Zoledronate in Preventing Bone Loss in Premenopausal Women Receiving Chemotherapy After Surgery For Early Stage Breast Cancer
Breast Cancer, Osteoporosis
About this trial
This is an interventional supportive care trial for Breast Cancer focused on measuring osteoporosis, stage I breast cancer, stage II breast cancer
Eligibility Criteria
DISEASE CHARACTERISTICS: Diagnosis of localized breast cancer Stage I or II (T1-3, N0-2, M0) Planned adjuvant chemotherapy (after surgery) of at least 6 months in duration Hormone receptor status: Estrogen receptor and progesterone receptor status known PATIENT CHARACTERISTICS: Age 18 to 50 Sex Female Menopausal status Premenopausal or perimenopausal Performance status Not specified Life expectancy Not specified Hematopoietic Not specified Hepatic Not specified Renal Creatinine less than 2 mg/dL Other No T score of less than 2.0 on bone mineral density (BMD) No fragility fracture No lumbar spine anatomy that would preclude accurate BMD measurement of a minimum of 3 lumbar vertebrae Not pregnant PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy See Disease Characteristics Endocrine therapy Not specified Radiotherapy No concurrent radiotherapy Surgery See Disease Characteristics Other At least 1 month since prior calcitonin At least 12 months since prior bisphosphonates given for more than 1 month duration No concurrent fluoride therapy (10 mg/day or more) No concurrent enrollment in another experimental drug study
Sites / Locations
- Carl and Dorothy Bennett Cancer Center at Stamford Hospital
- Valley Hospital - Paramus
- Herbert Irving Comprehensive Cancer Center at Columbia University