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肾脏病与透析肾移植杂志 ›› 2025, Vol. 34 ›› Issue (6): 501-510.DOI: 10.3969/j.issn.1006⁃298X.2025.06.001

• 论著 •    下一篇

西那卡塞治疗血液透析患者继发性甲状旁腺功能亢进:一项分层分析研究

  

  • 出版日期:2025-12-28 发布日期:2025-12-29

Cinacalcet in hemodialysis patients with secondary hyperparathyroidism: a stratified study

  • Online:2025-12-28 Published:2025-12-29

摘要: 目的:探究西那卡塞在伴不同严重程度继发性甲状旁腺功能亢进(SHPT)的维持性血液透析(MHD)患者中的疗效与安全性。方法:本研究为开放标签、平行分组、多中心研究,包括第一阶段为期 32 周的药物干预研究以及第二阶段为期 20 周的试验后随访。根据基线全段甲状旁腺激素(iPTH)水平将患者分为轻度(≥300 pg/mL 且 < 600 pg/mL)、中度(≥600 pg/mL 且 < 900 pg/mL)或重度(≥900 pg/mL)SHPT 组。在第一阶段,受试者在常规治疗的基础上口服西那卡塞,剂量从 25mg 逐步递增至 100mg,以达到 iPTH ≥150 pg/ml 且 < 300 pg/mL 的目标值。在第二阶段,患者可自行选择是否继续服用西那卡塞。主要疗效指标为第 20 周和第 32 周 iPTH 达标率。结果:共纳入 750 例 SHPT 患者,其中轻度组 275 例(36.7%),中度组 224 例(29.9%),重度组 251 例(33.4%)。治疗 20 周,三组患者 iPTH 达标率分别为 35.5%、28.3% 和 12.4%(P<0.001)。治疗 32 周时,这一比例分别上升至 41.2%、27.7% 和 15.9%(P<0.001)。西那卡塞治疗显著降低了各组患者的血钙、血磷和 FGF-23 水平。随着 SHPT 程度加重,患者需要的西那卡塞治疗剂量增加,低钙血症发生率也随之升高。试验后随访 20 周,分别有 40.0% 和 47.6% 的患者仍维持了 iPTH 和成纤维细胞生长因子 23(FGF-23)较基线下降≥30%。结论:MHD 患者在 SHPT 早期阶段启动西那卡塞治疗有助于提高疗效,应重视对西那卡塞不良反应的观察及处理。

关键词: font-family:Inter, -apple-system, BlinkMacSystemFont, ", font-size:16px, background-color:#FFFFFF, ">西那卡塞、维持性血液透析、继发性甲状旁腺功能亢进、甲状旁腺激素、成纤维细胞生长因子 23

Abstract: Objective: To evaluate the efficacy and safety of cinacalcet in maintenance hemodialysis patients with varying severity of secondary hyperparathyroidism (SHPT). Methodology: This open-label, parallel-group, multicenter study consisted of a 32-week cohort study followed by a 20-week post-trial follow-up. Patients were stratified by baseline iPTH levels into mild (≥300 pg/mL and <600 pg/mL), moderate (≥600 pg/mL and <900 pg/mL), or severe (≥900 pg/mL) categories. During the cohort study, participants received oral cinacalcet once daily, titrated from 25mg to 100mg, to achieve a target iPTH of ≥150 pg/ml and <300 pg/mL alongside conventional therapy. In the post-trial follow-up, patients chose whether to continue cinacalcet at their own expense. The primary efficacy outcome was the proportion of patients achieving the target iPTH level at weeks 20 and 32. Results: A total of 750 patients were enrolled, including 275 with mild, 224 with moderate, and 251 with severe SHPT. The primary efficacy outcome was achieved by 35.5%, 28.3%, and 12.4% of patients in the mild-to-severe groups, respectively, at week 20 (P<0.001). By week 32, these rates increased to 41.2%, 27.7%, and 15.9%, respectively (P<0.001). Cinacalcet significantly reduced serum calcium, phosphorus, and fibroblast growth factor 23 (FGF-23) levels across all SHPT severity groups. Higher cinacalcet doses and increased hypocalcemia incidence were observed in patients with more severe SHPT. During the post-trial follow-up, 40.0% and 47.6% of patients maintained ≥30% reductions in iPTH and FGF-23, respectively. Conclusion: These findings support initiating cinacalcet treatment at an early stage of SHPT in patients on maintenance hemodialysis. However, attention should be paid to treatment-related adverse events.

Key words: font-family:Inter, -apple-system, BlinkMacSystemFont, ", font-size:16px, background-color:#FFFFFF, ">cinacalcet, maintenance hemodialysis, secondary hyperparathyroidism, parathyroid hormone, fibroblast growth factor 23