Prognostic value of the quantitative measurement of the oncoprotein p185Her-2/neu in a group of patients with breast cancer and positive node involvement

被引:7
作者
Bohn, U
Aguiar, J
Bilbao, C
Murias, A
Vega, V
Chirino, R
Díaz-Chico, N
Díaz-Chico, JC
机构
[1] Hosp Gen Gran Canaria Dr Negrin, Serv Oncol Med, Las Palmas Gran Canaria 35020, Spain
[2] Hosp Univ Insular Gran Canaria, Med Oncol Serv, Las Palmas Gran Canaria, Spain
[3] Hosp Univ Insular Gran Canaria, Serv Cirugia, Las Palmas Gran Canaria, Spain
[4] Univ Las Palmas de Gran Canaria, Dept Endocrinol Celular & Mol, Las Palmas Gran Canaria, Spain
关键词
breast cancer; p185; oncoprotein; ELISA;
D O I
10.1002/ijc.10612
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Our study attempts to determine the prognostic value of the quantitative measurement of the oncoprotein p185(Her-2/neu) in a group of patients with breast cancer and positive node involvement. In a series of 217 patients with breast cancer and positive nodes in whom the oncoprotein p185 was quantitatively determined by ELISA, we analyzed the clinicopathological variables including age, menopausal status, tumor size, number of affected nodes, type and histology grade and the molecular variables such as the oestrogen and progesterone receptors (ER and PR, respectively), pS2 and Cathepsin D (CD). Using 260 fmol/mg protein as a cut-off point, 18% of the tumors presented as overexpressing p185. The p185 showed no relationship with any of the clinico-pathological variables studied except that its concentration was elevated in ductal and lobular histology types and in the moderate and poorly differentiated histology grades. With a median follow-up of 50 months (range 1-90), the univariate analysis of disease-free survival (DFS) and overall survival (OS) showed that the histology grade, tumor size, the number of infiltrated nodes, the p185 and the ER were the variables associated with the clinical course of the disease in the patients. In the multivariate analysis, however, only the tumor size, number of affected ganglia, the p 185 and the ER remained associated with the clinical progression of the disease. The patients with p185 overexpression had a risk, not only of relapse but also death from the disease, of more than twice that of the patients who had normal p185 concentrations. When the p 185 was divided into 3 categories based on +/-1 x SD above or below the mean, the patients with high and low p 185 showed, in the univariate analysis, a similar relationship with DFS but not with OS. In the multivariate analysis, both with the DFS as with the OS, only a high p 185 concentration retained its association with the clinical course of the disease in the patients. Our results suggest that by quantitatively determining (using ELISA) the p 185 oncoprotein, groups of cancer patients of high risk could be better identified for more effective clinical management. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:539 / 544
页数:6
相关论文
共 52 条
[1]   ASSOCIATION OF C-ERBB-2 EXPRESSION AND S-PHASE FRACTION IN THE PROGNOSIS OF NODE POSITIVE BREAST-CANCER [J].
ANBAZHAGAN, R ;
GELBER, RD ;
BETTELHEIM, R ;
GOLDHIRSCH, A ;
GUSTERSON, BA .
ANNALS OF ONCOLOGY, 1991, 2 (01) :47-53
[2]  
BORG A, 1990, CANCER RES, V50, P4332
[3]  
CARNEY W P, 1991, Journal of Tumor Marker Oncology, V6, P53
[4]  
CARTER CL, 1989, CANCER-AM CANCER SOC, V63, P181, DOI 10.1002/1097-0142(19890101)63:1<181::AID-CNCR2820630129>3.0.CO
[5]  
2-H
[6]   CORRELATION OF HER-2/NEU AMPLIFICATION WITH EXPRESSION AND WITH OTHER PROGNOSTIC FACTORS IN 1103 BREAST CANCERS [J].
CIOCCA, DR ;
FUJIMURA, FK ;
TANDON, AK ;
CLARK, GM ;
MARK, C ;
LEECHEN, GJ ;
POUNDS, GW ;
VENDELY, P ;
OWENS, MA ;
PANDIAN, MR ;
MCGUIRE, WL .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (16) :1279-1282
[7]  
CLARK GM, 1991, CANCER RES, V51, P944
[8]   C-ERBB-2 AND RAS EXPRESSION LEVELS IN BREAST-CANCER ARE CORRELATED AND SHOW A COOPERATIVE ASSOCIATION WITH UNFAVORABLE CLINICAL OUTCOME [J].
DATI, C ;
MURACA, R ;
TAZARTES, O ;
ANTONIOTTI, S ;
PERROTEAU, I ;
GIAI, M ;
CORTESE, P ;
SISMONDI, P ;
SAGLIO, G ;
DEBORTOLI, M .
INTERNATIONAL JOURNAL OF CANCER, 1991, 47 (06) :833-838
[9]  
Dittadi R, 1997, ANTICANCER RES, V17, P1245
[10]  
Eissa S, 1997, ANTICANCER RES, V17, P3091