Gatti D, Adami S
University Hospital of Valeggio, University of Verona, Italy.
Drugs Aging. 1999 Oct;15(4):285-96. doi: 10.2165/00002512-199915040-00004.
Bisphosphonates are pyrophosphate analogues, in which the oxygen in P-O-P has been replaced by a carbon, resulting in a P-C-P structure. They are characterised by a strong anti-osteoclastic activity and for this pharmacological property they are now considered the treatment of choice for Paget's disease of the bone, malignant hypercalcaemia and bone metastases. Etidronate, clodronate and pamidronate have been registered in several countries for these indications. Etidronate and alendronate are also extensively used for the prevention and treatment of postmenopausal and senile osteoporosis. In this article, we review the most recent findings on the newest bisphosphonates, which will become available in the near future. The aminobisphosphonate risedronate is undergoing a huge programme of clinical development for the treatment of osteoporosis. In a study of the prevention of early postmenopausal bone loss, oral risedronate 5 mg fully prevented the bone loss observed in the placebo group. Similar effects have been observed with an intermittent dosage regimen of oral risedronate 30 mg/day for 2 out of 12 weeks, which corresponds to 5 mg/day in terms of cumulative dose. With lower doses [5 mg on alternate fortnights (2 weeks)] the prevention of bone loss was half that observed with continuous 5 mg/day therapy, indicating that this might not yet be the maximum effective dose. The use of intermittent intravenous bisphosphonates for osteoporosis therapy has been pioneered by studies with clodronate, pamidronate and alendronate. This treatment regimen has been chosen for an extensive clinical development programme for ibandronate. In a phase 2 study, this new bisphosphonate was administered as an intravenous bolus (0.25, 0.5, 1 or 2 mg) every 3 months for a year, with increases in spinal bone mass of 5.2%. Tiludronate, alendronate and risedronate have been recently introduced for the treatment of Paget's disease of bone. Daily doses of tiludronate 400 mg, alendronate 40 mg and risedronate 30 mg for 3 to 6 months have been shown to be superior to etidronate 400 mg/day. The intravenous administration of ibandronate, zoledronate and alendronate (40 mg, 10 mg and 5 mg, respectively) have achieved the normalisation of serum alkaline phosphatase in more than 70% of the patients and these treatments may provide an alternative for patients intolerant oral bisphosphonates. Intravenous ibandronate has been also developed for the treatment of hypercalcaemia of malignancy. The effective doses ranged from 2 to 4 mg. Zoledronate appears to be the most powerful bisphosphonate under investigation, and the effective doses used in cancer hypercalcaemia are as low as 1 to 2 mg. The new generation of bisphosphonates are likely to increase clinical options in terms of administration regimens, but their real advantage over those already available in terms of clinical efficacy remains uncertain.
双膦酸盐是焦磷酸盐类似物,其中P-O-P中的氧被碳取代,形成P-C-P结构。它们的特点是具有强大的抗破骨细胞活性,基于这种药理特性,它们现在被认为是治疗骨Paget病、恶性高钙血症和骨转移的首选药物。依替膦酸、氯膦酸和帕米膦酸已在多个国家注册用于这些适应症。依替膦酸和阿仑膦酸也广泛用于预防和治疗绝经后和老年性骨质疏松症。在本文中,我们综述了关于最新双膦酸盐的最新研究结果,这些双膦酸盐将在不久的将来上市。氨基双膦酸盐利塞膦酸正在进行一项用于治疗骨质疏松症的大型临床开发计划。在一项预防绝经后早期骨质流失的研究中,口服5毫克利塞膦酸完全预防了安慰剂组中观察到的骨质流失。口服利塞膦酸30毫克/天,每12周中有2周采用间歇给药方案,在累积剂量方面相当于5毫克/天,也观察到了类似的效果。使用较低剂量[每两周(2周)交替服用5毫克]预防骨质流失的效果是连续5毫克/天治疗的一半,这表明这可能还不是最大有效剂量。氯膦酸、帕米膦酸和阿仑膦酸的研究开创了间歇性静脉注射双膦酸盐治疗骨质疏松症的先河。这种治疗方案已被用于伊班膦酸的一项广泛临床开发计划。在一项2期研究中,这种新的双膦酸盐每3个月静脉推注一次(0.25、0.5、1或2毫克),持续一年,脊柱骨量增加了5.2%。替鲁膦酸、阿仑膦酸和利塞膦酸最近已被用于治疗骨Paget病。每日服用400毫克替鲁膦酸、40毫克阿仑膦酸和30毫克利塞膦酸,持续3至6个月,已被证明优于每日服用400毫克依替膦酸。静脉注射伊班膦酸、唑来膦酸和阿仑膦酸(分别为40毫克、10毫克和5毫克)使70%以上的患者血清碱性磷酸酶恢复正常,这些治疗方法可能为不耐受口服双膦酸盐的患者提供一种替代方案。静脉注射伊班膦酸也已被开发用于治疗恶性肿瘤引起的高钙血症。有效剂量范围为2至4毫克。唑来膦酸似乎是正在研究的最有效的双膦酸盐,用于癌症高钙血症的有效剂量低至1至2毫克。新一代双膦酸盐在给药方案方面可能会增加临床选择,但它们在临床疗效方面相对于现有药物的真正优势仍不确定。