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

被引:198
作者
Goss, Paul E. [1 ]
Ingle, James N. [2 ]
Pritchard, Kathleen I. [10 ,11 ]
Ellis, Matthew J. [3 ]
Sledge, George W. [4 ]
Budd, G. Thomas [6 ]
Rabaglio, Manuela [18 ,19 ]
Ansari, Rafat H. [5 ]
Johnson, David B. [7 ]
Tozer, Richard [12 ]
D'Souza, David P. [13 ]
Chalchal, Haji [16 ]
Spadafora, Silvana [14 ]
Stearns, Vered [8 ]
Perez, Edith A. [9 ]
Liedke, Pedro E. R. [1 ]
Lang, Istvan [20 ]
Elliott, Catherine [15 ]
Gelmon, Karen A. [17 ]
Chapman, Judy-Anne W. [15 ]
Shepherd, Lois E. [15 ]
机构
[1] Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Mayo Clin, Rochester, MN USA
[3] Washington Univ, Siteman Canc Ctr, St Louis, MO USA
[4] Indiana Univ Hlth, Indianapolis, IN USA
[5] Northern Indiana Canc Res Consortium, South Bend, IN USA
[6] Cleveland Clin, Cleveland, OH 44106 USA
[7] Canc Ctr Kansas, Wichita, KS USA
[8] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[9] Mayo Clin, Jacksonville, FL 32224 USA
[10] Sunnybrook Odette Canc Ctr, Toronto, ON, Canada
[11] Univ Toronto, Toronto, ON, Canada
[12] Juravinski Canc Ctr, Hamilton, ON, Canada
[13] London Reg Canc Program, London, England
[14] Algoma Reg Canc Ctr, Sault Ste Marie, ON, Canada
[15] NCIC Clin Trials Grp, Kingston, ON, Canada
[16] Regina Gen Hosp, Regina, SK, Canada
[17] British Columbia Canc Agcy, Vancouver, BC V5Z 4E6, Canada
[18] Int Breast Canc Study Grp Coordinating Ctr, Bern, Switzerland
[19] Univ Bern, Inselspital, CH-3010 Bern, Switzerland
[20] Natl Inst Oncol, Budapest, Hungary
基金
美国国家卫生研究院;
关键词
NONSTEROIDAL AROMATASE INHIBITORS; ADJUVANT ENDOCRINE THERAPY; ADHERENCE; TAMOXIFEN;
D O I
10.1200/JCO.2012.44.7805
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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. J Clin Oncol 31:1398-1404. (C) 2013 by American Society of Clinical Oncology
引用
收藏
页码:1398 / 1404
页数:7
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