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[抑制核因子κB受体活化因子配体治疗骨转移]

[Inhibition of RANK ligand to treat bone metastases].

作者信息

Body Jean-Jacques

机构信息

CHU Brugmann, université libre de Bruxelles (U.L.B.), service de Médecine, 4, place van Gehuchten, B-1020 Bruxelles, Belgique.

出版信息

Bull Cancer. 2013 Nov;100(11):1207-13. doi: 10.1684/bdc.2013.1835.

DOI:10.1684/bdc.2013.1835
PMID:24158618
Abstract

Bone is the most common metastatic site. The skeleton is also the preferential initial metastatic site in breast and prostate carcinomas. Objective complications of bone metastases are named « skeletal-related events » (SREs) and generally include the need for radiotherapy on bone, surgery to bone, pathologic fracture and spinal cord compression. Recent phase III double-blind trials have demonstrated the superiority of denosumab to zoledronic acid for delaying the time to first SRE in patients with breast or prostate cancer and bone metastases. Non-inferiority was shown in the trial including other solid tumors and multiple myeloma. The overall burden of the disease was also significantly reduced in the breast and prostate cancer studies, and in the pre-specified integrated analysis that included all three comparative trials. Denosumab is conveniently administered by subcutaneous injections and is devoid of renal toxicity. However, denosumab induces more cases of hypocalcaemia than zoledronate. Calcium and vitamin D supplementation is recommended during therapy and it is advised to regularly monitor calcium levels during denosumab long-term treatment. There are numerically more cases of osteonecrosis of the jaw, but the differences are not statistically significant between zoledronate and denosumab, whether in the individual studies or in the integrated analysis. Treatment with these potent inhibitors of bone resorption should be progressively 'individualized' to better define the place of intermittent treatments, to decrease the occurrence of toxic effects and to improve the cost-effectiveness ratio of new compounds.

摘要

骨是最常见的转移部位。骨骼也是乳腺癌和前列腺癌优先发生初始转移的部位。骨转移的客观并发症被称为“骨相关事件”(SREs),通常包括对骨进行放疗、骨手术、病理性骨折和脊髓压迫。近期的III期双盲试验已证明,在延缓乳腺癌或前列腺癌伴骨转移患者首次发生SRE的时间方面,地诺单抗优于唑来膦酸。在包括其他实体瘤和多发性骨髓瘤的试验中显示了非劣效性。在乳腺癌和前列腺癌研究以及包括所有三项比较试验的预先指定的综合分析中,疾病的总体负担也显著降低。地诺单抗通过皮下注射给药方便,且无肾毒性。然而,地诺单抗引起低钙血症的病例比唑来膦酸更多。治疗期间建议补充钙和维生素D,并建议在长期使用地诺单抗治疗期间定期监测钙水平。颌骨坏死的病例在数量上更多,但无论是在个体研究还是综合分析中,唑来膦酸和地诺单抗之间的差异均无统计学意义。使用这些强效骨吸收抑制剂进行治疗应逐步“个体化”,以更好地确定间歇治疗的地位,减少毒副作用的发生,并提高新化合物的成本效益比。

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[Inhibition of RANK ligand to treat bone metastases].[抑制核因子κB受体活化因子配体治疗骨转移]
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