Aromatase Inhibitors in Breast Cancer
Until recently, tamoxifen, a nonsteroidal antiestrogen, was the mainstay of endocrine treatment of breast cancer. However, new aromatase inhibitors that are many times more potent and specific than the first such agent, aminoglutethimide, are changing the management of breast cancer in postmenopausa...
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Published in | The New England journal of medicine Vol. 348; no. 24; pp. 2431 - 2442 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Boston, MA
Massachusetts Medical Society
12.06.2003
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Subjects | |
Online Access | Get full text |
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Summary: | Until recently, tamoxifen, a nonsteroidal antiestrogen, was the mainstay of endocrine treatment of breast cancer. However, new aromatase inhibitors that are many times more potent and specific than the first such agent, aminoglutethimide, are changing the management of breast cancer in postmenopausal women. This review discusses the role of aromatase inhibitors such as letrozole, anastrozole, and exemestane in the treatment of breast cancer.
The third-generation aromatase inhibitors provide novel approaches to the endocrine treatment of breast cancer. These drugs are effectively challenging tamoxifen, the previous gold standard of care,
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for use in postmenopausal patients with estrogen-receptor–positive cancers, who make up the majority of patients with breast cancer. These agents are also being considered for use in chemoprevention, a strategy in which tamoxifen has already been shown to reduce the incidence of breast cancer.
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In this article, we review the current role of aromatase inhibitors and assess their potential for clinical use. Other reviews that may be of interest to specialists are . . . |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 0028-4793 1533-4406 |
DOI: | 10.1056/NEJMra023246 |