Prescrire Int. 2006 Jun;15(83):90-3.
(1) Patients who require dialysis for chronic renal failure develop phosphocalcium metabolic disorders that often lead to secondary hyperparathyroidism. Standard treatment consists of a phosphate chelator and vitamin D, along with the use of an appropriate calcium concentration in the dialysis bath, but is difficult to manage. (2) Parathyroid cancer is a rare malignancy frequently associated with hypercalcaemia. (3) Cinacalcet is a calcimimetic agent that reduces the parathormone level. Clinical evaluation includes more than a dozen dose-finding studies and clinical trials. The optimal dose seems to range from 30 to 180 mg/day and varies widely from one patient to another. (4) 3 double-blind placebo-controlled trials, lasting for a maximum of one year and involving a total of 1136 dialysis patients with chronic renal failure, showed no improvement in quality of life with cinacalcet. The target parathormone level was reached by 40% of patients on cinacalcet versus 5% of patients on placebo, while the effects of cinacalcet on calcium levels (-7%) and phosphate levels (-8%) were modest. No impact on bone complications is mentioned in available reports. (5) The assessment of treatment of parathyroid cancer is limited to one ongoing non comparative trial involving 21 patients. (6) During clinical trials, 11% of dialysis patients had low parathormone levels, creating a risk of adynamic bone disease and fractures, but available data are sparse. (7) Two-thirds of patients receiving cinacalcet have episodes of hypocalcaemia, which may in part account for reports of seizures (1.4% of patients), nausea (31%) and vomiting (27%). Many adverse effects seen in animal studies have not been adequately investigated in the clinical setting, such as an increase in the QT interval, thyroid disorders, and sexual dysfunction. Cinacalcet is a powerful CYP 2D6 inhibitor and is also metabolised by isoenzymes CYP 3A4 and CYP 1A2, creating an increased risk of drug interactions. (8) In practice, treatment with cinacalcet seems difficult to manage and to provide only limited benefits. Available assessment reports leave many questions unanswered, and this is a further reason not to use this product outside of clinical trials, either after failure of phosphate chelator and vitamin D therapy (especially as an alternative to surgery) or in parathyroid cancer.
(1)需要进行透析治疗慢性肾衰竭的患者会出现磷钙代谢紊乱,这常常导致继发性甲状旁腺功能亢进。标准治疗包括使用磷酸盐螯合剂和维生素D,以及在透析液中使用适当的钙浓度,但治疗起来较为困难。(2)甲状旁腺癌是一种罕见的恶性肿瘤,常与高钙血症相关。(3)西那卡塞是一种钙敏感受体激动剂,可降低甲状旁腺激素水平。临床评估包括十几项剂量探索研究和临床试验。最佳剂量似乎在30至180毫克/天之间,且患者之间差异很大。(4)3项双盲安慰剂对照试验,最长持续一年,共纳入1136例慢性肾衰竭透析患者,结果显示使用西那卡塞并未改善生活质量。使用西那卡塞的患者中有40%达到了目标甲状旁腺激素水平,而使用安慰剂的患者中这一比例为5%,同时西那卡塞对钙水平(-7%)和磷水平(-8%)的影响较小。现有报告中未提及对骨并发症的影响。(5)对甲状旁腺癌治疗的评估仅限于一项正在进行的非对照试验,该试验涉及21例患者。(6)在临床试验期间,11%的透析患者甲状旁腺激素水平较低,存在发生动力缺失性骨病和骨折的风险,但现有数据较少。(7)接受西那卡塞治疗的患者中有三分之二会出现低钙血症,这可能部分解释了癫痫发作(1.4%的患者)、恶心(31%)和呕吐(27%)的报告。动物研究中发现的许多不良反应在临床环境中尚未得到充分研究,如QT间期延长、甲状腺疾病和性功能障碍。西那卡塞是一种强效的CYP 2D6抑制剂,也通过同工酶CYP 3A4和CYP 1A2代谢,增加了药物相互作用的风险。(8)在实际应用中,西那卡塞治疗似乎难以管理,且仅能带来有限的益处。现有评估报告留下了许多未解答的问题,这也是不在临床试验之外使用该产品的另一个原因,无论是在磷酸盐螯合剂和维生素D治疗失败后(尤其是作为手术的替代方案)还是在甲状旁腺癌中。