Khosla Sundeep, Burr David, Cauley Jane, Dempster David W, Ebeling Peter R, Felsenberg Dieter, Gagel Robert F, Gilsanz Vincente, Guise Theresa, Koka Sreenivas, McCauley Laurie K, McGowan Joan, McKee Marc D, Mohla Suresh, Pendrys David G, Raisz Lawrence G, Ruggiero Salvatore L, Shafer David M, Shum Lillian, Silverman Stuart L, Van Poznak Catherine H, Watts Nelson, Woo Sook-Bin, Shane Elizabeth
J Bone Miner Res. 2007 Oct;22(10):1479-91. doi: 10.1359/jbmr.0707onj.
ONJ has been increasingly suspected to be a potential complication of bisphosphonate therapy in recent years. Thus, the ASBMR leadership appointed a multidisciplinary task force to address key questions related to case definition, epidemiology, risk factors, diagnostic imaging, clinical management, and future areas for research related to the disorder. This report summarizes the findings and recommendations of the task force.
The increasing recognition that use of bisphosphonates may be associated with osteonecrosis of the jaw (ONJ) led the leadership of the American Society for Bone and Mineral Research (ASBMR) to appoint a task force to address a number of key questions related to this disorder.
A multidisciplinary expert group reviewed all pertinent published data on bisphosphonate-associated ONJ. Food and Drug Administration drug adverse event reports were also reviewed.
A case definition was developed so that subsequent studies could report on the same condition. The task force defined ONJ as the presence of exposed bone in the maxillofacial region that did not heal within 8 wk after identification by a health care provider. Based on review of both published and unpublished data, the risk of ONJ associated with oral bisphosphonate therapy for osteoporosis seems to be low, estimated between 1 in 10,000 and <1 in 100,000 patient-treatment years. However, the task force recognized that information on incidence of ONJ is rapidly evolving and that the true incidence may be higher. The risk of ONJ in patients with cancer treated with high doses of intravenous bisphosphonates is clearly higher, in the range of 1-10 per 100 patients (depending on duration of therapy). In the future, improved diagnostic imaging modalities, such as optical coherence tomography or MRI combined with contrast agents and the manipulation of image planes, may identify patients at preclinical or early stages of the disease. Management is largely supportive. A research agenda aimed at filling the considerable gaps in knowledge regarding this disorder was also outlined.
近年来,颌骨坏死(ONJ)越来越被怀疑是双膦酸盐治疗的一种潜在并发症。因此,美国骨与矿物质研究学会(ASBMR)领导层任命了一个多学科特别工作组,以解决与病例定义、流行病学、危险因素、诊断成像、临床管理以及该疾病相关的未来研究领域等关键问题。本报告总结了特别工作组的调查结果和建议。
越来越多的人认识到双膦酸盐的使用可能与颌骨坏死(ONJ)有关,这促使美国骨与矿物质研究学会(ASBMR)领导层任命了一个特别工作组,以解决与该疾病相关的一些关键问题。
一个多学科专家组审查了所有关于双膦酸盐相关ONJ的相关已发表数据。还审查了美国食品药品监督管理局的药物不良事件报告。
制定了病例定义,以便后续研究能够报告相同的情况。特别工作组将ONJ定义为颌面部区域存在暴露的骨,在医疗保健提供者识别后8周内未愈合。基于对已发表和未发表数据的审查,与口服双膦酸盐治疗骨质疏松症相关的ONJ风险似乎较低,估计在每10000至每100000患者治疗年中少于1例。然而,特别工作组认识到关于ONJ发病率的信息正在迅速演变,实际发病率可能更高。接受高剂量静脉注射双膦酸盐治疗的癌症患者中ONJ的风险明显更高,每100名患者中有1 - 10例(取决于治疗持续时间)。未来,改进的诊断成像方式,如光学相干断层扫描或结合造影剂和图像平面操作的MRI,可能会识别处于疾病临床前或早期阶段的患者。管理主要是支持性的。还概述了一项旨在填补关于该疾病的大量知识空白的研究议程。