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Research Article

Effects of exemestane and tamoxifen on hormone levels within the Tamoxifen Exemestane Adjuvant Multicentre (TEAM) Trial: results of a German substudy

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Pages 460-466 | Received 24 Jun 2011, Accepted 09 Nov 2011, Published online: 09 Feb 2012
 

ABSTRACT

Aim The aim of this study was to compare the effects of exemestane and tamoxifen on hormone levels in postmenopausal patients with hormone receptor-positive breast cancer within a Germany substudy of the Tamoxifen Exemestane Adjuvant Multinational (TEAM) trial.

Methods Within the TEAM trial, patients were randomized to receive adjuvant treatment with exemestane for 5 years or tamoxifen for 2.5–3 years followed by exemestane for 2–2.5 years. Serum levels of testosterone, dehydroepiandrosterone sulfate (DHEAS), sex hormone binding globulin (SHBG), follicle stimulating hormone (FSH) and parathyroid hormone (PTH)-intact were measured at screening and after 3, 6 and 12 months of treatment.

Results Data on hormone levels were available from 63 patients in the tamoxifen arm and 68 patients in the exemestane arm. Treatment with exemestane resulted in decreases from baseline in SHBG and PTH-intact levels, and increases from baseline in testosterone, DHEAS and FSH levels. Tamoxifen treatment resulted in increases from baseline in SHBG and PTH-intact, whereas levels of testosterone and FSH decreased and DHEAS levels did not change. At all time points assessed, the absolute change from baseline was significantly different between tamoxifen and exemestane for testosterone, SHBG, FSH and PTH-intact (all p < 0.0001).

Conclusions Exemestane and tamoxifen had statistically significantly different effects on hormone levels, including testosterone, SHBG, FSH and PTH-intact.

Conflict of interest Peyman Hadji has received an institutional grant and meeting travel reimbursement from Pfizer; Johanna Tams has received remuneration for statistical consultancy for Roche and review activities for Iomedico AG sponsored by Pfizer; Annette Hasenberg has received institutional funding, meeting travel reimbursement and remuneration for steering committee work from Pfizer, and speaker payments from Pfizer, GlaxoSmithKline, Sanofi Pasteur, Astra Zeneca, Medconcept. Dirk Kieback has received remuneration for board membership, grants and speaker payments from Pfizer and payment for developing educational materials from TRU Oncology. Thomas Bauer and Annette Kauka have no conflicts of interest.

Source of funding Medical writing assistance was provided by Caroline Masterman at Acumed (Tytherington, UK) and was funded by Pfizer, Inc.

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