4.3 Article

Zoledronic acid: A new parenteral bisphosphonate

Journal

CLINICAL THERAPEUTICS
Volume 25, Issue 11, Pages 2669-2708

Publisher

EXCERPTA MEDICA INC
DOI: 10.1016/S0149-2918(03)80327-2

Keywords

zoledronic acid; bisphosphonates; hypercalcemia; bone metastases

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Background: Inhibition of bone resorption using bisphosphonates is an important step in palliation of complications of advanced cancer, such as hypercalcemia and metastatic bone disease. Objective: The goal of this article was to describe the pharmacologic properties of zoledronic acid (zoledronate) and discuss findings from preclinical and clinical studies of its use in skeletal disorders. Methods: Relevant English-language literature was identified using the terms zoledronic acid, zoledronate, Zometa, and 118072-93-8 through searches of MEDLINE (1966-june 2003) and International Pharmaceutical Abstracts (1970-June 2003), and abstract proceedings from the American Society of Clinical Oncology (1997-2002). Results: Zoledronic acid is a nitrogen-containing bisphosphonate that inhibits bone resorption. It is indicated for the treatment of hypercalcemia of malignancy and for the treatment of patients with multiple myeloma or documented metastasis from solid tumors, in conjunction with standard antineoplastic therapy The recommended dosage is 4 mg via IV over greater than or equal to15 minutes every 3 or 4 weeks. Compared with pamidronate 90 mg, zoledronic acid 4 and 8 mg provided a higher complete response rate for hypercalcemia of malignancy by day 10 (88.4% and 86.7% vs 69.7%: P = 0.002 and P = 0.015) and longer duration of action (median Lime to relapse, 30 and 40 days vs 17 days- P = 0.001 and P = 0.007). In patients with breast cancer or multiple myeloma, zoledronic acid was as effective as pamidronate in delaying time to a first skeletal-related event (373 days vs 363 days). In patients with hormone-refractory prostate cancer and bone metastases, zoledronic acid 4 mg reduced the proportion of patients who experienced a skeletal-related event (33% vs 44% with placebo; P = 0.021) or a skeletal fracture (13% vs 22% with placebo; P = 0.015). In patients with bone metastases from solid tumors. zoledronic acid delayed the median time to a first skeletal-related event (230 days vs 163 days with placebo, P = 0.023). Common adverse events include fever, nausea, constipation, fatigue, and bone pain. Conclusion: Zoledronic acid is an effective and generally well-tolerated treatment for hypercalcemia of malignancy and skeletal complications of metastatic hone disease. (Clin Ther. 2003-,25:2669-2708) Copyright (C) 2003 Excerpta Medica, Inc.

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