Seefried Lothar, Genest Franca, Baumann Jasmin, Heidemeier Anke, Meffert Rainer, Jakob Franz
Orthopedic Center for Musculoskeletal Research, Orthopedic Department, University of Wuerzburg, Wuerzburg, Germany.
Department of Diagnostic and Interventional Radiology, University Hospital Wuerzburg, Wuerzburg, Germany.
J Bone Miner Res. 2022 Mar;37(3):420-427. doi: 10.1002/jbmr.4493. Epub 2022 Jan 13.
Bone marrow lesions (BML) represent areas of deteriorated bone structure and metabolism characterized by pronounced water-equivalent signaling within the trabecular bone on magnetic resonance imaging (MRI). BML are associated with repair mechanisms subsequent to various clinical conditions associated with inflammatory and non-inflammatory injury to the bone. There is no approved treatment for this condition. Bisphosphonates are known to improve bone stability in osteoporosis and other bone disorders and have been used off-label to treat BML. A randomized, triple-blind, placebo-controlled phase III trial was conducted to assess efficacy and safety of single-dose zoledronic acid (ZOL) 5 mg iv with vitamin D 1000 IU/d as opposed to placebo with vitamin D 1000 IU/d in 48 patients (randomized 2:1) with BML. Primary efficacy endpoint was reduction of edema volume 6 weeks after treatment as assessed by MRI. After treatment, mean BML volume decreased by 64.53% (±41.92%) in patients receiving zoledronic acid and increased by 14.43% (±150.46%) in the placebo group (p = 0.007). A decrease in BML volume was observed in 76.5% of patients receiving ZOL and in 50% of the patients receiving placebo. Pain level (visual analogue scale [VAS]) and all categories of the pain disability index (PDI) improved with ZOL versus placebo after 6 weeks but reconciled after 6 additional weeks of follow-up. Six serious adverse events occurred in 5 patients, none of which were classified as related to the study drug. No cases of osteonecrosis or fractures occurred. Therefore, single-dose zoledronic acid 5 mg iv together with vitamin D may enhance resolution of bone marrow lesions over 6 weeks along with reduction of pain compared with vitamin D supplementation only. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).
骨髓病变(BML)表现为骨结构和代谢恶化的区域,其特征是在磁共振成像(MRI)上小梁骨内有明显的水等效信号。BML与各种与骨的炎性和非炎性损伤相关的临床状况后的修复机制有关。目前尚无针对这种病症的获批治疗方法。已知双膦酸盐可改善骨质疏松症和其他骨疾病中的骨稳定性,并已被用于非标签治疗BML。进行了一项随机、三盲、安慰剂对照的III期试验,以评估单剂量静脉注射唑来膦酸(ZOL)5mg加维生素D 1000IU/d与安慰剂加维生素D (1000IU/d)在48例BML患者(随机比例为2:1)中的疗效和安全性。主要疗效终点是治疗6周后通过MRI评估的水肿体积减少。治疗后,接受唑来膦酸的患者平均BML体积减少了64.53%(±41.92%),而安慰剂组增加了14.43%(±150.46%)(p = 0.007)。接受ZOL的患者中有76.5%的BML体积减少,接受安慰剂的患者中有50%的BML体积减少。6周后,与安慰剂相比,ZOL治疗组的疼痛水平(视觉模拟量表[VAS])和疼痛残疾指数(PDI)的所有类别均有所改善,但在额外6周的随访后恢复到基线水平。5例患者发生了6起严重不良事件,均未被分类为与研究药物相关。未发生骨坏死或骨折病例。因此,与仅补充维生素D相比,单剂量静脉注射5mg唑来膦酸加维生素D可能在6周内增强骨髓病变的消退,并减轻疼痛。© 2021作者。《骨与矿物质研究杂志》由Wiley Periodicals LLC代表美国骨与矿物质研究学会(ASBMR)出版。