[Bone and calcium metabolism associated with malignancy. Bone management of prostate cancer in the novel anti-androgen era.]

Clinical calcium Pub Date : 2018-01-01 DOI:CliCa181115351544
Hisashi Matsushima
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Abstract

Androgen deprivation therapy(ADT)is a standard systemic therapy for prostate cancer. ADT induces bone loss(ADTIBL)and muscle loss(sarcopenia)leading to falls and farctures. There are 2 aims in bone management of prostate cancer:one is to prevent fragility fractures in patients without bone metastasis and the other is to prevent symptomatic skeletal events(SSE)which are pathologic fractures, spinal compression, radiation to bones and surgery to bones. Bone fractures and SSE are both correlated with worse overall survival(OS). Concomitant use of novel anti-androgens further increases the risk of falls and fractures. The earlier and appropiriate intervention with vitamin D and bone modifying agents(BMA)is necessary to prevent treatment related bone fractures and SSE. Bone management algorithm aids to decide the timing and doses of BMA. As for sarcopenia physical exercise and life style advices are important. Because abiraterone with glucocorticoid therapy induces stronger bone resorption, it is recommended to start denosumab simultaneously. Ra-223, bone seeking radiopharmaceuticals should not be used with abiraterone and predonisone because of high incidence of fracture and death.

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与恶性肿瘤相关的骨和钙代谢。新抗雄激素时代前列腺癌的骨管理。
雄激素剥夺疗法(ADT)是前列腺癌的标准全身治疗方法。ADT诱导骨质流失(ADTIBL)和肌肉流失(肌肉减少症),导致跌倒和骨折。前列腺癌的骨管理有两个目标:一是防止无骨转移的患者发生脆性骨折,二是预防病理性骨折、脊柱压迫、骨放射和骨手术等症状性骨骼事件。骨折和SSE均与较差的总生存期(OS)相关。同时使用新型抗雄激素进一步增加跌倒和骨折的风险。早期适当的维生素D和骨修饰剂(BMA)干预对于预防治疗相关骨折和SSE是必要的。骨管理算法有助于确定BMA的时间和剂量。对于肌肉减少症,体育锻炼和生活方式的建议很重要。由于阿比特龙联合糖皮质激素治疗可诱导更强的骨吸收,建议同时开始使用地诺单抗。Ra-223,寻骨放射性药物不应与阿比特龙和强的松一起使用,因为骨折和死亡的发生率很高。
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