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Hypercalcemia of malignancy and new treatment options

机译:恶性高钙血症和新的治疗选择

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Hypercalcemia of malignancy affects up to one in five cancer patients during the course of their disease. It is associated with both liquid malignancies, commonly multiple myeloma, leukemia, and non-Hodgkins lymphoma and solid cancers, particularly breast and renal carcinomas as well as squamous cell carcinomas of any organ. The clinical manifestations of hypercalcemia are generally constitutional in nature and not specific to the inciting malignancy. Such physical manifestations can range from malaise to lethargy and confusion. Constipation and anorexia are common. Acute kidney injury is likely the most frequently encountered manifestation of end organ damage. Symptomatology is closely linked to both the absolute elevation of serum calcium levels and the rapidity of calcium rise. The majority of cases are humoral in etiology and related to parathyroid hormone-related protein (PTHrP). Approximately 20% of cases are the result of direct bone metastasis with extra-renal 1,25-dihydroxyvitamin D (calcitriol) and ectopic parathyroid hormone production likely accounting for less than 1% of cases. The diagnosis of hypercalcemia of malignancy is confirmed either by an elevated PTHrP or by an evidence of bone metastasis in the appropriate clinical setting. Treatment is predicated on the patient’s symptoms and absolute serum calcium level. Interventions are aimed at lowering the serum calcium concentration by inhibiting bone resorption and increasing urinary calcium excretion, the former accomplished via bisphosphonate therapy and the latter with aggressive hydration. Novel therapies for refractory disease include denosumab, a monoclonal antibody against the receptor activator of nuclear factor κB ligand, and the calcimimetic cinacalcet. Finally, anti-PTHrP antibodies have been successfully deployed in animal models of disease. Despite the efficacy of the above therapies, hypercalcemia of malignancy portends an ominous prognosis, indicating advanced and often refractory cancer with survival on the order of months.
机译:恶性肿瘤的高钙血症最多影响五分之一的癌症患者。它与液体恶性肿瘤(通常为多发性骨髓瘤,白血病和非霍奇金淋巴瘤)以及实体癌(尤其是乳腺癌和肾癌以及任何器官的鳞状细胞癌)相关。高钙血症的临床表现通常本质上是体质性的,而不是诱发恶性肿瘤的特异性。这种身体表现可能从不适到嗜睡和混乱。便秘和厌食很常见。急性肾脏损伤可能是最常见的末端器官损伤表现。症状学与血清钙水平的绝对升高和钙升高的速度密切相关。大多数病例的病因是体液性的,与甲状旁腺激素相关蛋白(PTHrP)有关。大约20%的病例是由于肾脏外的1,25-二羟基维生素D(骨化三醇)引起的直接骨转移和异位甲状旁腺激素产生的结果,可能少于病例的1%。在适当的临床环境中,PTHrP升高或骨转移的证据可证实对恶性高钙血症的诊断。根据患者的症状和绝对血清钙水平进行治疗。干预旨在通过抑制骨吸收和增加尿钙排泄来降低血清钙浓度,前者通过双膦酸盐治疗实现,后者通过积极的水合作用。难治性疾病的新疗法包括狄诺塞麦(denosumab),抗核因子κB配体受体激活剂的单克隆抗体和拟钙剂cinacalcet。最后,抗PTHrP抗体已成功部署在疾病的动物模型中。尽管上述疗法有效,但恶性高钙血症预示了预后不良,表明晚期癌症且通常是难治性癌症,生存期约为数月。

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