Department of Nephrology, Wakayama Medical University, Wakayama-city, Japan.
Division of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Tokai University School of Medicine, Isehara-shi, Japan.
Nephrology (Carlton). 2020 Aug;25(8):634-643. doi: 10.1111/nep.13682. Epub 2019 Dec 27.
Secondary hyperparathyroidism (SHPT), a complication of haemodialysis, is commonly treated with calcimimetics. The impact of dialysates containing different calcium (Ca) concentrations on clinical efficacy of calcimimetics are unclear. We examined whether dialysate Ca concentrations influence the efficacy and dosing of etelcalcetide with concomitant drugs.
We performed post hoc analyses of a 52-week, open-label, multicentre study of etelcalcetide in Japanese SHPT patients to determine whether dialysate Ca influences the therapeutic effects of etelcalcetide with concomitant drugs. We evaluated the differences in serum intact parathyroid hormone (iPTH), corrected Ca (cCa) and phosphate levels among three dialysate Ca concentration groups (2.5, 2.75 or 3.0 mEq/L Ca). Tartrate-resistant acid phosphatase 5b (TRACP-5b) and bone alkaline phosphatase (BAP) levels were also compared. Since the dialysate Ca concentration may influence dose adjustment, we assessed the etelcalcetide and concomitant drug doses.
There were no clinically meaningful differences in iPTH, cCa and phosphate levels among the 2.5, 2.75 and 3.0 mEq/L groups (n = 34, 64 and 35, respectively) over 52 weeks. At Week 52, more than 82%, 71% and 67% of patients had iPTH, cCa and phosphate levels within target ranges (60-240 pg/mL, 8.4-10.0 mg/dL and 3.5-6.0 mg/dL, respectively) across the three groups. TRACP-5b and BAP levels decreased by Week 52 regardless of dialysate Ca. Changes in etelcalcetide and concomitant drug doses were generally similar in each group.
The efficacy and dosing of etelcalcetide with concomitant drugs were essentially unaffected by the dialysate Ca concentration. Patients showed improvements in bone hypermetabolism during treatment.
继发性甲状旁腺功能亢进症(SHPT)是血液透析的一种常见并发症,通常使用拟钙剂进行治疗。目前尚不清楚不同钙浓度透析液对拟钙剂临床疗效的影响。我们研究了透析液钙浓度是否会影响依特卡塞与伴随药物联合使用的疗效和剂量。
我们对依特卡塞治疗日本 SHPT 患者的 52 周、开放标签、多中心研究进行了事后分析,以确定透析液钙是否会影响依特卡塞与伴随药物联合使用的治疗效果。我们评估了三种透析液钙浓度(2.5、2.75 或 3.0 mEq/L Ca)组间血清全段甲状旁腺激素(iPTH)、校正钙(cCa)和磷酸盐水平的差异。还比较了抗酒石酸酸性磷酸酶 5b(TRACP-5b)和骨碱性磷酸酶(BAP)水平。由于透析液钙浓度可能会影响剂量调整,我们评估了依特卡塞和伴随药物的剂量。
52 周时,2.5、2.75 和 3.0 mEq/L 组间 iPTH、cCa 和磷酸盐水平无临床意义差异(n=34、64 和 35)。第 52 周时,三组中超过 82%、71%和 67%的患者 iPTH、cCa 和磷酸盐水平均在目标范围内(60-240 pg/mL、8.4-10.0 mg/dL 和 3.5-6.0 mg/dL)。TRACP-5b 和 BAP 水平在第 52 周时均下降,无论透析液钙浓度如何。各组中依特卡塞和伴随药物剂量的变化基本相似。
依特卡塞与伴随药物联合使用的疗效和剂量基本不受透析液钙浓度的影响。患者在治疗过程中骨代谢过度活跃得到改善。