Silverberg S J, Rubin M R, Faiman C, Peacock M, Shoback D M, Smallridge R C, Schwanauer L E, Olson K A, Klassen P, Bilezikian J P
College of Physicians and Surgeons, Columbia University, 630 West 168th Street, New York, New York 10032, USA.
J Clin Endocrinol Metab. 2007 Oct;92(10):3803-8. doi: 10.1210/jc.2007-0585. Epub 2007 Jul 31.
Management of inoperable parathyroid carcinoma presents a challenge because until recently, effective medical therapy was not available. Morbidity and mortality result primarily from severe hypercalcemia. We assessed the ability of the calcimimetic cinacalcet HCl to reduce serum calcium in patients with parathyroid carcinoma as well as its effect on PTH concentrations, bone turnover markers, safety, and health-related quality of life variables.
Twenty-nine patients with parathyroid carcinoma were enrolled in this open-label, single-arm study consisting of titration and maintenance phases. Cinacalcet doses were titrated (30 mg twice daily to 90 mg four times daily) for 16 wk or until serum calcium was no more than 10.0 mg/dl. The study endpoint was the proportion of patients with at least a 1 mg/dl reduction in serum calcium at the end of the titration phase (responders).
Mean (+/- se) serum calcium (14.1 +/- 0.4 mg/dl) and PTH (697 +/- 94 pg/ml) were markedly elevated at baseline. At the end of the titration period, serum calcium was reduced by at least 1 mg/dl in 62% of patients (mean decline to 12.4 +/- 0.5 mg/dl). In the 18 responders, serum calcium fell from 15.0 +/- 0.5 to 11.2 +/- 0.3 mg/dl (P < 0.001). The greatest reductions in serum calcium were observed in patients with highest baseline calcium levels. PTH levels decreased, but not significantly, to 635 +/- 73 pg/ml (-4.6%). Adverse events included nausea, vomiting, headache, and fracture.
Cinacalcet effectively reduces hypercalcemia in approximately two thirds of patients with inoperable parathyroid carcinoma and may represent an important new treatment option for these patients.
不可手术切除的甲状旁腺癌的治疗颇具挑战,因为直到最近,仍没有有效的药物治疗方法。发病率和死亡率主要源于严重的高钙血症。我们评估了拟钙剂盐酸西那卡塞降低甲状旁腺癌患者血清钙的能力,以及其对甲状旁腺激素(PTH)浓度、骨转换标志物、安全性和健康相关生活质量变量的影响。
29例甲状旁腺癌患者参与了这项开放标签、单臂研究,该研究包括滴定阶段和维持阶段。西那卡塞剂量进行滴定(从每日两次30毫克至每日四次90毫克),持续16周或直至血清钙不超过10.0毫克/分升。研究终点是滴定阶段结束时血清钙至少降低1毫克/分升的患者比例(反应者)。
基线时,血清钙均值(±标准误)为(14.1±0.4毫克/分升),PTH为(697±94皮克/毫升),均显著升高。滴定期结束时,62%的患者血清钙至少降低了1毫克/分升(平均降至12.4±0.5毫克/分升)。在18例反应者中,血清钙从15.0±0.5降至11.2±0.3毫克/分升(P<0.001)。血清钙降低幅度最大的是基线钙水平最高的患者。PTH水平下降,但不显著,降至635±73皮克/毫升(-4.6%)。不良事件包括恶心、呕吐、头痛和骨折。
西那卡塞可有效降低约三分之二不可手术切除的甲状旁腺癌患者的高钙血症,可能是这些患者重要的新治疗选择。