用denosumab减少癌症对骨骼的影响:当前和未来的观点

W. Gradishar, J. Gralow, Stephen N. Jones, H. Collins
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引用次数: 1

摘要

骨转移是晚期癌症的严重并发症。它最常见于转移性乳腺癌和前列腺癌患者,但也发生在大多数其他转移性实体癌中。如果不进行治疗,患者可能会出现并发症,包括顽固性骨痛、高钙血症、骨折、脊髓压迫和/或需要手术或放射治疗干预。2010年,美国食品和药物管理局(fda)批准了一种抑制RANK配体(RANKL)和随后破骨细胞介导的骨破坏的全人源单克隆抗体denosumab,用于预防实体瘤骨转移患者的骨骼相关事件(SREs)。本文综述了denosumab在预防骨转移引起的SREs,治疗激素消融癌症治疗引起的骨质流失方面的作用,并描述了denosumab的安全性和潜在的未来适应症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Minimizing cancer's impact on bone with denosumab: Current and future perspectives
Bone metastasis is a serious complication of advanced cancer. It is most commonly observed in patients with metastatic breast and prostate cancers, but also occurs in most other metastatic solid cancers. Without treatment, patients may experience complications including intractable bone pain, hypercalcemia, fracture, spinal cord compression and/or a requirement for surgical or radiotherapeutic intervention. In 2010, denosumab, a fully human monoclonal antibody that inhibits RANK ligand (RANKL) and subsequent osteoclast-mediated bone destruction, was approved by the Food and Drug Administration for the prevention of skeletal-related events (SREs) in patients with bone metastases from solid tumors. This article reviews the role of denosumab in preventing SREs due to bone metastases, treating bone loss due to hormone-ablative cancer therapies, and describes denosumab’s safety profile and potential future indications under investigation.
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