Letrozole, or CGS 20267, is an oral non-steroidal type II aromatase inhibitor first described in the literature in 1990. It is a third generation aromatase inhibitor like exemestane and anastrozole, meaning it does not significantly affect cortisol, aldosterone, and thyroxine.
Letrozole was granted FDA approval on 25 July 1997.
Letrozole is indicated to treat postmenopausal women with hormone receptor (HR) positive early breast cancer, postmenopausal women with early breast cancer who have periviously been treated with tamoxifen, and postmenopausal women with HR+ or unknown advanced breast cancer. Letrozole, given with ribociclib, is indicated to treat pre, peri, and postmenopausal women with HR+ and human epidermal growth factor 2 (HER2) negative advanced or metastatic breast cancer.
Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington, United States
University Hospital Mainz, Mainz, Germany
Froedtert Hospital, Milwaukee, Wisconsin, United States
Mayo Clinic in Florida, Jacksonville, Florida, United States
Mayo Clinic in Arizona, Scottsdale, Arizona, United States
Mayo Clinic in Rochester, Rochester, Minnesota, United States
Hospital Georges Pompidou, Paris, France
Istituto Europeo di Oncologia, Milan, Italy
Hospital Senhora da Oliveira, Guimarães, Portugal
Assiut Faculty of Medicine, Assiut, Egypt
UCLA / Jonsson Comprehensive Cancer Center, Los Angeles, California, United States
University of California Los Angeles, Santa Monica, California, United States
University of Miami, Miami, Florida, United States
University of Minnesota, Minneapolis, Minnesota, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.