Randomized Trial of Letrozole Following Tamoxifen as Extended Adjuvant Therapy in Receptor-Positive Breast Cancer: Updated Findings from NCIC CTG MA.17

Background: Most recurrences in women with breast cancer receiving 5 years of adjuvant tamoxifen occur after 5 years. The MA.17 trial, which was designed to determine whether extended adjuvant therapy with the aromatase inhibitor letrozole after tamoxifen reduces the risk of such late recurrences, w...

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Veröffentlicht in:JNCI : Journal of the National Cancer Institute 2005-09, Vol.97 (17), p.1262-1271
Hauptverfasser: Goss, Paul E., Ingle, James N., Martino, Silvana, Robert, Nicholas J., Muss, Hyman B., Piccart, Martine J., Castiglione, Monica, Tu, Dongsheng, Shepherd, Lois E., Pritchard, Kathleen I., Livingston, Robert B., Davidson, Nancy E., Norton, Larry, Perez, Edith A., Abrams, Jeffrey S., Cameron, David A., Palmer, Michael J., Pater, Joseph L.
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Sprache:eng
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Zusammenfassung:Background: Most recurrences in women with breast cancer receiving 5 years of adjuvant tamoxifen occur after 5 years. The MA.17 trial, which was designed to determine whether extended adjuvant therapy with the aromatase inhibitor letrozole after tamoxifen reduces the risk of such late recurrences, was stopped early after an interim analysis showed that letrozole improved disease-free survival. This report presents updated findings from the trial. Methods: Postmenopausal women completing 5 years of tamoxifen treatment were randomly assigned to a planned 5 years of letrozole (n = 2593) or placebo (n = 2594). The primary endpoint was disease-free survival (DFS); secondary endpoints included distant disease-free survival, overall survival, incidence of contralateral tumors, and toxic effects. Survival was examined using Kaplan–Meier analysis and log-rank tests. Planned subgroup analyses included those by axillary lymph node status. All statistical tests were two-sided. Results: After a median follow-up of 30 months (range = 1.5–61.4 months), women in the letrozole arm had statistically significantly better DFS and distant DFS than women in the placebo arm (DFS: hazard ratio [HR] for recurrence or contralateral breast cancer = 0.58, 95% confidence interval [CI] = 0.45 to 0.76; P
ISSN:0027-8874
1460-2105
DOI:10.1093/jnci/dji250