Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/42586
Title: 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
Authors: Bohn, Uriel
Aguiar, José
Bilbao Sieyro, Cristina 
Murias, Adolfo
Vega, Victor
Chirino Godoy, Ricardo 
Díaz-Chico, Nicolas
Díaz Chico, Juan Carlos 
UNESCO Clasification: 320101 Oncología
Keywords: Breast cancer
p185 oncoprotein
ELISA
Her-2 Neu Oncogene
C-Erbb-2 Expression, et al
Issue Date: 2002
Publisher: 0020-7136
Journal: International Journal of Cancer 
Abstract: Our study attempts to determine the prognostic value of the quantitative measurement of the oncoprotein p185Her‐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 clinico‐pathological 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 p185 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 p185 was divided into 3 categories based on ±1 × SD above or below the mean, the patients with high and low p185 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 p185 concentration retained its association with the clinical course of the disease in the patients. Our results suggest that by quantitatively determining (using ELISA) the p185 oncoprotein, groups of cancer patients of high risk could be better identified for more effective clinical management.
URI: http://hdl.handle.net/10553/42586
ISSN: 0020-7136
DOI: 10.1002/ijc.10612
Source: International Journal Of Cancer [ISSN 0020-7136],v. 101 (6), p. 539-544
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