Role of circulating tumor cells and disseminated tumor cells in primary breast cancer

被引:21
作者
Hayashi, Naoki [1 ,2 ,3 ]
Yamauchi, Hideko [1 ]
机构
[1] St Lukes Int Hosp, Dept Breast Surg Oncol, Chuo Ku, Tokyo 1048560, Japan
[2] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX 77030 USA
[3] Showa Univ, Dept Pathol 2, Sch Med, Shinagawa Ku, Tokyo 1428555, Japan
关键词
Circulating tumor cells; Disseminated tumor cells; Breast neoplasm; Metastasis; BONE-MARROW MICROMETASTASES; REVERSE TRANSCRIPTION-PCR; POLYMERASE-CHAIN-REACTION; PERIPHERAL-BLOOD; PROGNOSTIC VALUE; ADJUVANT CHEMOTHERAPY; MOLECULAR-DETECTION; AMERICAN-SOCIETY; PRIMARY SURGERY; POOLED ANALYSIS;
D O I
10.1007/s12282-011-0282-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastasis remains a main cause of death in patients with breast cancer regardless of improvements in treatment. Prospective clinical studies of this minimal residual disease have shown disseminated tumor cells (DTCs) in bone marrow and circulating tumor cells (CTCs) in peripheral blood, neither of which can be detected by conventional imaging, to be prognostic and predictive markers for responsive treatment in patients with metastatic breast cancer. However, the guideline from the American Society of Clinical Oncology does not recommend measuring CTCs for clinical decisions because of a lack of evidence for an established, sound methodology and with proven clinical relevance. The Southwest Oncology Group trial S0500 to validate the clinical relevance of CTCs for treatment decisions in patients with metastatic breast cancer is ongoing. In patients with primary breast cancer, the low detection rate of CTCs has been overcome by recent advances in technology. Although generally DTCs were more detectable than CTCs and the association between presence of DTCs and poor prognosis has been shown, the invasiveness of sample collection of DTCs from bone marrow is generally hard for patients to accept. In this review, we concentrate on the question of whether we need to consider CTCs and DTCs in the management of primary breast cancer on the basis of the evidence of the clinical relevance of CTCs and DTCs. The promising role of the molecular characterization of CTCs, which does have the potential for being a predictor for tumor behavior and development, is suggested as a new targeting strategy.
引用
收藏
页码:110 / 117
页数:8
相关论文
共 59 条
[1]   Stem cell and epithelial-mesenchymal transition markers are frequently overexpressed in circulating tumor cells of metastatic breast cancer patients [J].
Aktas, Bahriye ;
Tewes, Mitra ;
Fehm, Tanja ;
Hauch, Siegfried ;
Kimmig, Rainer ;
Kasimir-Bauer, Sabine .
BREAST CANCER RESEARCH, 2009, 11 (04)
[2]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[3]   Current status in human breast cancer micrometastasis [J].
Alix-Panabieres, Catherine ;
Mueller, Volkmar ;
Pantel, Klaus .
CURRENT OPINION IN ONCOLOGY, 2007, 19 (06) :558-563
[4]   Most early disseminated cancer cells detected in bone marrow of breast cancer patients have a putative breast cancer stem cell phenotype [J].
Balic, Marija ;
Lin, Henry ;
Young, Lillian ;
Hawes, Debra ;
Giuliano, Armando ;
McNamara, George ;
Datar, Ram H. ;
Cote, Richard J. .
CLINICAL CANCER RESEARCH, 2006, 12 (19) :5615-5621
[5]   Effect of different cytokines on mammaglobin and maspin gene expression in normal leukocytes: possible relevance to the assays for the detection of micrometastatic breast cancer [J].
Ballestrero, A ;
Garuti, A ;
Bertolotto, M ;
Rocco, I ;
Boy, D ;
Nencioni, A ;
Ottonello, L ;
Patrone, F .
BRITISH JOURNAL OF CANCER, 2005, 92 (10) :1948-1952
[6]   Prognostic value of monitoring tumour markers CA 15-3 and CEA during fulvestrant treatment [J].
Bartsch, R ;
Wenzel, C ;
Pluschnig, U ;
Hussian, D ;
Sevelda, U ;
Altorjai, G ;
Locker, GJ ;
Mader, R ;
Zielinski, CC ;
Steger, GG .
BMC CANCER, 2006, 6 (1)
[7]   Time is an important factor when processing samples for the detection of disseminated tumor cells in blood/bone marrow by reverse transcription-PCR [J].
Becker, S ;
Becker-Pergola, G ;
Fehm, T ;
Wallwiener, D ;
Solomayer, EF .
CLINICAL CHEMISTRY, 2004, 50 (04) :785-786
[8]   Molecular detection of cancer cells in bone marrow and peripheral blood of patients with operable breast cancer.: Comparison of CK19, MUC1 and CEA using RT-PCR [J].
Berois, N ;
Varangot, M ;
Aizen, B ;
Estrugo, R ;
Zarantonelli, L ;
Fernández, P ;
Krygier, G ;
Simonet, F ;
Barrios, E ;
Musé, L ;
Osinaga, E .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (06) :717-723
[9]   Single circulating tumor cell detection and overall survival in nonmetastatic breast cancer [J].
Bidard, F. -C. ;
Mathiot, C. ;
Delaloge, S. ;
Brain, E. ;
Giachetti, S. ;
de Cremoux, P. ;
Marty, M. ;
Pierga, J. -Y. .
ANNALS OF ONCOLOGY, 2010, 21 (04) :729-733
[10]   Cytokeratin-positive cells in the bone marrow and survival of patients with stage I, II, or III breast cancer. [J].
Braun, S ;
Pantel, K ;
Muller, P ;
Janni, W ;
Hepp, F ;
Kentenich, CRM ;
Gastroph, S ;
Wischnik, A ;
Dimpfl, T ;
Kindermann, G ;
Riethmuller, G ;
Schlimok, G .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (08) :525-533