The purpose of this study is to assess Efficacy and Safety of Extended Adjuvant Treatment With Letrozole in Postmenopausal Women With Hormone Receptor Positive Breast Cancer Who Complete 5 Years of Toremifene
1. Primary purpose To evaluate disease free survival rate (DFS) after taking 36 months with Letrozole in postmenopausal women with hormone receptor positive breast cancer who complete 5 years of Toremifene 2. Secondary purpose * To evaluate follows after taking 36 months with Letrozole in postmenopausal women with hormone receptor positive breast cancer who complete 5 years of Toremifene. 1. Disease Free Survival rate(DFS)-12 months, 24 months 2. Distant disease free survival rate(DDFS), Overall Survival(OS) * 12 months, 24 months, 36 months c. safety * Change of lipid profiles * Mortality and morbidity due to Cardiovascular disease * Incidence of Fracture * Change of Bone density * Common toxic effect
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
495
Letrozole 2.5mg
Department of Surgery, Asan medical center
Seoul, South Korea
Disease free survival rate
Time frame: 3 years
Disease free survival rate
Time frame: 12 months, 24 months
Distant disease free survival rate
Time frame: 12 months, 24 months, 36 months
Overall survival rate
Time frame: 12, 24, 36 months
Toxicity was assessed by NCI-CTC version 3.0
Time frame: 36 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.