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Ther Clin Risk Manag. 2008 December; 4(6): 1295–1304.
Published online 2008 December.
PMCID: PMC2643110
Exemestane in early breast cancer: a review
Michael Untch1 and Christian Jackisch2
1Interdisciplinary Breast Centre, Helios Klinikum Berlin-Buch, University Charité, Berlin, Germany;
2Department of Gynecology/Obstetrics, Klinikum Offenbach GmbH, Offenbach, Germany
Correspondence: Prof Dr med. Michael Untch, Head of Department of Gynecology/Gynecologic Oncology, Head of the Interdisciplinary Breast Center, Helios Klinikum Berlin-Buch, Academic Hospital of the University Charité, Schwanebecker Chaussee 50, 13125 Berlin, Germany, Tel +49 030 9401/53300, Fax +49 030 9401/53309, Email muntch/at/berlin.helios-kliniken.de
Abstract
The adjuvant treatment of women with endocrine-sensitive early breast cancer has been dominated for the last 40 years by tamoxifen. However, the side-effects associated with this therapy have prompted a search for safer and biochemically more selective endocrine agents and led to the development of the third-generation aromatase inhibitors (AIs) anastrozole, letrozole and exemestane. Promising results in advanced disease have paved the way for treating early breast cancer, and AIs are increasingly replacing tamoxifen in the adjuvant setting. Several large, randomized trials with AIs have been completed or are ongoing in women with early-stage breast cancer, documenting the significant impact that these drugs are making on the risk for recurrence of breast cancer. As a result, there is increasing and widespread use of AI therapy for the treatment of early-stage endocrine-responsive breast cancer. This review summarizes the data for exemestane in the adjuvant setting, showing that a switch to exemestane after 2 to 3 years of tamoxifen therapy is associated with a statistically significant survival benefit and is regarded as being sensitive by international and national experts.
Keywords: early breast cancer, adjuvant setting, endocrine-sensitive, tamoxifen, aromatase inhibitor, exemestane, switch, IES 31, NSABP B-33, TEAM