Delmas Pierre D, McClung Michael R, Zanchetta José R, Racewicz Artur, Roux Christian, Benhamou Claude-Laurent, Man Zulema, Eusebio Rachelle A, Beary John F, Burgio David E, Matzkin Ellen, Boonen Steven
INSERM Research Unit 831 and University of Lyon, Lyon, France.
Bone. 2008 Jan;42(1):36-42. doi: 10.1016/j.bone.2007.09.001. Epub 2007 Sep 8.
Risedronate has been shown to be effective in the treatment of postmenopausal osteoporosis when given orally in daily or weekly doses or on 2 consecutive days per month. This randomized, double-blind, multi-center study was designed to assess the efficacy and safety of a single 150 mg risedronate once-a-month oral dose compared with the 5 mg daily regimen.
Women with postmenopausal osteoporosis were randomly assigned to receive risedronate 5 mg daily (n=642) or 150 mg once a month (followed by daily placebo) (n=650) in a double-blind fashion for 2 years. Study drug was taken on an empty stomach at least 30 min before breakfast. Bone mineral density, bone turnover markers, fractures, and adverse events were evaluated. The primary efficacy endpoint was the mean percent change from baseline in lumbar spine bone mineral density after 1 year.
538 patients in the daily group (83.8%) and 556 patients in the once-a-month group (85.5%) completed 1 year. The mean percent change in lumbar spine bone mineral density was 3.4% (95% confidence interval, 3.03% to 3.82%) in the daily group and 3.5% (95% confidence interval, 3.15% to 3.93%) in the once-a-month group. The difference between groups was -0.1% (95% confidence interval, -0.51% to 0.27%). The once-a-month regimen was determined to be non-inferior to the daily regimen based on prospectively defined criteria. The mean percent changes in bone mineral density at sites in the hip (total proximal femur, femoral neck, femoral trochanter) were also similar in both dose groups, as were the changes in biochemical markers of bone turnover. The incidence of adverse events, adverse events leading to withdrawal, and upper gastrointestinal tract adverse events were similar in the 2 treatment groups. Both regimens were well tolerated; the percent of patients who withdrew from treatment as a result of an adverse event was 9.5% in the daily group and 8.6% in the once-a-month group.
Risedronate 150 mg once a month is similar in efficacy and safety to daily dosing and may provide an alternative for patients who prefer once-a-month oral dosing.
已证明,利塞膦酸钠每日或每周口服给药或每月连续2天给药时,对绝经后骨质疏松症的治疗有效。本随机、双盲、多中心研究旨在评估每月口服一次150mg利塞膦酸钠单剂量与每日5mg给药方案相比的疗效和安全性。
绝经后骨质疏松症女性被随机分配,以双盲方式接受每日5mg利塞膦酸钠(n = 642)或每月150mg(随后每日服用安慰剂)(n = 650),为期2年。研究药物在早餐前至少30分钟空腹服用。评估骨矿物质密度、骨转换标志物、骨折和不良事件。主要疗效终点是1年后腰椎骨矿物质密度相对于基线的平均变化百分比。
每日给药组538例患者(83.8%)和每月给药组556例患者(85.5%)完成了1年治疗。每日给药组腰椎骨矿物质密度的平均变化百分比为3.4%(95%置信区间,3.03%至3.82%),每月给药组为3.5%(95%置信区间,3.15%至3.93%)。两组之间的差异为-0.1%(95%置信区间,-0.51%至0.27%)。根据预先定义的标准,确定每月给药方案不劣于每日给药方案。两个剂量组在髋部各部位(股骨近端总体、股骨颈、股骨转子)的骨矿物质密度平均变化百分比也相似,骨转换生化标志物的变化也相似。两个治疗组的不良事件发生率、导致停药的不良事件以及上消化道不良事件相似。两种给药方案耐受性均良好;因不良事件退出治疗的患者百分比在每日给药组为9.5%,在每月给药组为8.6%。
每月一次150mg利塞膦酸钠在疗效和安全性方面与每日给药相似,对于更喜欢每月口服一次给药的患者可能是一种替代选择。