Ristow Oliver, Gerngroß Carlos, Schwaiger Markus, Hohlweg-Majert Bettina, Kehl Victoria, Jansen Heike, Hahnefeld Lilian, Koerdt Steffen, Otto Sven, Pautke Christoph
Ludwig-Maximilians Universität München, Goethestr. 70, D-80336 Munich, Germany; Medizin & Aesthetik, Clinic for Oral and Maxillofacial and Plastic Surgery, Lenbachplatz 2a, D-80333 Munich, Germany.
Technische Universität München, Department of Nuclear Medicine, Ismaninger Straße 22, D-81675 Munich, Germany.
Br J Oral Maxillofac Surg. 2014 Apr;52(4):308-13. doi: 10.1016/j.bjoms.2014.01.021. Epub 2014 Feb 26.
Osteonecrosis of the jaw as a result of treatment with receptor activators of nuclear factor kappa-B ligand (RANKL) inhibitors (denosumab) is a new type of bony necrosis, the exact pathogenesis of which is unknown. Our aim was to find out whether the turnover of bone in the jaw is increased after denosumab has been given compared with other skeletal sites, and if that turnover might have a role in denosumab-related osteonecrosis of the jaw (DRONJ). Bone scintigraphic images of 45 female patients with breast cancer and bone metastases were analysed retrospectively, and divided into 3 groups: those given denosumab, those given a bisphosphonate, and a control group (n=15 in each). All patients had bone scintigraphy before treatment (T0) and during the course of treatment after 12 (T1) and 24 (T2) months. The data were analysed quantitatively using 6 preset bony regions of interest. There was similar turnover of bone in the mandible compared with other skeletal sites (such as the femur), while the maxilla showed significantly higher turnover. None of the bony regions investigated showed any significant changes after the bisphosphonate had been given. There was a tendency to increase bone turnover in those patients taking denosumab. The bone turnover of the jawbone is not overtly changed either by a bisphosphonate or denosumab, so it seems unlikely that oversuppression of bony turnover in the jawbones plays an important part either in the pathogenesis of DRONJ or in the bisphosphonate-related osteonecrosis of the jaw (BRONJ).
因使用核因子κB受体活化因子配体(RANKL)抑制剂(地诺单抗)治疗导致的颌骨坏死是一种新型骨坏死,其确切发病机制尚不清楚。我们的目的是弄清楚与其他骨骼部位相比,给予地诺单抗后颌骨的骨转换是否增加,以及这种转换是否可能在与地诺单抗相关的颌骨坏死(DRONJ)中起作用。对45例患有乳腺癌和骨转移的女性患者的骨闪烁显像图像进行回顾性分析,并分为3组:接受地诺单抗治疗的患者、接受双膦酸盐治疗的患者和对照组(每组n = 15)。所有患者在治疗前(T0)以及治疗过程中的12个月(T1)和24个月(T2)时均进行了骨闪烁显像。使用6个预设的骨感兴趣区域对数据进行定量分析。与其他骨骼部位(如股骨)相比,下颌骨的骨转换相似,而上颌骨的骨转换明显更高。给予双膦酸盐后,所研究的任何骨区域均未显示出任何显著变化。服用地诺单抗的患者有骨转换增加的趋势。双膦酸盐或地诺单抗均未明显改变颌骨的骨转换,因此,颌骨骨转换的过度抑制似乎不太可能在DRONJ或双膦酸盐相关颌骨坏死(BRONJ)的发病机制中起重要作用。