Breast Cancer Research and Treatment

, Volume 137, Issue 2, pp 465–470 | Cite as

Adjuvant therapy with tamoxifen compared to aromatase inhibitors for 257 male breast cancer patients

  • Holm EggemannEmail author
  • Atanas Ignatov
  • Bobbie J. Smith
  • Udo Altmann
  • Gunter von Minckwitz
  • Freidrich W. Röhl
  • Mark Jahn
  • Serban-Dan Costa
Clinical trial


To determine the impact of adjuvant treatment with tamoxifen and aromatase inhibitors (AI) on the survival of men with breast cancer. We analyzed 257 male patients with hormone-receptor-positive breast cancer from numerous German population-based cancer registries treated with tamoxifen (N = 207) or aromatase inhibitors (N = 50). The median follow-up was 42.2 (range 2–115) months. Median age at diagnosis was 68 (range 36–91) years. Thirty-seven (17.9 %) patients treated with tamoxifen and 16 (32.0 %) patients treated with AI died (log rank p = 0.007). After the adjustment for the patient’s age, tumor size, node status, and tumor grading, the AI treatment was linked to a 1.5-fold increase in risk of mortality compared to tamoxifen (HR 1.55; 95 % CI: 1.13–2.13; p = 0.007). The overall survival in male breast cancer was significantly better after adjuvant treatment with tamoxifen compared to an aromatase inhibitor. Tamoxifen should be considered as the treatment of choice for hormone-receptor-positive male breast cancer.


Male breast cancer Tamoxifen Aromatase inhibitor Adjuvant treatment 

List of abbreviations


Aromatase inhibitors


Confidence interval


Ductal carcinoma in situ


Estrogen receptor human epidermal growth factor


Receptor 2


Hazard ratio


Male breast cancer




Overall survival


Progesterone receptor





We would like to thank Mathias Uhlig, PhD, Sabine Kleinefeld, and Christiane Praetor for their excellent work in project and data management.

We would also like to thank the following cancer registries for their cooperation, without which this study would not have been possible: Tumorzentrum Augsburg, Krebsregister in Klinikum Bayreuth GmbH, St. Gertrauden-Krankenhaus (Tumorzentrum gemeinnütziger und konfessioneller Krankenhäuser in Berlin (TZGKB)), Vivantes Tumorzentrum (Berlin), Tumorzentrums Chemnitz e.V., Tumorzentrum of the Staedische Klinikum in Dessau, Tumorzentrum Erfurt e.V., Tumorzentrum Ludwig Heilmeyer (Comprehensive Cancer Center Freiburg), Arbeitsgruppe zur Koordination Klinischer Krebsregister (AKKK) Giessen, Tumorzentrum Ostsachsen e. V. Goerlitz, Tumorzentrum Halle, Gynaekologisches Tumorzentrum am Diakonie-Klinikum Hamburg, Tumorzentrum Heilbronn-Franken, HELIOS Klinikum Berlin Buch, UniversitätsTumorCentrum Jena, Tumorzentrum Koblenz am Kemperhof, Tumorzentrum Land Brandenburg, Tumorzentrum Magdeburg/Sachsen-Anhalt e.V., Tumorzentrum Neubrandenburg, Tumorzentrum Südharz e.V. in Nordhausen, Krebsregister Rostock, Tumorzentrum Schwerin-Westmecklenburg, Tumorzentrum Suhl e. V., and the Tumorzentrum Zwickau e.V.

Conflict of interests

The authors declare no conflicts of interest.


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Copyright information

© Springer Science+Business Media New York 2012

Authors and Affiliations

  • Holm Eggemann
    • 1
    Email author
  • Atanas Ignatov
    • 1
  • Bobbie J. Smith
    • 2
  • Udo Altmann
    • 3
  • Gunter von Minckwitz
    • 4
  • Freidrich W. Röhl
    • 5
  • Mark Jahn
    • 6
  • Serban-Dan Costa
    • 1
  1. 1.University Women’s ClinicOtto-von-Guericke UniversityMagdeburgGermany
  2. 2.Hannover Medical SchoolHannoverGermany
  3. 3.Clinical Tumor Registry CoordinationJustus Liebig UniversityGiessenGermany
  4. 4.German Breast GroupNeu-IsenburgGermany
  5. 5.Institute of Biometrics and Medical InformaticsOtto-von-Guericke UniversityMagdeburgGermany
  6. 6.Helios Klinikum, Berlin BuchBerlinGermany

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