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伊班膦酸盐,一种用于治疗骨质疏松症、骨转移和恶性肿瘤高钙血症的实验性静脉注射双膦酸盐。

Ibandronate, an experimental intravenous bisphosphonate for osteoporosis, bone metastases, and hypercalcemia of malignancy.

作者信息

Guay David R P

机构信息

Department of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, 55455, USA.

出版信息

Pharmacotherapy. 2006 May;26(5):655-73. doi: 10.1592/phco.26.5.655.

Abstract

Ibandronate is an experimental intravenous bisphosphonate under study for the prevention or treatment of osteoporosis and skeletal complications of bone metastases, as well as hypercalcemia of malignancy. To review the data on this drug, PubMed/MEDLINE was searched for pertinent studies in English; data from January 1986-October 2005 were reviewed. In preclinical studies, ibandronate was an extremely potent bisphosphonate compared with its predecessors and was active in all animal models of human postmenopausal and corticosteroid-associated osteoporosis. Similar to other bisphosphonates, ibandronate exhibits antitumor activity and prevents or reduces bone metastases. Forty to fifty percent of the dose is bound to bone; renal clearance of unchanged drug accounts for 70% of total body clearance. Early clinical trials demonstrated efficacy and tolerability of intravenous ibandronate in the prevention or treatment of postmenopausal and corticosteroid-associated osteoporosis when administered once every 3 months. Intravenous ibandronate also reduces skeletal complications of bone metastases, including pain, although the cumulative dose used is much higher than that used in osteoporosis, as the drug is administered every 3-4 weeks. Single doses of intravenous ibandronate are probably also effective in the treatment of hypercalcemia of malignancy. The major tolerability issue with intravenous bisphosphonates is renal safety, thus the drugs generally require infusion (e.g., 0.25 hr for zoledronic acid, 2-24 hrs for pamidronate). However, intravenous ibandronate can be administered by bolus injection over a few minutes without an elevated risk of nephrotoxicity. The experimental intravenous dosage is 2 mg every 3 months for treatment or prevention of osteoporosis, and 2-6 mg every 3-4 weeks or in a single dose for treatment of bone metastases or hypercalcemia of malignancy, respectively. Ibandronate can be used in the presence of severe renal impairment with proper dosage adjustment. The drug will be an interesting addition to the available drugs for osteoporosis, bone metastases, and hypercalcemia of malignancy. Studies of intravenous ibandronate as an adjunctive treatment for cancers that tend to metastasize to bone are under way. Whether intravenous ibandronate will be a therapeutic advance is best answered by randomized, controlled trials. These are ongoing and should provide data with which to make better-informed choices concerning intravenous bisphosphonates.

摘要

伊班膦酸钠是一种正在进行试验的静脉用双膦酸盐药物,正用于研究预防或治疗骨质疏松症、骨转移的骨骼并发症以及恶性肿瘤引起的高钙血症。为了回顾关于这种药物的数据,我们在PubMed/MEDLINE中检索了英文相关研究;对1986年1月至2005年10月的数据进行了回顾。在临床前研究中,与之前的双膦酸盐相比,伊班膦酸钠是一种极其有效的双膦酸盐,在所有人类绝经后和皮质类固醇相关骨质疏松症的动物模型中均有活性。与其他双膦酸盐类似,伊班膦酸钠具有抗肿瘤活性,可预防或减少骨转移。40%至50%的剂量与骨结合;原形药物的肾清除率占全身清除率的70%。早期临床试验表明,每3个月静脉注射一次伊班膦酸钠在预防或治疗绝经后和皮质类固醇相关骨质疏松症方面具有疗效和耐受性。静脉注射伊班膦酸钠还可减少骨转移的骨骼并发症,包括疼痛,尽管所用的累积剂量远高于骨质疏松症治疗时的剂量,因为该药物每3至4周给药一次。单次静脉注射伊班膦酸钠可能对治疗恶性肿瘤引起的高钙血症也有效。静脉用双膦酸盐的主要耐受性问题是肾脏安全性,因此这些药物通常需要静脉输注(例如,唑来膦酸输注0.25小时,帕米膦酸输注2至24小时)。然而,静脉注射伊班膦酸钠可在几分钟内推注给药,而不会增加肾毒性风险。治疗或预防骨质疏松症的试验性静脉剂量为每3个月2毫克,治疗骨转移或恶性肿瘤引起的高钙血症的剂量分别为每3至4周2至6毫克或单次剂量。在适当调整剂量的情况下,严重肾功能损害患者也可使用伊班膦酸钠。对于骨质疏松症、骨转移和恶性肿瘤引起的高钙血症,该药物将是现有药物中一个有趣的补充。关于静脉注射伊班膦酸钠作为倾向于转移至骨的癌症辅助治疗的研究正在进行中。静脉注射伊班膦酸钠是否会带来治疗进展,最好通过随机对照试验来回答。这些试验正在进行中,应该会提供数据,以便就静脉用双膦酸盐做出更明智的选择。

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