Brown Janet E, Ellis Susan P, Lester James E, Gutcher Sandra, Khanna Tina, Purohit Om-Prakesh, McCloskey Eugene, Coleman Robert E
Academic Unit of Clinical Oncology, Weston Park Hospital, University of Sheffield, United Kingdom.
Clin Cancer Res. 2007 Sep 15;13(18 Pt 1):5406-10. doi: 10.1158/1078-0432.CCR-07-0247.
Bisphosphonates play a central role in the management of bone loss due to a range of disorders, including metastatic bone disease, cancer treatment-induced bone loss, and postmenopausal osteoporosis. With potent bisphosphonates, such as zoledronic acid, it may be possible to maintain efficacy with relatively infrequent administration.
Sixty-six patients who were osteopenic at >1 year following curative cancer therapy received a single i.v. 4 mg dose of the bisphosphonate zoledronic acid. Bone mineral density (BMD) was measured using double-beam X-ray absorptiometry scan and the bone resorption marker N-telopeptide of type II collagen was determined using a chemiluminescence ELISA assay.
The single dose of zoledronic acid induced mean increases in bone BMD at the lumbar spine of 3.1%, 5.2%, and 5.3% and at the total hip of 2.7%, 3.5%, and 4.3% after 12, 24, and 36 months of follow-up, respectively (P < 0.001 at all time points). By 36 months, 84% of patients had achieved increase in BMD at the spine and 90% at the hip. The mean percentage decrease in the bone resorption marker N-telopeptide was approximately 58% at 6 weeks and 42%, 33%, and 31% at 12, 24, and 36 months, respectively (P < 0.001).
A single dose of zoledronic acid in patients with low BMD results in a sustained increase in BMD and a corresponding decrease in bone resorption. Very infrequent administration of zoledronic acid may have clinical benefits in terms of convenience, reduced toxicity, improved compliance, and cost.
双膦酸盐在一系列疾病所致骨质流失的管理中发挥核心作用,这些疾病包括转移性骨病、癌症治疗引起的骨质流失以及绝经后骨质疏松症。使用强效双膦酸盐,如唑来膦酸,可能通过相对不频繁的给药来维持疗效。
66例在根治性癌症治疗1年以上仍存在骨质减少的患者接受了单次静脉注射4mg双膦酸盐唑来膦酸。使用双能X线吸收法扫描测量骨矿物质密度(BMD),并使用化学发光酶联免疫吸附测定法测定骨吸收标志物II型胶原N-端肽。
单次剂量的唑来膦酸在随访12、24和36个月后,分别使腰椎骨密度平均增加3.1%、5.2%和5.3%,全髋骨密度平均增加2.7%、3.5%和4.3%(所有时间点P<0.001)。到36个月时,84%的患者脊柱骨密度增加,90%的患者髋部骨密度增加。骨吸收标志物N-端肽的平均百分比下降在6周时约为58%,在12、24和36个月时分别为42%、33%和31%(P<0.001)。
低骨密度患者单次剂量的唑来膦酸可导致骨密度持续增加以及骨吸收相应减少。非常不频繁地使用唑来膦酸在便利性、降低毒性、提高依从性和成本方面可能具有临床益处。