Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Jun;23(3):201-8.
doi: 10.1016/j.breast.2014.01.016. Epub 2014 Mar 1.

The therapeutic role of fulvestrant in the management of patients with hormone receptor-positive breast cancer

Affiliations
Review

The therapeutic role of fulvestrant in the management of patients with hormone receptor-positive breast cancer

Eva Ciruelos et al. Breast. 2014 Jun.

Abstract

Although selective estrogen receptor modulators (SERMs), such as tamoxifen, or aromatase inhibitors (AIs), such as anastrozole, are the preferred endocrine treatment approach for most patients with hormone receptor-positive breast cancer, many patients progress despite this therapy or become resistant. Fulvestrant is a selective estrogen receptor down-regulator (SERD) that has demonstrated activity and efficacy in patients with hormone receptor-positive breast cancer previously untreated or treated with hormonal therapy. The efficacy of fulvestrant has been demonstrated in the neoadjuvant and metastatic settings, either alone or in combination with other therapies such as anastrozole or targeted drugs. Additionally, 500 mg of fulvestrant have been shown to be more effective than 250 mg, without significant differences in the toxicity profile. In this review, the unique mode of action of fulvestrant and the clinical data for different dosing regimens both alone or in combination with other drugs is critically assessed.

Keywords: Aromatase inhibitor; Endocrine treatment; Fulvestrant; Hormone receptor-positive breast cancer; Selective estrogen receptor down-regulators; Selective estrogen receptor modulators.

PubMed Disclaimer

Publication types

MeSH terms

LinkOut - more resources