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甲状旁腺激素替代治疗甲状旁腺功能减退症的疗效和安全性:第 3 阶段 PaTHway 试验的 26 周结果。

Efficacy and Safety of Parathyroid Hormone Replacement With TransCon PTH in Hypoparathyroidism: 26-Week Results From the Phase 3 PaTHway Trial.

机构信息

Endocrinology, Metabolism, and Geriatrics, McMaster University, Hamilton, Ontario, Canada.

Endocrinology, Columbia University, New York, New York, USA.

出版信息

J Bone Miner Res. 2023 Jan;38(1):14-25. doi: 10.1002/jbmr.4726. Epub 2022 Nov 12.

Abstract

Conventional therapy for hypoparathyroidism consisting of active vitamin D and calcium aims to alleviate hypocalcemia but fails to restore normal parathyroid hormone (PTH) physiology. PTH replacement therapy is the ideal physiologic treatment for hypoparathyroidism. The double-blind, placebo-controlled, 26-week, phase 3 PaTHway trial assessed the efficacy and safety of PTH replacement therapy for hypoparathyroidism individuals with the investigational drug TransCon PTH (palopegteriparatide). Participants (n = 84) were randomized 3:1 to once-daily TransCon PTH (initially 18 μg/d) or placebo, both co-administered with conventional therapy. The study drug and conventional therapy were titrated according to a dosing algorithm guided by serum calcium. The composite primary efficacy endpoint was the proportion of participants at week 26 who achieved normal albumin-adjusted serum calcium levels (8.3-10.6 mg/dL), independence from conventional therapy (requiring no active vitamin D and ≤600 mg/d of calcium), and no increase in study drug over 4 weeks before week 26. Other outcomes of interest included health-related quality of life measured by the 36-Item Short Form Survey (SF-36), hypoparathyroidism-related symptoms, functioning, and well-being measured by the Hypoparathyroidism Patient Experience Scale (HPES), and urinary calcium excretion. At week 26, 79% (48/61) of participants treated with TransCon PTH versus 5% (1/21) wiplacebo met the composite primary efficacy endpoint (p < 0.0001). TransCon PTH treatment demonstrated a significant improvement in all key secondary endpoint HPES domain scores (all p < 0.01) and the SF-36 Physical Functioning subscale score (p = 0.0347) compared with placebo. Additionally, 93% (57/61) of participants treated with TransCon PTH achieved independence from conventional therapy. TransCon PTH treatment normalized mean 24-hour urine calcium. Overall, 82% (50/61) treated with TransCon PTH and 100% (21/21) wiplacebo experienced adverse events; most were mild (46%) or moderate (46%). No study drug-related withdrawals occurred. In conclusion, TransCon PTH maintained normocalcemia while permitting independence from conventional therapy and was well-tolerated in individuals with hypoparathyroidism. © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

摘要

甲状旁腺功能减退症的常规治疗包括活性维生素 D 和钙,旨在缓解低钙血症,但无法恢复正常甲状旁腺激素 (PTH) 生理功能。PTH 替代疗法是甲状旁腺功能减退症的理想生理治疗方法。双盲、安慰剂对照、26 周、3 期 PaTHway 试验评估了研究药物 TransCon PTH(palopegteriparatide)治疗甲状旁腺功能减退症患者的疗效和安全性。参与者(n=84)按 3:1 随机分为每日一次 TransCon PTH(初始剂量为 18μg/d)或安慰剂组,两者均与常规疗法联合使用。根据血清钙指导的剂量算法调整研究药物和常规疗法。主要复合疗效终点是第 26 周时达到正常白蛋白校正血清钙水平(8.3-10.6mg/dL)、脱离常规疗法(无需活性维生素 D 和≤600mg/d 钙)以及在第 26 周前 4 周内研究药物无增加的参与者比例。其他感兴趣的结果包括通过 36 项简短表格调查 (SF-36) 测量的健康相关生活质量,通过甲状旁腺功能减退症患者体验量表 (HPES) 测量的甲状旁腺功能减退症相关症状、功能和幸福感,以及尿钙排泄。第 26 周时,接受 TransCon PTH 治疗的 61 名参与者中有 79%(48/61),而接受安慰剂治疗的参与者有 5%(1/21)符合主要复合疗效终点(p<0.0001)。与安慰剂相比,TransCon PTH 治疗显著改善了所有关键次要终点 HPES 域评分(均 p<0.01)和 SF-36 生理功能子量表评分(p=0.0347)。此外,93%(57/61)接受 TransCon PTH 治疗的参与者脱离了常规治疗。TransCon PTH 治疗使 24 小时尿钙均值正常化。总体而言,接受 TransCon PTH 治疗的 61 名参与者中有 82%(50/61)和接受安慰剂治疗的 21 名参与者中有 100%(21/21)发生了不良事件;大多数为轻度(46%)或中度(46%)。未发生与研究药物相关的停药事件。总之,TransCon PTH 在维持血钙正常的同时允许脱离常规治疗,并在甲状旁腺功能减退症患者中耐受良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1ea/10099823/9b9313acd7e3/JBMR-38-14-g004.jpg

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