Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, USA.
Department of Medicine, University of Auckland, Auckland, New Zealand.
J Bone Miner Res. 2022 Jan;37(1):21-28. doi: 10.1002/jbmr.4434. Epub 2021 Sep 28.
Zoledronic acid (ZOL) as a yearly infusion is effective in reducing fracture risk. An acute-phase reaction (APR), consisting of flu-like symptoms within 3 days after infusion, is commonly seen. The objective of this analysis was to investigate whether APR occurrence influences drug efficacy. This analysis uses data from the 3-year randomized clinical trial, Health Outcomes and Reduced Incidence with Zoledronic Acid Once Yearly-Pivotal Fracture Trial (HORIZON-PFT). APRs were identified as adverse events within 3 days of first infusion with higher frequency in ZOL than placebo. To compare mean 3-year change in bone mineral density (BMD) in ZOL versus placebo, among women with and without APR, t tests were used. Logistic regression was used to examine the relationship between APR occurrence and odds of incident morphometric vertebral fracture. Cox regression was used to determine the risk of nonvertebral and hip fractures for women with versus without APR. Logistic and Cox models were used to determine the risk of incident fracture in ZOL versus placebo for women with and without an APR. The analysis included 3862 women in the ZOL group and 3852 in placebo, with 42.4% in ZOL versus 11.8% in placebo experiencing an APR. The difference in BMD mean change for ZOL versus placebo was similar for women with and without an APR (all p interaction >0.10). Among ZOL women, those with APR had 51% lower vertebral fracture risk than those without (odds ratio [OR] = 0.49, p < 0.001). A similar but nonsignificant trend was observed for nonvertebral and hip fracture (relative hazard [RH] = 0.82, p = 0.10; RH = 0.70, p = 0.22, respectively). There was a greater treatment-related reduction in vertebral fracture risk among women with APR (OR = 0.19) than those without (OR = 0.38) (p interaction = 0.01). Our results suggest that women starting ZOL who experience an APR will have a larger reduction in vertebral fracture risk with ZOL. © 2021 American Society for Bone and Mineral Research (ASBMR).
唑来膦酸(ZOL)作为每年一次的输注治疗,可有效降低骨折风险。输注后 3 天内常出现急性相反应(APR),表现为流感样症状。本分析的目的是研究 APR 的发生是否会影响药物疗效。本分析使用了为期 3 年的随机临床试验,即唑来膦酸每年一次-关键骨折试验(HORIZON-PFT)的疗效和降低发生率的结果的数据。APR 被定义为首次输注后 3 天内的不良事件,ZOL 组的发生率高于安慰剂组。为了比较 ZOL 组与安慰剂组在 APR 患者和非 APR 患者中 3 年的平均骨密度(BMD)变化,使用 t 检验进行比较。采用逻辑回归分析 APR 发生与新发形态计量学椎体骨折之间的关系。采用 Cox 回归分析 APR 患者与非 APR 患者的非椎体骨折和髋部骨折风险。采用 Cox 回归分析 APR 患者与非 APR 患者的非椎体骨折和髋部骨折风险。采用逻辑回归和 Cox 模型分析 APR 患者与非 APR 患者 ZOL 与安慰剂的新发骨折风险。该分析纳入了 ZOL 组的 3862 名女性和安慰剂组的 3852 名女性,ZOL 组的 APR 发生率为 42.4%,安慰剂组为 11.8%。对于 APR 患者和非 APR 患者,ZOL 组与安慰剂组的 BMD 平均变化差异相似(所有 p 交互作用>0.10)。在 ZOL 组女性中,发生 APR 的患者的椎体骨折风险比未发生 APR 的患者低 51%(比值比[OR]为 0.49,p<0.001)。非椎体骨折和髋部骨折也观察到相似但无统计学意义的趋势(相对危险度[RH]分别为 0.82,p=0.10;RH 为 0.70,p=0.22)。与未发生 APR 的患者相比,发生 APR 的患者的椎体骨折风险的治疗相关降低幅度更大(OR=0.19)(OR=0.38)(p 交互作用=0.01)。我们的结果表明,开始接受 ZOL 治疗的女性,如果出现 APR,将有更大的 ZOL 治疗降低椎体骨折风险。