Skip Navigation


Annals of Oncology Advance Access originally published online on July 17, 2008
Annals of Oncology 2008 19(11):1853-1859; doi:10.1093/annonc/mdn402
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplementary Data
Right arrow All Versions of this Article:
19/11/1853    most recent
mdn402v1
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Somlo, G.
Right arrow Articles by Danenberg, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Somlo, G.
Right arrow Articles by Danenberg, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2008. Published by Oxford University Press on behalf of the European Society for Medical Oncology. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

breast cancer

Molecular profiling including epidermal growth factor receptor and p21 expression in high-risk breast cancer patients as indicators of outcome

G. Somlo1,*, P. Chu2, P. Frankel4, W. Ye5, S. Groshen5, J. H. Doroshow1, K. Danenberg6 and P. Danenberg3

1 Department of Medical Oncology and Therapeutics Research
2 Department of Anatomic Pathology, City of Hope National Medical Center, Duarte, CA
3 Department of Biochemistry, Keck School of Medicine, University of Southern California, Los Angeles, CA
4 Department of Biostatistics, City of Hope National Medical Center, Duarte, CA
5 Department of Biostatistics, Keck School of Medicine, University of Southern California, Los Angeles, CA
6 Response Genetics, Inc., Los Angeles, CA, USA

* Correspondence to: Dr G. Somlo, Department of Medical Oncology, City of Hope National Medical Center, 1500 East Duarte Road, Duarte, CA 91010-3000, USA. Tel: +1 626 359-8111 ext. 62867; Fax: +1 626 301-8898; E-mail: gsomlo{at}coh.org.

Background: Patients with high-risk primary breast cancer remain at high risk for relapse. More precise prognostic and predictive tools are needed to improve treatment of such patients.

Patients and methods: Formalin-fixed, paraffin-embedded tumors from 239 high-risk breast cancer patients were examined for expression of human epidermal growth factor receptor 2 (HER2), epidermal growth factor receptor (EGFR), estrogen receptor, progesterone receptor, Ki-67, p16, p21, p27, and p53 by immunohistochemistry. Gene expression of EGFR, HER2, glutathione S-transferase-Pi (GSTP1), excision repair cross complementation1 (ERCC1), p21, β-tubulin-3, multidurg resistance (MDR1), cyclooxygenase2 (COX2), and cyclin-E was measured by RT-PCR.

Results: Eighty percent of patients presented with locally advanced, or ≥10 axillary nodal metastasis, and 20% with inflammatory breast cancer. The median age was 46 years (26–62 years) and the median number of involved axillary lymph nodes was 12 (0–42). At a median follow-up of 86 months, relapse-free survival (RFS) and overall survival for the entire group were 50% (95% CI 43% to 57%) and 62% (95% CI 56% to 69%). Multivariate Cox stepwise analysis resulted in a simple model for RFS consisting only of p21 expression, EGFR expression assessed by RT-PCR, and number of axillary nodal metastases.

Conclusion: A prognostic model on the basis of the expression of a limited number of proteins and genes may help to guide target-specific therapies in patients with high-risk breast cancer.

Key words: epidermal growth factor receptor, high-risk breast cancer, prognosis, p21

Received for publication May 8, 2008. Accepted for publication May 26, 2008.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Cancer Res.Home page
N. Seitzer, T. Mayr, S. Streit, and A. Ullrich
A Single Nucleotide Change in the Mouse Genome Accelerates Breast Cancer Progression
Cancer Res., January 15, 2010; 70(2): 802 - 812.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.