Denosumab and giant cell tumour of bone-a review and future management considerations

被引:62
|
作者
Xu, S. F. [1 ]
Adams, B. [2 ]
Yu, X. C. [1 ]
Xu, M. [1 ]
机构
[1] Gen Hosp JiNan Mil Reg, Dept Orthopaed, Jinan 250031, Peoples R China
[2] Medstar Washington Hosp Ctr, Orthopaed Oncol Dept, Inst Canc, Washington, DC USA
关键词
Denosumab; giant cell tumour of bone; receptor activator of nuclear factor kappa B ligand; RANKL; bone turnover; BREAST-CANCER; PROSTATE-CANCER; RECEPTOR ACTIVATOR; MULTIPLE-MYELOMA; ZOLEDRONIC ACID; SOLID TUMORS; LONG BONES; PHASE-II; KAPPA-B; METASTASES;
D O I
10.3747/co.20.1497
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Giant cell tumour of bone (GCTB) is one type of giant-cell-rich bone lesion characterized by the presence of numerous multinucleated osteoclast-type giant cells. Giant cells are known to express RANKL (receptor activator of nuclear factor kappa B ligand) and are responsible for the aggressive osteolytic nature of the tumour. No available treatment option is definitively effective in curing this disease, especially in surgically unsalvageable cases. In recent years, several studies of denosumab in patients with advanced or unresectable GCTB have shown objective changes in tumour composition, reduced bony destruction, and clinical benefit. Denosumab is a fully human monoclonal antibody that targets and binds with high affinity and specificity to RANKL. Several large phase III studies have shown that denosumab is more effective than bisphosphonates in reducing skeletal morbidity arising from a wide range of tumours and that it can delay bone metastasis. The relevant articles are reviewed here. The controversies related to the future use of denosumab in the treatment of GCTB are discussed.
引用
收藏
页码:E442 / E447
页数:6
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