For postmenopausal women with endocrine-responsive early breast cancer, letrozole monotherapy provides a greater reduction in breast cancer recurrence and mortality than tamoxifen monotherapy, according to a new study.
After a median of eight years of follow-up from a large, randomized trial, women who had received five years of treatment with letrozole, an aromatase inhibitor, were less likely to die or have their cancer recur during follow-up than women who had five years of treatment with tamoxifen. In addition, five years of sequential treatment—either two years of letrozole followed by three years of tamoxifen or two years of tamoxifen followed by three years of letrozole—did not produce better results than five years of letrozole alone.
The study followed 8,010 postmenopausal women with invasive breast cancer that had been removed surgically. Women who received letrozole alone had a disease-free survival rate of 73.7% at eight years compared with a rate of 70.4% for women who received tamoxifen alone. Women who receive letrozole alone also had better overall survival at eight years than women receiving tamoxifen alone (83.4% versus 81.2%).
According to the authors, the two drugs have different side effects, and this study shows that women have options. If the side effects from letrozole are intolerable, benefits are maintained by switching to tamoxifen rather than stopping hormonal therapy altogether. Novartis, the manufacturer of letrozole, provided funding for the trial, along with the National Cancer Institute and the International Breast Cancer Study Group.
- Regan, M.M., Neven, P., Gioggie-Hurder, A., Goldhirsch, A., Ejlertsen, B. Mauriac, L., . . . Thurlimann, B. (2011). Assessment of letrozole and tamoxifen alone and in sequence for postmenopausal women with steroid hormone receptor-positive breast cancer: The BIG 1–98 randomised clinical trial at 8·1 years median follow-up. Lancet Oncology, 12, 1101–1108. doi: 10.1016/S1470-2045(11)70270–4
Contributor Deborah McBride, RN, MSN, CPON®, is a staff nurse IV at the Kaiser Permanente Oakland Medical Center and an assistant professor at Samuel Merritt University in Oakland, CA.