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Journal of Clinical Oncology, Vol 21, Issue 6 (March), 2003: 984-990
© 2003 American Society for Clinical Oncology

Randomized Trial of Tamoxifen Versus Tamoxifen Plus Aminoglutethimide as Adjuvant Treatment in Postmenopausal Breast Cancer Patients With Hormone Receptor-Positive Disease: Austrian Breast and Colorectal Cancer Study Group Trial 6

Marianne Schmid, Raimund Jakesz, Hellmut Samonigg, Ernst Kubista, Michael Gnant, Christian Menzel, Michael Seifert, Karin Haider, Susanne Taucher, Brigitte Mlineritsch, Peter Steindorfer, Werner Kwasny, Michael Stierer, Christoph Tausch, Michael Fridrik, Viktor Wette, Günther Steger, Hubert Hausmaninger

From the Medical Department, Graz University, and Second Department of Surgery, Graz Hospital, Graz; Department of Surgery, Department of Gynecology, and First Medical Department, Vienna University, and Department of Surgery, Hanusch Medical Center, Vienna; Department of Special Gynecology and Third Medical Department, Salzburg Hospital, Salzburg; Department of Surgery, Wiener Neustadt Hospital, Wiener Neustadt; Department of Surgery, BHS Hospital Linz, and First Medical Department, Linz Hospital, Linz; and Department of Surgery, Sankt Veit Hospital, Sankt Veit, Austria.

Address reprint requests to Marianne Schmid, MD, Medical Department, Graz University, Auenbruggerplatz 15, Graz A-8036, Austria; email: marianne.schmid{at}kfunigraz.ac.at.

Purpose: To determine whether the addition of aminoglutethimide to tamoxifen is able to improve the outcome in postmenopausal patients with hormone receptor–positive, early-stage breast cancer.

Patients and Methods: A total of 2,021 postmenopausal women were randomly assigned to receive either tamoxifen for 5 years alone or tamoxifen in combination with aminoglutethimide (500 mg/d) for the first 2 years of treatment. Tamoxifen was administered at 40 mg/d for the first 2 years and at 20 mg/d for 3 years.

Results: All randomized and eligible patients were included in the analysis according to the intention-to-treat principle. After a median follow-up of 5.3 years, the 5-year disease-free survival in the aminoglutethimide plus tamoxifen group was 83.6% versus 83.7% in the monotherapy group (P = .89). The corresponding data for overall survival at 5 years were 91.4% and 91.2%, respectively (P = .74). More patients failed to complete combination treatment (13.7%) because of side effects as compared to tamoxifen alone (5.2%; P = .0001).

Conclusion: Aminoglutethimide given for 2 years in addition to tamoxifen for 5 years does not improve the prognosis of postmenopausal patients with receptor-positive, lymph node-negative or lymph node-positive breast cancer.


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