|
|
||||||||
Articles |
A number of potent and selective non-steroidal aromatase inhibitors are now available for treatment of advanced breast cancer in postmenopausal women, of which anastrozole and letrozole, in particular, represent a significant advantage over the earlier agents in terms of both efficacy and tolerability. These agents are rapidly becoming established as the second-line therapy of choice in postmenopausal women with advanced disease, progressing on tamoxifen, and data on their efficacy as first-line treatment compared with tamoxifen will be available in the near future. Exemestane, a new, steroidal aromatase inhibitor which potentially lacks cross-resistance with non-steroidal agents is still in clinical development. The full potential of the new-generation aromatase inhibitors in the treatment of breast cancer is currently being investigated in a large program of clinical trials evaluating their use as adjuvant treatment following surgery in postmenopausal patients with early disease.
This article has been cited by other articles:
![]() |
J. Karnon, S. R. D. Johnston, T. Jones, and A. Glendenning A trial-based cost-effectiveness analysis of letrozole followed by tamoxifen versus tamoxifen followed by letrozole for postmenopausal advanced breast cancer Ann. Onc., November 1, 2003; 14(11): 1629 - 1633. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Paridaens, L. Dirix, C. Lohrisch, L. Beex, M. Nooij, D. Cameron, L. Biganzoli, T. Cufer, L. Duchateau, A. Hamilton, et al. Mature results of a randomized phase II multicenter study of exemestane versus tamoxifen as first-line hormone therapy for postmenopausal women with metastatic breast cancer Ann. Onc., September 1, 2003; 14(9): 1391 - 1398. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Buzdar and A. Howell Advances in Aromatase Inhibition: Clinical Efficacy and Tolerability in the Treatment of Breast Cancer Clin. Cancer Res., September 1, 2001; 7(9): 2620 - 2635. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |