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Review
. 2011 May;8(5):307-11.
doi: 10.1038/nrclinonc.2010.185. Epub 2010 Dec 14.

HER2 and hormone receptor-positive breast cancer--blocking the right target

Affiliations
Review

HER2 and hormone receptor-positive breast cancer--blocking the right target

Javier Cortés et al. Nat Rev Clin Oncol. 2011 May.

Abstract

HER2-positive tumors have a worse prognosis than HER2-negative cancers. Although the standard treatment for HER2-positive metastatic breast cancer is chemotherapy and trastuzumab, the combination of aromatase inhibitors with anti-HER2 therapies has become an available strategy in patients with HER2-positive and hormone receptor-positive tumors. However, although this new treatment option is more effective than hormone therapy alone, it has not been compared with the standard chemotherapy and trastuzumab-based regimens. In fact, the activity observed in randomized clinical trials with chemotherapy and anti-HER2 therapies seems to be higher than that observed with aromatase inhibitors and trastuzumab-based or lapatinib-based therapies. In this article, we highlight the importance of considering chemotherapy and anti-HER2 therapy as the standard of care in HER2-positive and hormone receptor-positive tumors.

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References

    1. J Clin Oncol. 2009 Nov 20;27(33):5492-4 - PubMed
    1. Science. 1987 Jan 9;235(4785):177-82 - PubMed
    1. Proc Natl Acad Sci U S A. 2003 Sep 2;100(18):10393-8 - PubMed
    1. Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8418-23 - PubMed
    1. Nature. 2000 Aug 17;406(6797):747-52 - PubMed

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