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PMID: 2569032 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

HER-2/neu oncogene protein and prognosis in breast cancer.

Tandon AK, Clark GM, Chamness GC, Ullrich A, McGuire WL

Abstract

Amplification of the HER-2/neu oncogene was recently reported to predict poor clinical outcome in node-positive breast cancer patients. Since expression of the oncogene as its protein product might be even more closely related than gene amplification to disease progression, we have now examined levels of the HER-2/neu oncogene protein for its prognostic potential in both node-positive and node-negative breast cancer. Using Western blot analysis, levels of this protein were determined in 728 primary human breast tumor specimens. We examined relationships between this protein and other established markers of prognosis, as well as clinical outcome. In node-negative patients (n = 378), the HER-2/neu protein failed to predict disease outcome. However, in node-positive patients (n = 350), those patients with higher HER-2/neu protein had statistically shorter disease-free (P = .0014) and overall survival (P less than .0001) than patients with lower levels of the protein. Higher HER-2/neu protein was found in tumors without estrogen receptor (ER) (P = .02) or progesterone receptor (PgR) (P = .0003), and in patients with more than three positive lymph nodes (P = .04). A significant correlation between levels of the HER-2/neu gene protein and amplification of the gene itself was also found (n = 48, P less than .001). Multivariate analyses in these patients showed that the HER-2/neu protein is a significant independent predictor of both the disease-free and the overall survival in node-positive breast cancer, even when other prognostic factors are considered.

MeSH Terms
Antibody Specificity Biomarkers, Tumor/analysis Blotting, Western Breast Neoplasms/analysis,genetics Cell Line Electrophoresis, Polyacrylamide Gel Female Gene Amplification Humans Oncogene Proteins, Viral/analysis Probability Prognosis Protein Kinases/analysis Proto-Oncogenes Receptor, ErbB-2 Receptors, Estrogen/analysis Receptors, Progesterone/analysis
Chemicals
Biomarkers, Tumor Oncogene Proteins, Viral Receptors, Estrogen Receptors, Progesterone Protein Kinases Receptor, ErbB-2
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Tandon A K
Department of Medicine, University of Texas Health Science Center, San Antonio, 78284-7884.
Clark G M
Chamness G C
Ullrich A
McGuire W L
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
0732-183X
Published
1989-08-00
Pages
1120-8
Language
English
Region
United States
NLM ID
8309333
Subset
IM
Grants
NCI NIH HHS · CA 30195 · United States
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