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Clinical Cancer Research 14, 8019, December 15, 2008. doi: 10.1158/1078-0432.CCR-08-0974
© 2008 American Association for Cancer Research

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CCR Focus

Emerging Biomarkers and New Understanding of Traditional Markers in Personalized Therapy for Breast Cancer

Mitch Dowsett1,2 and Anita K. Dunbier1,2

Authors' Affiliations: 1 Academic Department of Biochemistry, Royal Marsden Hospital and 2 The Breakthrough Breast Cancer Research Centre, The Institute of Cancer Research, London, United Kingdom

Requests for reprints: Anita K. Dunbier, Academic Department of Biochemistry, Royal Marsden Hospital, Fulham Road, London, SW36JJ, United Kingdom. Phone: 44-207-808-2883; Fax: 44-207-376-3918; E-mail: anita.dunbier{at}icr.ac.uk.

Abstract

The era of personalized medicine is likely to see an escalation in the use of biomarkers to ensure breast cancer patients receive optimal treatment. A combination of prognostic and predictive biomarkers should enable better quantification of the residual risk faced by patients and indicate the potential value of additional treatment. Established biomarkers such as estrogen receptor and progesterone receptor already play a significant role in the selection of patients for endocrine therapy. Human epidermal growth factor receptor 2 (HER2) is recognized as a strong predictor of response to trastuzumab whereas, more recently, the role of estrogen receptor and HER2 as negative and positive indicators for chemotherapy has also been explored. Ki67 has traditionally been recognized as a modest prognostic factor, but recent neoadjuvant studies suggest that on-treatment measurement may be a more effective predictor of treatment efficacy for both endocrine treatment and chemotherapy. The last decade has seen the emergence of numerous multigene expression profiles that aim to outdo traditional predictive and prognostic factors. The Oncotype DX assay and the MammaPrint profile are currently undergoing prospective clinical trials to clearly define their role. Other gene expression–based assays also show potential but are yet to be tested clinically. Rigorous comparison of these emerging markers with current treatment selection criteria will be required to determine whether they offer significant benefit to justify their use.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2008 by the American Association for Cancer Research.