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Brief Title: Comparison Trial of Letrozole to Anastrozole in the Adjuvant Treatment of Postmenopausal Women With Hormone Receptor and Node Positive Breast Cancer
Official Title: Comparison Trial of Letrozole to Anastrozole in the Adjuvant Treatment of Postmenopausal Women With Hormone Receptor and Node Positive Breast Cancer
Study ID: NCT00248170
Brief Summary: Eligible patients will be post-menopausal hormone receptor- and lymph node-positive females who recently underwent primary surgery for breast cancer. Patients will be randomized to letrozole (2.5 mg per day for 5 years) vs anastrozole (1 mg per day for 5 years). Follow up will occur for 5 years after the completion of enrollment for survival and disease status updates.
Detailed Description:
Minimum Age: 33 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
Birmingham Hematology and Oncology Associates, Birmingham, Alabama, United States
Comprehensive Cancer Institute, Huntsville, Alabama, United States
Northern Arizona Hematology/Oncology Associates, P.C., Flagstaff, Arizona, United States
Oncology & Hematology Associates, PC, New London, Connecticut, United States
Florida Cancer Specialists, Fort Meyers, Florida, United States
Sarah Cannon Research Institute, Jacksonville, Florida, United States
Cancer Centers of Florida PA, Ocoee, Florida, United States
Florida Cancer Institute, Orlando, Florida, United States
Gulfcoast Oncology Associates, St. Petersburg, Florida, United States
University Cancer & Blood Center, LLC, Athens, Georgia, United States
Central Indiana Cancer Centers, Indianapolis, Indiana, United States
Kansas City Cancer Center, Overland Park, Kansas, United States
Wichita Community Clinical Oncology Program, Wichita, Kansas, United States
Center for Cancer & Blood Disorders, Bethesda, Maryland, United States
St. Louis Cancer & Breast Institute, St. Louis, Missouri, United States
New York Oncology Hematology, P.C. NYOH Latham, Troy, New York, United States
Raleigh Hematology Oncology Associates, Cary, North Carolina, United States
Aultman Cancer Center, Canton, Ohio, United States
Sarah Cannon Oncology Hematology Care, Inc, Cincinnati, Ohio, United States
Oncology Associates of Oregon, PC, Eugene, Oregon, United States
Medical Oncology Associates of Wyorning Valley, PC, Kingston, Pennsylvania, United States
Chattanooga Oncology and Hematology Assoicates, PC, Chattanooga, Tennessee, United States
Sarah Cannon Research Institute, Nashville, Tennessee, United States
Texas Oncology, P.A., Bedford, Texas, United States
Center for Oncology Research and Treatment, PA, Dallas, Texas, United States
Texas Cancer Center ( Medical City Dallas Hospital), Dallas, Texas, United States
Texas Oncology Presbyterian Hospital, Dallas, Texas, United States
Texas Oncology Sammons Cancer Center, Dallas, Texas, United States
Texas Oncology Texas Oncology PA, Dallas, Texas, United States
Texas Cancer Center Denton, Denton, Texas, United States
El Paso Cancer Treatment Ctr-East, El Paso, Texas, United States
Texas Oncology, P.A., Fort Worth, Texas, United States
San Antonio Tumor and Blood Clinic, Fredericksburg, Texas, United States
MD Anderson Cancer Center/University of Texas, Houston, Texas, United States
Longview Cancer Center, Longview, Texas, United States
South Texas Cancer Center- McAllen, McAllen, Texas, United States
Allison Cancer Center, Midland, Texas, United States
Texas Cancer Center- Sherman, Sherman, Texas, United States
Tyler Cancer Center, Tyler, Texas, United States
Waco Cancer and Research Center, Waco, Texas, United States
Virginia Cancer Specialists, PC, Fairfax, Virginia, United States
Northwest Cancer Specialists, P.C., Vancover, Washington, United States
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Name: Novartis Pharmaceuticals
Affiliation: Novartis Pharmaceuticals
Role: STUDY_DIRECTOR