scholarly journals Zoledronic acid and skeletal complications in patients with solid tumors and bone metastases

Cancer ◽  
2008 ◽  
Vol 113 (6) ◽  
pp. 1438-1445 ◽  
Author(s):  
Hind T. Hatoum ◽  
Swu-Jane Lin ◽  
Mathew R. Smith ◽  
Victoria Barghout ◽  
Allan Lipton
2007 ◽  
Vol 1 (1) ◽  
pp. 92-98
Author(s):  
Fred Saad ◽  
Yin-Miao Chen ◽  
Donald M. Gleason ◽  
Joseph Chin

2004 ◽  
Vol 10 (18) ◽  
pp. 6397S-6403S ◽  
Author(s):  
Allan Lipton ◽  
Alejandro Colombo-Berra ◽  
Ronald M. Bukowski ◽  
Lee Rosen ◽  
Ming Zheng ◽  
...  

2007 ◽  
Vol 25 (18_suppl) ◽  
pp. 19669-19669
Author(s):  
M. K. Altundag ◽  
M. Dincer ◽  
H. Harputluoglu ◽  
S. Aksoy ◽  
Y. Ozisik ◽  
...  

19669 Background: Zoledronic acid (ZA) delays the onset or reduces the incidence of skeletal complications in breast cancer patients with bone metastases. However there are few data on the long-term renal safety of ZA. Methods: We retrospectively evaluated 43 breast cancer patients with bone metastases who received ZA more than 24 months. The following parameters measured prior to first ZA use and after the last dose of ZA administration were compared: serum creatinine (SCr), blood urea nitrogen (BUN), alkaline phosphatase (ALP), calcium (Ca), and phosphorous (P). Results: Forty-three breast cancer patients with documented bone metastases were evaluated. Median age at the start of treatment was 53 years (range, 37 to 77). Median overall duration of ZA administration was 36 months (25 to 62). There were no statistically significant differences in the pre- and post-treatment levels of SCr, BUN, Ca and P. However, ALP levels after long-term ZA administration were decreased significantly (P <0.05). Conclusion: More than 24 months of ZA administration did not adversely affect the renal function. ZA can be used safely in breast cancer patients with bone metastases beyond 2 years. [Table: see text] No significant financial relationships to disclose.


2005 ◽  
Vol 23 (32) ◽  
pp. 8219-8224 ◽  
Author(s):  
M. Dror Michaelson ◽  
Matthew R. Smith

Bone metastases are a major cause of morbidity for men with prostate cancer. Complications of bone metastases include pain, fractures, and spinal cord compression. Although they appear osteoblastic by radiographic imaging, most bone metastases are characterized by excess osteoclast number and activity. In addition, pathologic osteoclast activation is associated with increased risk of skeletal complications. Zoledronic acid, a potent inhibitor of osteoclast activity, differentiation, and survival, decreases the risk of skeletal complications in men with androgen-independent prostate cancer and bone metastases. Other bisphosphonates, including pamidronate and clodronate, seem to be ineffective in this setting. The reduction in risk of skeletal complications with zoledronic acid must be weighed against potential adverse effects. Additional studies are needed to determine the optimal timing, schedule, and duration of treatment in men with bone metastases as well as the potential role of bisphosphonates in other settings including the prevention of bone metastases.


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