The role of biological markers as predictors of response to preoperative chemotherapy in large primary breast cancer

被引:15
作者
Cocquyt, VF
Schelfhout, VR
Blondeel, PN
Depypere, HT
Daems, KK
Serreyn, RF
Praet, MM
Van Belle, SJP
机构
[1] State Univ Ghent Hosp, Dept Med Oncol, B-9000 Ghent, Belgium
[2] State Univ Ghent Hosp, N Goormaghtigh Inst Pathol, B-9000 Ghent, Belgium
[3] State Univ Ghent Hosp, Dept Plast & Reconstruct Surg, B-9000 Ghent, Belgium
[4] State Univ Ghent Hosp, Dept Gynaecol, B-9000 Ghent, Belgium
[5] AstraZeneca, Biostatician, Macclesfield, Cheshire, England
关键词
breast cancer; preoperative chemotherapy; biological markers;
D O I
10.1385/MO:20:3:221
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this prospective study was to evaluate biological markers, their correlation with response and outcome, and the change in these markers under the influence of preoperative chemotherapy (PCT) in patients with a large primary breast cancer. One hundred and thirty-five women were treated with PCT, followed by locoregional therapy and adjuvant treatment. Estrogen receptor (ER), progesterone receptor (PgR), HER-2, p53, and cathepsin D were determined by immunohistochemistry (IHC) before and after PCT. The overall response (OR) was 70% and the pathologic complete response (pCR) was 13%. Forty-four percent of the patients could be offered breast-conserving surgery (BCS). At a median follow-up of 50 mo the overall survival is 82% and the disease-free survival is 70%. No local recurrence (LR) has developed following BCS. Invasive ductal carcinoma (IDC) was more frequently ER-negative and HER-2-positive than invasive lobular carcinoma (ILC). P53-negative and ER-negative patients seemed to be more chemosensitive compared to p53-positive patients (74% vs 53%) and ER-positive patients (75% vs 65%), but this difference did not reach statistical significance. A trend toward higher complete pathologic remission rate was seen for ER-negative patients (p 0.0609). PgR, HER-2, and cathepsin D were not related to response. The pattern of biological markers did not change with PCT, making repeated determination useless.
引用
收藏
页码:221 / 231
页数:11
相关论文
共 36 条
[21]   Comparison of fluorescence in situ hybridization and immunohistochemistry for the evaluation of HER-2/neu in breast cancer [J].
Jacobs, TW ;
Gown, AM ;
Yaziji, H ;
Barnes, MJ ;
Schnitt, SJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (07) :1974-1982
[22]   Clinical course of breast cancer patients with complete pathologic primary tumor and axillary lymph node response to doxorubicin-based neoadjuvant chemotherapy [J].
Kuerer, HM ;
Newman, LA ;
Smith, TL ;
Ames, FC ;
Hunt, KK ;
Dhingra, K ;
Theriault, RL ;
Singh, G ;
Binkley, SM ;
Sneige, N ;
Buchholz, TA ;
Ross, MI ;
McNeese, MD ;
Buzdar, AU ;
Hortobagyi, GN ;
Singletary, SE .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (02) :460-469
[23]   Randomized trial of intensive cyclophosphamide, epirubicin, and fluorouracil chemotherapy compared with cyclophosphamide, methotrexate, and fluorouracil in premenopausal women with node-positive breast cancer [J].
Levine, MN ;
Bramwell, VH ;
Pritchard, KI ;
Norris, BD ;
Shepherd, LE ;
Abu-Zahra, H ;
Findlay, B ;
Warr, D ;
Bowman, D ;
Myles, J ;
Arnold, A ;
Vandenberg, T ;
MacKenzie, R ;
Robert, J ;
Ottaway, J ;
Burnell, M ;
Williams, CK ;
Tu, DS .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) :2651-2658
[24]   Primary chemotherapy in breast invasive carcinoma: Predictive value of the immunohistochemical detection of hormonal receptors, p53, c-erbB-2, MiB1, pS2 and GST pi [J].
MacGrogan, G ;
Mauriac, L ;
Durand, M ;
Bonichon, F ;
Trojani, M ;
deMascarel, I ;
Coindre, JM .
BRITISH JOURNAL OF CANCER, 1996, 74 (09) :1458-1465
[25]  
Makris A, 1997, CLIN CANCER RES, V3, P593
[26]   INTERACTIONS OF CATHEPSIN-D AND INSULIN-LIKE GROWTH FACTOR-II (IGF-II) ON THE IGF-II MANNOSE-6-PHOSPHATE RECEPTOR IN HUMAN BREAST-CANCER CELLS AND POSSIBLE CONSEQUENCES ON MITOGENIC ACTIVITY OF IGF-II [J].
MATHIEU, M ;
ROCHEFORT, H ;
BARENTON, B ;
PREBOIS, C ;
VIGNON, F .
MOLECULAR ENDOCRINOLOGY, 1990, 4 (09) :1327-1335
[27]   C-ERBB-2 EXPRESSION AND RESPONSE TO ADJUVANT THERAPY IN WOMEN WITH NODE-POSITIVE EARLY BREAST-CANCER [J].
MUSS, HB ;
THOR, AD ;
BERRY, DA ;
KUTE, T ;
LIU, ET ;
KOERNER, F ;
CIRRINCIONE, CT ;
BUDMAN, DR ;
WOOD, WC ;
BARCOS, M ;
HENDERSON, IC .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (18) :1260-1266
[28]   Predictive value of c-erbB-2, p53, cathepsin-D and histology of the primary tumour in metastatic breast cancer [J].
Niskanen, E ;
Blomqvist, C ;
Franssila, K ;
Hietanen, P ;
Wasenius, VM .
BRITISH JOURNAL OF CANCER, 1997, 76 (07) :917-922
[29]   BIOLOGICAL AND CLINICAL-SIGNIFICANCE OF CATHEPSIN-D IN BREAST-CANCER [J].
ROCHEFORT, H .
ACTA ONCOLOGICA, 1992, 31 (02) :125-130
[30]  
Rozan S, 1998, INT J CANCER, V79, P27, DOI 10.1002/(SICI)1097-0215(19980220)79:1<27::AID-IJC6>3.0.CO