Renal safety of zoledronic acid with thalidomide in patients with myeloma: A pharmacokinetic and safety sub-study

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Abstract

Background: Cases of impaired renal function have been reported in patients who had been treated with both zoledronic acid and thalidomide for myeloma. Hence, we conducted a safety study of zoledronic acid and thalidomide in myeloma patients participating in a trial of maintenance therapy. Methods: Twenty-four patients who were enrolled in a large randomized trial of thalidomide vs no thalidomide maintenance therapy for myeloma, in which all patients also received zoledronic acid, were recruited to a pharmacokinetic and renal safety sub-study, and followed for up to 16 months. Results: No significant differences by Wilcoxon rank-sum statistic were found in zoledronic acid pharmacokinetics or renal safety for up to 16 months in patients randomized to thalidomide or not. Conclusion: In myeloma patients receiving maintenance therapy, the combination of zoledronic acid and thalidomide appears to confer no additional renal safety risks over zoledronic acid alone. © 2008 Spencer et al; licensee BioMed Central Ltd.

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Spencer, A., Roberts, A., Kennedy, N., Ravera, C., Cremers, S., Bilic, S., … Lynch, K. (2008). Renal safety of zoledronic acid with thalidomide in patients with myeloma: A pharmacokinetic and safety sub-study. BMC Clinical Pharmacology, 8. https://doi.org/10.1186/1472-6904-8-2

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