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
[1]   Specific P53 mutations are associated with de novo resistance to doxorubicin in breast cancer patients [J].
Aas, T ;
Borresen, AL ;
Geisler, S ;
SmithSorensen, B ;
Johnsen, H ;
Varhaug, JE ;
Akslen, LA ;
Lonning, PE .
NATURE MEDICINE, 1996, 2 (07) :811-814
[2]  
Abe O, 1998, LANCET, V352, P930
[3]   ASSOCIATION OF P53 PROTEIN EXPRESSION WITH TUMOR-CELL PROLIFERATION RATE AND CLINICAL OUTCOME IN NODE-NEGATIVE BREAST-CANCER [J].
ALLRED, DC ;
CLARK, GM ;
ELLEDGE, R ;
FUQUA, SAW ;
BROWN, RW ;
CHAMNESS, GC ;
OSBORNE, CK ;
MCGUIRE, WL .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (03) :200-206
[4]   Primary chemotherapy in operable breast cancer: Eight-year experience at the Milan Cancer Institute [J].
Bonadonna, G ;
Valagussa, P ;
Brambilla, C ;
Ferrari, L ;
Moliterni, A ;
Terenziani, M ;
Zambetti, M .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (01) :93-100
[5]   Predictors of local-regional recurrence after neoadjuvant chemotherapy and mastectomy without radiation [J].
Buchholz, TA ;
Tucker, SL ;
Masullo, L ;
Kuerer, HM ;
Erwin, J ;
Salas, J ;
Frye, D ;
Strom, EA ;
McNeese, MD ;
Perkins, G ;
Katz, A ;
Singletary, SE ;
Hunt, KK ;
Buzdar, AU ;
Hortobagyi, GN .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (01) :17-23
[6]   Biologic markers as predictors of clinical outcome from systemic therapy for primary operable breast cancer [J].
Chang, J ;
Powles, TJ ;
Allred, DC ;
Ashey, SE ;
Clark, GM ;
Makris, A ;
Assersohn, L ;
Gregory, RK ;
Osborne, CK ;
Dowsett, M .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (10) :3058-3063
[7]   Response to primary chemotherapy in breast cancer patients with tumors not expressing estrogen and progesterone receptors [J].
Colleoni, M ;
Minchella, I ;
Mazzarol, G ;
Nolè, F ;
Peruzzotti, G ;
Rocca, A ;
Viale, G ;
Orlando, L ;
Ferretti, G ;
Curigliano, G ;
Veronesi, P ;
Intra, M ;
Goldhirsch, A .
ANNALS OF ONCOLOGY, 2000, 11 (08) :1057-1059
[8]  
Daidone MG, 1999, INT J CANCER, V84, P580, DOI 10.1002/(SICI)1097-0215(19991222)84:6<580::AID-IJC7>3.0.CO
[9]  
2-W
[10]   CHANGES IN BIOLOGICAL MARKERS AFTER PRIMARY CHEMOTHERAPY FOR BREAST CANCERS [J].
DAIDONE, MG ;
SILVESTRINI, R ;
LUISI, A ;
MASTORE, M ;
BENINI, E ;
VENERONI, S ;
BRAMBILLA, C ;
FERRARI, L ;
GRECO, M ;
ANDREOLA, S ;
VERONESI, U .
INTERNATIONAL JOURNAL OF CANCER, 1995, 61 (03) :301-305