Detection of isolated tumor cells in peripheral blood and in BM: evaluation of a new enrichment method

被引:55
作者
Naume, B [1 ]
Borgen, E
Tossvik, S
Pavlak, N
Oates, D
Nesland, JM
机构
[1] Univ Oslo, Norwegian Radium Hosp, Dept Oncol, NO-0310 Oslo, Norway
[2] Univ Oslo, Norwegian Radium Hosp, Dept Pathol, NO-0310 Oslo, Norway
[3] Appl Imaging Corp, Santa Clara, CA USA
关键词
isolated tumor cells; enrichment; peripheral blood; bone marrow; carcinoma patients;
D O I
10.1080/14653240410006086
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Cell enrichment methods that deal with larger volumes of peripheral blood and BM are needed for increased sensitivity of detection, characterization and quantification of isolated tumor cells (ITC). This study was designed to evaluate a new procedure, the RosetteSep-Applied Imaging Rare Event (RARE) detection method, which depletes the majority of the erythrocytes and leucocytes in a peripheral blood (PB) sample, thereby negatively enriching tumor cells if present. This enrichment procedure allows for increased sensitivity, by analyzing a 5-10 fold larger volume of blood, compared with a direct immunocytochemical (ICC) technique, with minimal impact on laboratory workload. Model experiments showed comparable tumor cell recoveries between the two tested methods, both in PB and BM. Clinical samples were evaluated using paired PB and BM samples from 95 carcinoma patients. Analysis of PB results showed that 25.3% had greater than or equal to 1 tumor cell detected by the RARE procedure, compared with 5.2% after direct ICC analysis, analyzing a 10-fold larger volume by the RARE procedure. The direct ICC analysis of BM from the same patients revealed 16.8% positive. The ITC detection differed both quantitatively and qualitatively between BM and PB, as samples with high numbers of ITC in BM were still negative in PB. The clinical significance of ITC in blood still needs to be established. However, the easy access of peripheral blood, and the increased sensitivity obtained by increasing the sample volume with the RARE procedure, suggests that the value of peripheral blood analysis should be tested in parallel in studies where ITC detection in BM is performed.
引用
收藏
页码:244 / 252
页数:9
相关论文
共 27 条
  • [1] A real-time quantitative reverse transcriptase polymerase chain reaction (RT-PCR) to detect breast carcinoma cells in peripheral blood
    Aerts, J
    Wynendaele, W
    Paridaens, R
    Christiaens, MR
    van den Bogaert, W
    van Oosterom, AT
    Vandekerckhove, F
    [J]. ANNALS OF ONCOLOGY, 2001, 12 (01) : 39 - 46
  • [2] Standardization of the immunocytochemical detection of cancer cells in BM and blood: I. establishment of objective criteria for the evaluation of immunostained cells
    Borgen, E
    Naume, B
    Nesland, JM
    Kvalheim, G
    Beiske, K
    Fodstad, O
    Diel, I
    Solomayer, EF
    Theocharous, P
    Coombes, RC
    Smith, BM
    Wunder, E
    Marolleau, JP
    Garcia, J
    Pantel, K
    [J]. CYTOTHERAPY, 1999, 1 (05) : 377 - 388
  • [3] Borgen E, 1998, J PATHOL, V185, P427, DOI 10.1002/(SICI)1096-9896(199808)185:4<427::AID-PATH127>3.0.CO
  • [4] 2-7
  • [5] Brandt B, 1996, CANCER RES, V56, P4556
  • [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] PREDICTION OF EARLY RELAPSE IN PATIENTS WITH OPERABLE BREAST-CANCER BY DETECTION OF OCCULT BONE-MARROW MICROMETASTASES
    COTE, RJ
    ROSEN, PP
    LESSER, ML
    OLD, LJ
    OSBORNE, MP
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (10) : 1749 - 1756
  • [8] Denis MG, 1997, INT J CANCER, V74, P540, DOI 10.1002/(SICI)1097-0215(19971021)74:5<540::AID-IJC11>3.0.CO
  • [9] 2-A
  • [10] Micrometastatic breast cancer cells in bone marrow at primary surgery: Prognostic value in comparison with nodal
    Diel, IJ
    Kaufmann, M
    Costa, SD
    Holle, R
    vonMinckwitz, G
    Solomayer, EF
    Kaul, S
    Bastert, G
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (22): : 1652 - 1658