Prevention of Bone Loss by Zoledronic Acid in Premenopausal Women Undergoing Adjuvant Chemotherapy Persist up to One Year following Discontinuing Treatment
| Autor: | Danielle Awad, Dawn L. Hershman, Theresa Shao, Elizabeth Shane, Lois Brafman, Donald J. McMahon, Katherine D. Crew, Serge Cremers |
|---|---|
| Rok vydání: | 2010 |
| Předmět: |
Adult
medicine.medical_specialty Bone density Endocrinology Diabetes and Metabolism Clinical Biochemistry Osteoporosis Breast Neoplasms Context (language use) Zoledronic Acid Biochemistry Bone remodeling Endocrinology Double-Blind Method Bone Density Internal medicine medicine Humans Femoral neck Bone mineral Bone Density Conservation Agents Diphosphonates business.industry Biochemistry (medical) Imidazoles Middle Aged medicine.disease Osteopenia medicine.anatomical_structure Zoledronic acid Premenopause Chemotherapy Adjuvant Original Article Female Bone Remodeling business medicine.drug |
| Zdroj: | The Journal of Clinical Endocrinology & Metabolism. 95:559-566 |
| ISSN: | 1945-7197 0021-972X |
| DOI: | 10.1210/jc.2009-1366 |
| Popis: | Context: Adjuvant chemotherapy is associated with significant reductions in bone mineral density (BMD) in premenopausal women with breast cancer (BC) that is prevented with zoledronic acid (ZA) every 3 months for 1 yr. Objective: The aim of the study was to examine the effect on BMD of discontinuing ZA during the subsequent year. Design: We conducted a randomized, double-blind trial. Patients: Premenopausal women (mean age, 42 yr) undergoing adjuvant chemotherapy for BC participated in the study. Intervention: ZA (4 mg iv every 3 months) vs. placebo was administered for 12 months. Outcome Measures: We measured percentage change in BMD and bone turnover markers at 12 and 24 months (1 yr after last infusion). Results: Of 101 women randomized, 85 completed 12-month and 62 completed 24-month evaluations. In the placebo group, serum C-telopeptide (CTX) increased progressively over the first 12 months, returned toward baseline but remained significantly above baseline by 24 months. Lumbar spine BMD decreased from baseline by 5.5% at 12 and 6.3% at 24 months. Similarly, by 24 months, total hip and femoral neck BMD declined by 2.6 and 2.4%, respectively. In ZA patients, BMD remained stable (P < 0.0001 compared to placebo). Serum CTX declined significantly by 6 months, but returned to baseline by 12 months, remaining there at 24 months. Conclusions: Premenopausal women receiving chemotherapy for BC sustained significant bone loss during the first year, without recovery during the second year. ZA effectively prevented bone loss during the first year of chemotherapy. BMD remained stable 1 yr after completion of ZA. Serum CTX increased significantly by 12 and 24 months. More frequent administration may be required to suppress bone resorption in this patient population. |
| Databáze: | OpenAIRE |
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