Bookmark this pageiconPrint this pageE-mail this page

This is an international site for FEMARA® (letrozole) and is intended for Health Care Professionals outside the U.S. The information on the site is not country-specific, and may contain information that is outside the approved indications in the country in which you are located. Please contact your local Novartis representative for the latest information specific to your country.

Femara and Breast Cancer Information for International Healthcare Professionals Femara and Breast Cancer Information for US residents Femara and Breast Cancer Information for Patients Outside the US

MA-17 is the first study to prove the benefit of extended adjuvant therapy after adjuvant tamoxifen in postmenopausal women with HR+ early breast cancer1,2

Design of MA-17 trial in postmenopausal women with HR+ early breast cancer2

Femara | Design of MA-17 trial in postmenopausal women with HR+ early breast cancer

MA-17 was a double-blind, randomized, placebo-controlled trial conducted in more than 5100 postmenopausal women with hormone receptor positive or receptor-unknown primary breast cancer who were disease free after adjuvant tamoxifen.1

End points included1,2:


A significant disease-free survival benefit led to unblinding approximately 1 year early (median time to follow-up: 2.4 years).2

An extension of MA-17

MA-17 investigators announced a planned rerandomization and follow-up of the FEMARA® (letrozole) arm for an additional 5 years to assess the long-term efficacy and safety of FEMARA® as well as to determine the optimal duration of FEMARA® (letrozole) treatment.3

Prescribe the only therapy that has been studied and approved for use in the extended adjuvant setting following 5 years of tamoxifen: FEMARA® (letrozole).1,4,5

See results from the MA-17 trial

To read about significant benefits with FEMARA® in the initial adjuvant setting, click here.

Extended adjuvant treatment of hormone-dependent early breast cancer in postmenopausal women who have received prior standard adjuvant tamoxifen therapy for 5 years.

References: 1. FEMARA® (letrozole) [summary of product characteristics]. Basel, Switzerland: Novartis Pharma AG; 2009. 2. Goss PE, Ingle JN, Martino S, et al. Randomized trial of letrozole following tamoxifen as extended adjuvant therapy in receptor-positive breast cancer: updated findings from NCIC CTG MA.17. J Natl Cancer Inst. 2005;97:1262-1271.
3. Letrozole in breast cancer [correspondence]. N Engl J Med. 2004;350:727-730. 4. Arimidex® (anastrazole) [summary of product characteristics]. Luton, UK: AstraZeneca UK Limited; 2007. 5. Aromasin® (exemestane) [summary of product characteristics]. Sandwich, UK: Pharmacia Ltd; 2008.