Tamoxifen in the Prevention of Breast Cancer in Hodgkin's Disease Survivors
Hodgkin's Disease, Breast Cancer
About this trial
This is an interventional prevention trial for Hodgkin's Disease focused on measuring Hodgkin's disease, breast cancer prevention, tamoxifen
Eligibility Criteria
Inclusion Criteria: Females diagnosed with Hodgkin's Disease at age < 35 years > 5 years from mantle or chest radiation Current age > 30 years Has completed childbearing Willingness to discontinue use of oral contraceptives or other hormonal contraception for duration of the study Exclusion Criteria: History of secondary malignancy after Hodgkin's disease, except thyroid cancer of basal cell cancer Recurrence of Hodgkin's disease in the 5 years before study entry Current participation in any other cancer prevention study Current or prior use of tamoxifen Current use of coumadin History of deep venous thrombosis, pulmonary embolism, or a condition known to be associated with hypercoagulability History of cerebrovascular accident History of macular degeneration Current use of chemotherapy for benign disease
Sites / Locations
- Massachusetts General Hospital
- Dana-Farber Cancer Institute
Arms of the Study
Arm 1
Experimental
Tamoxifen
Single arm: Tamoxifen 20mg daily