Breast Cancer Clinical Trial
Official title:
A Feasibility Study of Tamoxifen Prevention of Breast Cancer in Hodgkin's Disease Survivors
The purpose of this study is determine whether or not tamoxifen reduces the chance of Hodgkin's Disease survivors developing breast cancer.
- Patients will receive tamoxifen orally once daily to be taken at home for 1 year. They
will be asked to complete a daily drug log to keep track of the pills taken or missed.
- Patients will also be asked to give a blood/DNA sample which will be stored for
possible further testing for the presence of cancer related genes that are known nor or
discovered in the future.
- Patients will also receive a mammogram that will be reviewed by study officials.
- Side effects will be monitored every 2 months for one year, between visits to the
clinic.
- A follow-up visit will be conducted at the 6 month mark and includes a physical exam,
blood work, health and wellness surveys)
- A follow-up visit will be performed at the 1 year mark and includes a mammogram,
gynecological exam, physical exam, blood work, health and wellness surveys.
- Patients active participation will be for 1 year. However, tamoxifen has been shown to
be effective after a 5-year course in other women at increased risk for breast cancer,
the patient may decide to stay on tamoxifen for 4 additional years.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention
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