Lewin J, Thomas D
Peter MacCallum Cancer Centre, Melbourne, Australia.
Drugs Today (Barc). 2013 Nov;49(11):693-700. doi: 10.1358/dot.2013.49.11.2064725.
Giant cell tumor of bone (GCTB) is an osteolytic, usually benign neoplasm characterized by infiltration with osteoclast-like giant cells, and the osteoclast differentiation factor receptor activator of nuclear factor kappa-B ligand (RANKL) is heavily involved in its pathogenesis. Denosumab belongs to a new class of drugs that inhibit RANKL. Prior to denosumab, multimodality treatment in refractory, recurrent and metastatic GCTB has shown variable results. Recent phase II data have demonstrated denosumab's activity with regard to disease and symptom control, without significant adverse effects. On the basis of this data, the FDA approved denosumab for the treatment of patients whose GCTB is unresectable, or when surgery is likely to result in severe morbidity. Ongoing questions remain, including the optimal scheduling, patient selection, use in the adjuvant setting and long-term toxicity concerns.
骨巨细胞瘤(GCTB)是一种溶骨性肿瘤,通常为良性,其特征是有破骨细胞样巨细胞浸润,核因子κB受体活化因子配体(RANKL)这种破骨细胞分化因子在其发病机制中起重要作用。地诺单抗属于一类新型的抑制RANKL的药物。在使用地诺单抗之前,难治性、复发性和转移性GCTB的多模式治疗效果不一。近期的II期数据表明地诺单抗在控制疾病和症状方面有活性,且无明显不良反应。基于这些数据,美国食品药品监督管理局(FDA)批准地诺单抗用于治疗GCTB无法切除或手术可能导致严重并发症的患者。仍存在一些未解决的问题,包括最佳给药方案、患者选择、辅助治疗中的应用以及长期毒性问题。