Project Details
Description
DESCRIPTION (provided by applicant): In the United States, more than 2
million women are living with a history of breast cancer. Because of past
advances in chemotherapy, the vast majority of women diagnosed with breast
cancer will survive for many years, but they will also have increased risk for
long-term complications related to estrogen deficiency, lymph node dissection,
and other effects of chemotherapy on health tissue Evidence suggests that
women who survive breast cancer have an increased risk for osteoporosis. This
risk is highest for premenopausal women who become menopausal with
chemotherapy. However, controversy exists regarding the extent of bone loss,
and only a few studies have evaluated mechanisms to prevent it. A double-
blind randomized control trial of weekly alendronate in premenopausal women
treated with adjuvant chemotherapy for breast cancer will be performed to
define and compare the changes in BMD and bone turnover that occur during and
after adjuvant chemotherapy for breast cancer. We expect to characterize the
natural history of bone loss during chemotherapy and define risk factors that
contribute to this loss in newly diagnosed premenopausal breast cancer
patients. By defining factors that predict accelerated bone loss we hope to
help guide preventive therapy. With the results of this trial, cost-
effectiveness of bisphosphonate treatment will be modeled. We expect that
bisphosphonates will significantly reduce the rate of bone loss in this
patient population and that bisphosphonate use for the prevention of
osteoporosis and its related complications will be cost-effective. The
training portion of this proposal includes regular mentoring with Dr. Karen
Antman and Dr. Elizabeth Shane; extensive interaction with Dr. Alfred Neugut,
Dr. Victor Grann, and Dr. Richard Gralla; and continued formal coursework at
the Mailman School of Public Health at Columbia University. My goal as an
independent investigator is to conduct clinical research that will identify
approaches to cancer treatment that will minimize toxic effects, prevent long-
term complications, and maximize survival, quality of life, and cost-
effectiveness.
Status | Finished |
---|---|
Effective start/end date | 7/1/02 → 6/30/08 |
Funding
- National Cancer Institute: US$133,761.00
- National Cancer Institute: US$133,489.00
- National Cancer Institute: US$133,761.00
- National Cancer Institute: US$133,760.00
- National Cancer Institute: US$133,761.00
ASJC Scopus Subject Areas
- Cancer Research
- Oncology
- Rheumatology
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