Molecular profiling and predictive value of circulating tumor cells in patients with metastatic breast cancer: an option for monitoring response to breast cancer related therapies

被引:158
作者
Tewes, Mitra [2 ]
Aktas, Bahriye [1 ]
Welt, Anja [2 ]
Mueller, Siemke [3 ]
Hauch, Siegfried [4 ]
Kimmig, Rainer [1 ]
Kasimir-Bauer, Sabine [1 ]
机构
[1] Univ Duisburg Essen, Dept Gynecol & Obstet, Univ Hosp Essen, D-45122 Essen, Germany
[2] Univ Duisburg Essen, Dept Internal Med Canc Res, Univ Hosp Essen, D-45122 Essen, Germany
[3] Kath Marienkrankenhaus GmbH, Zentrum Innere Med, D-22087 Hamburg, Germany
[4] AdnaGen AG, D-30853 Langenhagen, Germany
关键词
Circulating tumor cells; Molecular profiling; Therapy monitoring; Metastatic breast cancer; TIME RT-PCR; BONE-MARROW; PERIPHERAL-BLOOD; ADJUVANT CHEMOTHERAPY; CLINICAL-SIGNIFICANCE; DIFFERENTIAL EXPRESSION; COLORECTAL-CANCER; EPITHELIAL-CELLS; HIGH-RISK; RECOMMENDATIONS;
D O I
10.1007/s10549-008-0143-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose We analyzed circulating tumor cells (CTC) in blood of metastatic breast cancer patients (n = 42) and determined the ability of this method to predict therapy response. Methods CTC from blood were analyzed before and during therapy for EpCAM, MUC1 and HER2 transcripts with the AdnaTest BreastCancer. The estrogen (ER) and progesterone (PR) receptor expression was assessed by RT-PCR. Results The overall detection rate for CTC was 52% (thereof 86% EpCAM; 86% MUC1; 32% HER2; 35% ER; 12% PR). CTC were ER, PR and HER2 negative in 45% (ER), 78% (PR) and 60% (HER-2) of patients with steroid receptor-positive tumors. 29% of patients with HER2-negative tumors had HER2-positive CTC. The test predicted therapy response in 78% of all cases. Persistence of CTC significantly correlated with shorter overall survival (P = 0.005). Conclusions Molecular profiling of CTC may offer superior prognostic information with regard to risk assessment for recurrence and predictive judgement of therapeutical regimens.
引用
收藏
页码:581 / 590
页数:10
相关论文
共 41 条
  • [1] Baker MK, 2003, CLIN CANCER RES, V9, P4865
  • [2] 2000 update of recommendations for the use of tumor markers in breast and colorectal cancer: Clinical practice guidelines of the American Society of Clinical Oncology
    Bast, RC
    Ravdin, P
    Hayes, DF
    Bates, S
    Fritsche, H
    Jessup, JM
    Kemeny, N
    Locker, GY
    Mennel, RG
    Somerfield, MR
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (06) : 1865 - 1878
  • [3] Becker S, 2005, ANTICANCER RES, V25, P2171
  • [4] Real- time RT-PCR detection of disseminated tumour cells in bone marrow has superior prognostic significance in comparison with circulating tumour cells in patients with breast cancer
    Benoy, IH
    Elst, H
    Philips, M
    Wuyts, H
    Van Dam, P
    Scharpé, S
    Van Marck, E
    Vermeulen, PB
    Dirix, LY
    [J]. BRITISH JOURNAL OF CANCER, 2006, 94 (05) : 672 - 680
  • [5] Bosma AJ, 2002, CLIN CANCER RES, V8, P1871
  • [6] Braun S, 1999, INT J CANCER, V84, P1, DOI 10.1002/(SICI)1097-0215(19990219)84:1<1::AID-IJC1>3.0.CO
  • [7] 2-A
  • [8] Braun S, 2001, CANCER RES, V61, P1890
  • [9] 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
  • [10] Lack of effect of adjuvant chemotherapy on the elimination of single dormant tumor cells in bone marrow of high-risk breast cancer patients
    Braun, S
    Kentenich, C
    Janni, W
    Hepp, F
    de Waal, J
    Willgeroth, F
    Sommer, H
    Pantel, K
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (01) : 80 - 86