C-erbB-2 expression does not predict response to docetaxel or sequential methotrexate and 5-fluorouracil in advanced breast cancer

被引:39
作者
Sjöström, J
Collan, J
von Boguslawski, K
Franssila, K
Bengtsson, NO
Mjaaland, I
Malmström, P
Ostenstad, B
Wist, E
Valvere, V
Bergh, J
Skiöld-Petterson, D
Saksela, E
Blomqvist, C
机构
[1] Univ Helsinki Hosp, Dept Oncol, FIN-00290 Helsinki, Finland
[2] Univ Helsinki Hosp, Dept Pathol, FIN-00290 Helsinki, Finland
[3] Umea Univ Hosp, Dept Oncol, S-90185 Umea, Sweden
[4] Cent Hosp Rogaland, Dept Oncol, Stavanger, Norway
[5] Univ Lund Hosp, Dept Oncol, S-22185 Lund, Sweden
[6] Ulleval Hosp, Dept Oncol, N-0407 Oslo, Norway
[7] Univ Tromso Hosp, Dept Oncol, Tromso, Norway
[8] Karolinska Hosp, Dept Oncol, S-10401 Stockholm, Sweden
[9] Danderyd Hosp, Dept Oncol, Stockholm, Sweden
[10] Univ Uppsala Hosp, Dept Oncol, S-75185 Uppsala, Sweden
关键词
breast cancer; c-erbB-2; chemotherapy; docetaxel; predictive factor;
D O I
10.1016/S0959-8049(01)00403-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer patients with c-erbB-2-positive tumours seem to benefit from anthracycline-based adjuvant chemotherapy. The predictive value of c-erbB-2 for taxane sensitivity is not yet clear. The purpose of this study was to assess whether c-erbB-2 expression is associated with clinical sensitivity to docetaxel (T) or sequential methotrexate and 5-fluorouracil (MF). A total of 283 patients with metastatic breast cancer were initially enrolled in a randomised multicentre trial comparing docetaxel with sequential MF in advanced breast cancer. Paraffin-embedded blocks of the primary tumour were available for 131 patients (46%). c-erbB-2 status was determined by immunohistochemistry using a polyclonal antibody to the c-erbB-2 protein. C-erbB-2 expression was scored in a semi-quantitative fashion using a 0 to 3+ scale. Staining scores 2+ or greater were considered positive, Response evaluation was performed according to World Health Organization (WHO) recommendations. Overall 54 (42%) patients had c-erbB-2-positive tumours. There was no association between treatment outcome and c-erbB-2 overexpression. The overall response rates (RR) (n = 128) among c-erbB-2 -negative and -positive patients were 35 and 44%, respectively (P=0.359). In the MF arm (n = 62), the RR was somewhat higher in the c-erbB-.2 overexpressors (33% versus 18%, P = 0. 18). In the docetaxel arm the RRs were very similar, regardless of the c-erbB-2 expression (53% versus 53%). While several studies have suggested a prognostic and putative predictive significance of c-erbB-2 overexpression in early breast cancer, the significance of c-erbB-2 expression as a predictive factor for response to various cytotoxic treatments in advanced breast cancer is still controversial. In this study, c-erbB-2 expression could not predict response to either MF or T. Thus, tumours over-expressing c-erbB-2 are not uniformly more sensitive to taxanes and c-erbB-2 expression cannot yet be applied clinically as a predictive factor for response in advanced breast cancer. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:535 / 542
页数:8
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