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  3. Exemestane Versus Anastrozole in Postmenopausal Women With Early Breast Cancer: NCIC CTG MA.27—A Randomized Controlled Phase III Trial

Exemestane Versus Anastrozole in Postmenopausal Women With Early Breast Cancer: NCIC CTG MA.27—A Randomized Controlled Phase III Trial

Details
Publisher DOI
10.1200/JCO.2012.44.7805
PubMed ID
23358971
Abstract
PURPOSE

In patients with hormone-dependent postmenopausal breast cancer, standard adjuvant therapy involves 5 years of the nonsteroidal aromatase inhibitors anastrozole and letrozole. The steroidal inhibitor exemestane is partially non-cross-resistant with nonsteroidal aromatase inhibitors and is a mild androgen and could prove superior to anastrozole regarding efficacy and toxicity, specifically with less bone loss.

PATIENTS AND METHODS

We designed an open-label, randomized, phase III trial of 5 years of exemestane versus anastrozole with a two-sided test of superiority to detect a 2.4% improvement with exemestane in 5-year event-free survival (EFS). Secondary objectives included assessment of overall survival, distant disease-free survival, incidence of contralateral new primary breast cancer, and safety.

RESULTS

In the study, 7,576 women (median age, 64.1 years) were enrolled. At median follow-up of 4.1 years, 4-year EFS was 91% for exemestane and 91.2% for anastrozole (stratified hazard ratio, 1.02; 95% CI, 0.87 to 1.18; P = .85). Overall, distant disease-free survival and disease-specific survival were also similar. In all, 31.6% of patients discontinued treatment as a result of adverse effects, concomitant disease, or study refusal. Osteoporosis/osteopenia, hypertriglyceridemia, vaginal bleeding, and hypercholesterolemia were less frequent on exemestane, whereas mild liver function abnormalities and rare episodes of atrial fibrillation were less frequent on anastrozole. Vasomotor and musculoskeletal symptoms were similar between arms.

CONCLUSION

This first comparison of steroidal and nonsteroidal classes of aromatase inhibitors showed neither to be superior in terms of breast cancer outcomes as 5-year initial adjuvant therapy for postmenopausal breast cancer by two-way test. Less toxicity on bone is compatible with one hypothesis behind MA.27 but requires confirmation. Exemestane should be considered another option as up-front adjuvant therapy for postmenopausal hormone receptor-positive breast cancer.
Date Issued
2013-04-10
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Language(s)
en
Author(s)
Goss, Paul E.
Ingle, James N.
Pritchard, Kathleen I.
Ellis, Matthew J.
Sledge, George W.
Budd, G. Thomas
Rabaglio, Manuela Elena  
Universitätsklinik für Medizinische Onkologie  
Ansari, Rafat H.
Johnson, David B.
Tozer, Richard
D'Souza, David P.
Chalchal, Haji
Spadafora, Silvana
Stearns, Vered
Perez, Edith A.
Liedke, Pedro E. R.
Lang, Istvan
Elliott, Catherine
Gelmon, Karen A.
Chapman, Judy-Anne W.
Shepherd, Lois E.
Additional Credits
Universitätsklinik für Medizinische Onkologie  
Journal
Journal of clinical oncology
Publisher
American Society of Clinical Oncology
ISSN
0732-183X
Access(Rights)
metadata.only
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