OsteoRheuma Bern, Bern, Switzerland.
Department of Rheumatology and Immunology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
J Bone Miner Res. 2022 Feb;37(2):340-348. doi: 10.1002/jbmr.4472. Epub 2021 Nov 30.
Osteonecrosis of the jaw (ONJ) is a rare but serious adverse event associated with antiresorptive treatment. There is little evidence regarding the incidence of ONJ among patients with osteoporosis who are treated with denosumab versus bisphosphonates (BPs). The aim of this study was to determine the risk of ONJ in a real-world population. Subjects who underwent at least one dual-energy X-ray absorptiometry (DXA) examination were included in the osteoporosis register of the Swiss Society of Rheumatology between January 1, 2015, and September 30, 2019. Statistical analyses included incidence rates, rate ratios, and hazard ratios for ONJ, considering sequential therapies and drug holidays as covariates. Among 9956 registered patients, 3068 (89% female, median age 69 years [63 to 76]) were treated with BPs or denosumab for a cumulative duration of 11,101 and 4236 patient-years, respectively. Seventeen cases of ONJ were identified: 12 in patients receiving denosumab at the time of ONJ diagnosis and 5 in patients receiving oral or intravenous BP therapy. The diagnosis of ONJ was confirmed by independent and blinded maxillofacial surgeons, using the American Association of Oral and Maxillofacial Surgeons case definition of ONJ. The incidence of ONJ per 10,000 observed patient-years was 28.3 in patients receiving denosumab and 4.5 in patients with BP-associated ONJ, yielding a rate ratio of 6.3 (95% confidence interval [CI] 2.1 to 22.8), p < 0.001. Nine of 12 patients who developed ONJ during denosumab treatment had been pretreated with BPs, but none of the 5 patients with BP-related ONJ had previously received denosumab. The risk of ONJ was higher in patients receiving denosumab therapy compared with BPs (hazard ratio 3.49, 95% CI 1.16 to 10.47, p = 0.026). Previous BP therapy before switching to denosumab may be an additional risk factor for ONJ development. © 2021 American Society for Bone and Mineral Research (ASBMR).
颌骨骨坏死(ONJ)是一种罕见但严重的与抗吸收治疗相关的不良事件。关于接受地舒单抗与双膦酸盐(BPs)治疗的骨质疏松症患者中 ONJ 的发生率,证据很少。本研究的目的是确定真实人群中 ONJ 的风险。
2015 年 1 月 1 日至 2019 年 9 月 30 日,瑞士风湿病学会骨质疏松症登记处纳入了至少进行过一次双能 X 线吸收法(DXA)检查的患者。统计分析包括考虑序贯治疗和药物假期为协变量时,ONJ 的发生率、比率和风险比。在登记的 9956 例患者中,3068 例(89%为女性,中位年龄 69 岁[63 至 76])接受了 BP 或地舒单抗治疗,累积治疗时间分别为 11101 和 4236 患者年。共发现 17 例 ONJ 病例:12 例在诊断为 ONJ 时正在接受地舒单抗治疗,5 例在接受口服或静脉 BP 治疗时发生。ONJ 的诊断由独立和盲法的颌面外科医生根据美国口腔颌面外科协会的 ONJ 病例定义进行确认。接受地舒单抗治疗的患者每 10000 例观察患者年的 ONJ 发生率为 28.3,BP 相关 ONJ 患者的发生率为 4.5,比率为 6.3(95%置信区间[CI] 2.1 至 22.8),p<0.001。在接受地舒单抗治疗期间发生 ONJ 的 12 例患者中有 9 例曾接受过 BP 预处理,但在 5 例 BP 相关 ONJ 患者中没有一例曾接受过地舒单抗治疗。与 BP 相比,接受地舒单抗治疗的患者发生 ONJ 的风险更高(风险比 3.49,95%CI 1.16 至 10.47,p=0.026)。在转为地舒单抗治疗前接受 BP 治疗可能是发生 ONJ 的另一个危险因素。
© 2021 美国骨骼与矿物质研究协会(ASBMR)。