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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Lack of Difference in Acute Nephrotoxicity of Intravenous Bisphosphonates Zoledronic Acid and Ibandronate in Women with Breast Cancer and Bone Metastases
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Lack of Difference in Acute Nephrotoxicity of Intravenous Bisphosphonates Zoledronic Acid and Ibandronate in Women with Breast Cancer and Bone Metastases

机译:乳腺癌和骨转移妇女静脉内双膦酸盐唑来膦酸和伊班膦酸钠的急性肾毒性缺乏差异

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Background: More than 50% of patients with advanced breast cancer develop bone metastases that may lead to multiple complications such as pathological fractures, bone pain or hypercalcaemia. The standard treatment, besides endocrine, targeted-therapy or chemotherapy, is the use of bisphosphonates. However, one of their main adverse side-effects is bisphosphonate-induced nephrotoxicity. The mechanism by which the latter occurs is not well-understood, although emerging evidence suggests that the effect of bisphosphonates on the kidney may differ between agents. Patients and Methods: The aim of this evaluation was to compare the renal toxicity of 6 mg ibandronate i.v. versus 4 mg zoledronic acid i.v. over a period of six months in women with breast cancer and bone metastases. A prospective randomized trial was carried out to examine specific kidney and other parameters (alpha 1- and beta 2-microglobulin. albumin, alpha 2-macroglobulin, IgG and C-reactive protein (CRP) generated from spontaneous urine samples from 17 patients of each group. Results: We were unable to find any significant difference between the two treatment groups with regard to renal toxicity. All patients, independently of the applied bisphosphonate, experienced only temporary renal dysfunction without any evidence of irreversible damage in terms of acute nephrotoxicity during the study period, alpha 1-Microglobulin, a marker for proximal tubular damage, in particular, was not differently elevated in either group. Conclusion: Both applied bisphosphonates were found to be well-tolerated and safe with regard to renal toxicity during a six-month treatment period in patients with otherwise healthy kidneys having advanced breast cancer and bone metastases.
机译:背景:超过50%的晚期乳腺癌患者发生骨转移,可能导致多种并发症,例如病理性骨折,骨痛或高钙血症。除内分泌,靶向治疗或化学疗法外,标准治疗方法是使用双膦酸盐。然而,它们的主要不利副作用之一是双膦酸酯诱导的肾毒性。尽管新兴证据表明双膦酸盐对肾脏的作用在不同的药物之间可能不同,但后者发生的机理尚不清楚。患者和方法:这项评估的目的是比较6毫克伊班膦酸钠静脉注射的肾脏毒性。与4 mg唑来膦酸i.v.在患有乳腺癌和骨转移的女性中使用了六个月的时间。进行了一项前瞻性随机试验,以检查特定肾脏和其他参数(α1和β2微球蛋白,白蛋白,α2巨球蛋白,IgG和C反应蛋白(CRP)),这些蛋白是从每位17位患者的自发尿液样本中产生的结果:我们没有发现两个治疗组在肾毒性方面有任何显着差异,所有患者,独立于双膦酸盐应用,仅经历了暂时性肾功能不全,而在急性肾毒性期间没有任何不可逆转的损害证据。在研究期间,α1-微球蛋白(一种特别是近端肾小管损伤的标志物)在两组中均无差异升高结论:发现两种应用的双膦酸盐在六个月内对肾脏毒性具有良好的耐受性和安全性患有晚期乳腺癌和骨转移的健康肾脏患者的治疗期。

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