Department of Medicine, CHU Brugmann, Université Libre de Bruxelles, Place A.Van Gehuchten 4, 1020, Brussels, Belgium.
Kantonsspital Graubünden, Loëstrasse 170, CH-7000, Chur, Switzerland.
BMC Urol. 2018 Sep 20;18(1):81. doi: 10.1186/s12894-018-0393-9.
Most patients with advanced prostate cancer develop bone metastases, which often result in painful and debilitating skeletal-related events. Inhibitors of bone resorption, such as bisphosphonates and denosumab, can each reduce the incidence of skeletal-related events and delay the progression of bone pain. However, these agents are associated with an increased risk of hypocalcaemia, which, although often mild and transient, can be serious and life-threatening. Here we provide practical advice on managing the risk of hypocalcaemia in patients with advanced prostate cancer who are receiving treatment with bone resorption inhibitors. Relevant references for this review were identified through searches of PubMed with the search terms 'prostate cancer', 'bone-targeted agents', 'anti-resorptive agents', 'bisphosphonates', 'zoledronic acid', 'denosumab', 'hypocalcaemia', and 'hypocalcemia'. Additional references were suggested by the authors.
Among patients with advanced cancer receiving a bisphosphonate or denosumab, hypocalcaemia occurs most frequently in those with prostate cancer, although it can occur in patients with any tumour type. Consistent with its greater ability to inhibit bone resorption, denosumab has shown superiority in the prevention of skeletal-related events in patients with bone metastases from solid tumours. Consequently, denosumab is more likely to induce hypocalcaemia than the bisphosphonates. Likewise, various bisphosphonates have differing potencies for the inhibition of bone resorption, and thus the risk of hypocalcaemia varies between different bisphosphonates. Other risk factors for the development of hypocalcaemia include the presence of osteoblastic metastases, vitamin D deficiency, and renal insufficiency. Hypocalcaemia can lead to treatment interruption, but it is both preventable and manageable. Serum calcium concentrations should be measured, and any pre-existing hypocalcaemia should be corrected, before starting treatment with inhibitors of bone resorption. Once treatment has started, concomitant administration of calcium and vitamin D supplements is essential. Calcium concentrations should be monitored during treatment with bisphosphonates or denosumab, particularly in patients at high risk of hypocalcaemia. If hypocalcaemia is diagnosed, patients should receive treatment with calcium and vitamin D.
With preventative strategies and treatment, patients with prostate cancer who are at risk of, or who develop, hypocalcaemia should be able to continue to benefit from treatment with bisphosphonates or denosumab.
大多数晚期前列腺癌患者会发生骨转移,这常常导致痛苦和虚弱的骨骼相关事件。骨吸收抑制剂,如双膦酸盐和地舒单抗,都可以降低骨骼相关事件的发生率并延缓骨痛的进展。然而,这些药物会增加低钙血症的风险,尽管这种情况通常是轻微和短暂的,但也可能是严重的、危及生命的。在这里,我们为接受骨吸收抑制剂治疗的晚期前列腺癌患者管理低钙血症风险提供了实用建议。本综述的相关参考文献是通过在 PubMed 中使用“前列腺癌”、“骨靶向药物”、“抗吸收剂”、“双膦酸盐”、“唑来膦酸”、“地舒单抗”、“低钙血症”和“低钙血症”等关键词进行搜索确定的。作者还提出了其他参考文献。
在接受双膦酸盐或地舒单抗治疗的晚期癌症患者中,低钙血症最常发生在前列腺癌患者中,但也可能发生在任何肿瘤类型的患者中。由于其更强的抑制骨吸收能力,地舒单抗在预防骨转移肿瘤患者的骨骼相关事件方面显示出优越性。因此,地舒单抗比双膦酸盐更有可能引起低钙血症。同样,各种双膦酸盐对骨吸收的抑制作用也有不同的效力,因此不同双膦酸盐之间发生低钙血症的风险也不同。低钙血症的其他危险因素包括存在成骨转移、维生素 D 缺乏和肾功能不全。低钙血症可导致治疗中断,但它既可以预防,也可以治疗。在开始使用骨吸收抑制剂之前,应测量血清钙浓度,并纠正任何先前存在的低钙血症。一旦开始治疗,同时给予钙和维生素 D 补充剂是必不可少的。在使用双膦酸盐或地舒单抗治疗期间,应监测钙浓度,尤其是在有发生低钙血症高风险的患者中。如果诊断出低钙血症,应给予患者钙和维生素 D 治疗。
通过预防策略和治疗,有发生或已经发生低钙血症风险的前列腺癌患者应该能够继续从双膦酸盐或地舒单抗治疗中获益。