|
|
||||||||
Sign In to gain access to subscriptions and/or personal tools. |
|||||||||
PHARMACOKINETICS AND PHARMACODYNAMICS |
From Novartis Pharmaceuticals Corporation, East Hanover, New Jersey (Dr. Skerjanec, Dr. Hsu, Ms. Ravera, Dr. Schran, Dr. Seaman); Cedars-Sinai Medical Center and UCLA School of Medicine, Los Angeles (Dr. Berenson); Hamilton Regional Cancer Center, Hamilton, Canada (Dr. Major); Jewish General Hospital, Montreal, Canada (Dr. Miller); and Novartis Pharma AG, Basel, Switzerland (Dr. Waldmeier)
An open-label pharmacokinetic and pharmacodynamic study of zoledronic acid (ZometaTM) was performed in 19 cancer patients with bone metastases and known, varying levels of renal function. Patients were stratified according to creatinine clearance (CLcr) into different groups of normal (CLcr > 80 mL/min), mildly (CLcr = 50-80 mL/min), or moderately/severely impaired (CLcr = 10-50 mL/min) renal function. Three intravenous infusions of 4 mg zoledronic acid were administered at 1-month intervals between doses. Plasma concentrations and amounts excreted in urine were determined in all subjects, and 4 patients were administered 14C-labeled zoledronic acid to assess excretion and distribution of drug in whole blood. In general, the drug was well tolerated by the patients. Mean area under the plasma concentration versus time curve and mean concentration immediately after cessation of drug infusion were lower, and mean amounts excreted in urine over 24 hours from start of infusion were higher in normal subjects than in those with impaired renal function (36% vs. 28% of excreted dose), although the differences were not significant. Furthermore, with repeated doses, there was no evidence of drug accumulation in plasma or changes in drug exposure in any of the groups, nor was there any evidence of changes in renal function status. Serum levels of markers of bone resorption (serum C-telopeptide and N-telopeptide) were noticeably reduced after each dose of zoledronic acid across all three renal groups. It was concluded that in patients with mildly to moderately reduced renal function, dosage adjustment of zoledronic acid is likely not necessary.
![]()
CiteULike
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
![]() |
T. TANAKA, H. KAWASHIMA, K. OHNISHI, K. MATSUMURA, R. YOSHIMURA, M. MATSUYAMA, K. KURATSUKURI, and T. NAKATANI Indirect Antitumor Effects of Bisphosphonates on Prostatic LNCaP Cells Co-cultured with Bone Cells Anticancer Res, April 1, 2009; 29(4): 1089 - 1094. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. D. Toussaint, G. J. Elder, and P. G. Kerr Bisphosphonates in Chronic Kidney Disease; Balancing Potential Benefits and Adverse Effects on Bone and Soft Tissue Clin. J. Am. Soc. Nephrol., January 1, 2009; 4(1): 221 - 233. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. M. Weiss, U. Pfaar, A. Schweitzer, H. Wiegand, A. Skerjanec, and H. Schran Biodistribution and Plasma Protein Binding of Zoledronic Acid Drug Metab. Dispos., October 1, 2008; 36(10): 2043 - 2049. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. R. Reid Pathogenesis of Osteonecrosis of the Jaw IBMS BoneKEy, February 1, 2008; 5(2): 69 - 77. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Peng, Y. Sohara, R. A. Moats, M. D. Nelson Jr., S. G. Groshen, W. Ye, C. P. Reynolds, and Y. A. DeClerck The Activity of Zoledronic Acid on Neuroblastoma Bone Metastasis Involves Inhibition of Osteoclasts and Tumor Cell Survival and Proliferation Cancer Res., October 1, 2007; 67(19): 9346 - 9355. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Bergner, D. M. Henrich, M. Hoffmann, A. Honecker, G. Mikus, B. Nauth, D. Nagel, and M. Uppenkamp Renal Safety and Pharmacokinetics of Ibandronate in Multiple Myeloma Patients With or Without Impaired Renal Function J. Clin. Pharmacol., August 1, 2007; 47(8): 942 - 950. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Ory, F. Blanchard, S. Battaglia, F. Gouin, F. Redini, and D. Heymann Zoledronic Acid Activates the DNA S-Phase Checkpoint and Induces Osteosarcoma Cell Death Characterized by Apoptosis-Inducing Factor and Endonuclease-G Translocation Independently of p53 and Retinoblastoma Status Mol. Pharmacol., January 1, 2007; 71(1): 333 - 343. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Wakchoure, M. A. Merrell, W. Aldrich, T. Millender-Swain, K. W. Harris, P. Triozzi, and K. S. Selander Bisphosphonates Inhibit the Growth of Mesothelioma Cells In vitro and In vivo. Clin. Cancer Res., May 1, 2006; 12(9): 2862 - 2868. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Caraglia, D. Santini, M. Marra, B. Vincenzi, G. Tonini, and A. Budillon Emerging anti-cancer molecular mechanisms of aminobisphosphonates. Endocr. Relat. Cancer, March 1, 2006; 13(1): 7 - 26. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Munier, V. Gras, M. Andrejak, N. Bernard, M.-J. Jean-Pastor, S. Gautier, M. Biour, and Z. Massy Zoledronic Acid and Renal Toxicity: Data from French Adverse Effect Reporting Database Ann. Pharmacother., July 1, 2005; 39(7): 1194 - 1197. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Lussier, A. G. Huskey, and R. K. Portenoy Adjuvant Analgesics in Cancer Pain Management Oncologist, September 1, 2004; 9(5): 571 - 591. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |