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Previous Volume 361:766-776 August 20, 2009 Number 8 Next

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ABSTRACT

Background The aromatase inhibitor letrozole, as compared with tamoxifen, improves disease-free survival among postmenopausal women with receptor-positive early breast cancer. It is unknown whether sequential treatment with tamoxifen and letrozole is superior to letrozole therapy alone.

Methods In this randomized, phase 3, double-blind trial of the treatment of hormone-receptor–positive breast cancer in postmenopausal women, we randomly assigned women to receive 5 years of tamoxifen monotherapy, 5 years of letrozole monotherapy, or 2 years of treatment with one agent followed by 3 years of treatment with the other. We compared the sequential treatments with letrozole monotherapy among 6182 women and also report a protocol-specified updated analysis of letrozole versus tamoxifen monotherapy in 4922 women.

Results At a median follow-up of 71 months after randomization, disease-free survival was not significantly improved with either sequential treatment as compared with letrozole alone (hazard ratio for tamoxifen followed by letrozole, 1.05; 99% confidence interval [CI], 0.84 to 1.32; hazard ratio for letrozole followed by tamoxifen, 0.96; 99% CI, 0.76 to 1.21). There were more early relapses among women who were assigned to tamoxifen followed by letrozole than among those who were assigned to letrozole alone. The updated analysis of monotherapy showed that there was a nonsignificant difference in overall survival between women assigned to treatment with letrozole and those assigned to treatment with tamoxifen (hazard ratio for letrozole, 0.87; 95% CI, 0.75 to 1.02; P=0.08). The rate of adverse events was as expected on the basis of previous reports of letrozole and tamoxifen therapy.

Conclusions Among postmenopausal women with endocrine-responsive breast cancer, sequential treatment with letrozole and tamoxifen, as compared with letrozole monotherapy, did not improve disease-free survival. The difference in overall survival with letrozole monotherapy and tamoxifen monotherapy was not statistically significant. (ClinicalTrials.gov number, NCT00004205 [ClinicalTrials.gov] .)

Source Information

The members of the writing committee (Henning Mouridsen, M.D., chair, Anita Giobbie-Hurder, M.S., Aron Goldhirsch, M.D., Beat Thürlimann, M.D., Robert Paridaens, M.D., Ian Smith, M.D., Louis Mauriac, M.D., John F. Forbes, F.R.A.C.S., M.S., Karen N. Price, B.S., Meredith M. Regan, Sc.D., Richard D. Gelber, Ph.D., and Alan S. Coates, M.D.) assume full responsibility for the overall content and integrity of the article. The affiliations of the members of the writing committee are listed in the Appendix.

Address reprint requests to the International Breast Cancer Study Group (IBCSG) Coordinating Center, Effingerstr. 40, 3008 Bern, Switzerland, or at ibcsg18_BIG1-98{at}fstrf.org.

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