innenstadt, Dept Obstet & Gynecol, D-8000 Munich, Germany
关键词
D O I
10.1158/1078-0432.CCR-06-1695
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The Cell Search system (Veridex, Warren, NJ) is designed to enrich and enumerate circulating tumor cells (CTCs) from peripheral blood. Here, we validated the analytic performance of this system for clinical use in patients with metastatic breast cancer. Experimental Design: This prospective multicenter study conducted at three independent laboratories involved samples from 92 patients with metastatic breast cancer. Intra- and inter-assay variability using controls containing defined numbers of cells (average, 50 and 1,000, respectively), cell stability based on varying storage and shipment conditions, recovery precision from samples spiked with 4 to 12 tumor cells, inter-instrument variability, and positivity of samples from metastatic breast cancer patients were tested. Results: Intra- and inter-assay precision for two sites were high: All eight positive controls analyzed in the same run and >95% of the run to run control values (n = 299) were within the specified ranges. Recovery rate of spiked samples averaged between 80% and 82%. CTCs were detected in similar to 70% of metastatic breast cancer patients. CTC values of identical samples processed either immediately after blood drawing or after storage for 24, 48, or 72 h at room temperature or at 4 degrees C did not differ significantly. Shipment of samples had no influence on CTC values. When analyzing identical samples in different centers, inter-instrument accordance was high. Conclusions: The CellSearch system enables the reliable detection of CTCs in blood and is suitable for the routine assessment of metastatic breast cancer patients in the clinical laboratory. Blood samples should be shipped at room temperature and CTC counts are stable for at least 72 h.
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收藏
页码:920 / 928
页数:9
相关论文
共 40 条
  • [1] Detection and quantification of circulating tumor cells in mouse models of human breast cancer using immunomagnetic enrichment and multiparameter flow cytometry
    Allan, AL
    Vantyghem, SA
    Tuck, AB
    Chambers, AF
    Chin-Yee, IH
    Keeney, M
    [J]. CYTOMETRY PART A, 2005, 65A (01) : 4 - 14
  • [2] Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases
    Allard, WJ
    Matera, J
    Miller, MC
    Repollet, M
    Connelly, MC
    Rao, C
    Tibbe, AGJ
    Uhr, JW
    Terstappen, LWMM
    [J]. CLINICAL CANCER RESEARCH, 2004, 10 (20) : 6897 - 6904
  • [3] Assmann V, 1999, J CELL SCI, V112, P3943
  • [4] Comparison of two methods for enumerating circulating tumor cells in carcinoma patients
    Balic, M
    Dandachi, N
    Hofmann, G
    Samonigg, H
    Loibner, H
    Obwaller, A
    van der Kooi, A
    Tibbe, AGJ
    Doyle, GV
    Terstappen, LWMM
    Bauernhofer, T
    [J]. CYTOMETRY PART B-CLINICAL CYTOMETRY, 2005, 68B (01) : 25 - 30
  • [5] Limitations of specific reverse-transcriptase polymerase chain reaction markers in the detection of metastases in the lymph nodes and blood of breast cancer patients
    Bostick, PJ
    Chatterjee, S
    Chi, DD
    Huynh, KT
    Giuliano, AE
    Cote, R
    Hoon, DSB
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) : 2632 - 2640
  • [6] Cytokeratin-positive cells in the bone marrow and survival of patients with stage I, II, or III breast cancer.
    Braun, S
    Pantel, K
    Muller, P
    Janni, W
    Hepp, F
    Kentenich, CRM
    Gastroph, S
    Wischnik, A
    Dimpfl, T
    Kindermann, G
    Riethmuller, G
    Schlimok, G
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (08) : 525 - 533
  • [7] A pooled analysis of bone marrow micrometastasis in breast cancer
    Braun, S
    Vogl, FD
    Naume, B
    Janni, W
    Osborne, MP
    Coombes, RC
    Schlimok, G
    Diel, IJ
    Gerber, B
    Gebauer, G
    Pierga, JY
    Marth, C
    Oruzio, D
    Wiedswang, G
    Solomayer, EF
    Kundt, G
    Strobl, B
    Fehm, T
    Wong, GYC
    Bliss, J
    Vincent-Salomon, A
    Pantel, K
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (08) : 793 - 802
  • [8] Enrichment methods to detect bone marrow micrometastases in breast carcinoma patients: clinical relevance
    Choesmel, V
    Pierga, JY
    Nos, C
    Vincent-Salomon, A
    Sigal-Zafrani, B
    Thiery, JP
    Blin, N
    [J]. BREAST CANCER RESEARCH, 2004, 6 (05): : R556 - R569
  • [9] Circulating tumor cells: A novel prognostic factor for newly diagnosed metastatic breast cancer
    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
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (07) : 1420 - 1430
  • [10] Circulating tumor cells, disease progression, and survival in metastatic breast cancer
    Cristofanilli, M
    Budd, GT
    Ellis, MJ
    Stopeck, A
    Matera, J
    Miller, MC
    Reuben, JM
    Doyle, GV
    Allard, WJ
    Terstappen, LWMM
    Hayes, DF
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) : 781 - 791