Sustained improvement in renal function with palopegteriparatide in adults with chronic hypoparathyroidism: 2-year results from the phase 3 PaTHway-trial.

IF 6.5 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Lars Rejnmark, Elvira O Gosmanova, Aliya A Khan, Stuart Sprague, Dolores M Shoback, Lynn Kohlmeier, Mishaela R Rubin, Andrea Palermo, Peter Schwarz, Claudia Gagnon, Elena Tsourdi, Yasuhiro Takeuchi, Noriko Makita, Yasuo Imanishi, Neil Gittoes, Juan J Díez, Caroline Prot-Bertoye, Bryant Lai, Carol Zhao, Jenny Ukena, Michael A Makara, Christopher T Sibley, Aimee D Shu
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Abstract

The PaTHway clinical trial demonstrated sustained efficacy, safety, and tolerability of daily palopegteriparatide in the treatment of adults with hypoparathyroidism. Palopegteriparatide treatment was also associated with improvements in estimated glomerular filtration rate (eGFR) over 52 wk in a post hoc analysis, prompting further exploration of palopegteriparatide in the preservation of renal function. The current post hoc analysis evaluated the impact of palopegteriparatide treatment on renal function in adults with hypoparathyroidism through Week 104; as with prior analysis, changes in renal function were assessed using eGFR. At Week 104, 93% (76/82) of participants remained in the open-label extension. Of those, 82% had albumin-adjusted serum calcium levels in the normal range (8.3-10.6 mg/dL), 97% were independent from conventional therapy (≤600 mg/d of elemental calcium and no active vitamin D). Mean (SD) serum phosphate (3.5 (0.7) mg/dL) and albumin-adjusted calcium × phosphate product (30.7(5.1) mg2/dL2) levels were also within normal ranges. Palopegteriparatide treatment resulted in a mean (SD) increase in eGFR of 8.9 (11.0) mL/min/1.73m2 (p < .0001) from baseline to Week 52, which was sustained through Week 104, where it was 77.8 (14.8) mL/min/1.73 m2 with a mean (SD) change from baseline of 9.0 (10.3) mL/min/1.73 m2 (p < .0001). By Week 104, 45% and 34% of participants had an increase in eGFR of ≥5 mL/min/1.73 m2 and ≥10 mL/min/1.73 m2, respectively. Palopegteriparatide treatment normalized mean (SD) 24-h urine calcium within 26 wk and maintained levels below 250 mg/d through Week 104 (158.8 (90.5) mg/24 h). Most treatment-emergent adverse events were mild or moderate; no new safety signals or cases of treatment-related nephrolithiasis were reported. These findings demonstrate sustained renal safety of palopegteriparatide and suggest that PTH replacement therapy with palopegteriparatide preserves and may improve renal function in adults with chronic hypoparathyroidism after 104 wk of treatment.

慢性甲状旁腺功能减退症成人患者使用Palopegteriparatide持续改善肾功能:来自3期通路试验的2年结果
PaTHway临床试验证明了每日使用palopegteriparatide治疗成人甲状旁腺功能减退的持续有效性、安全性和耐受性。在事后分析中,palopegteriparatite治疗也与52周的eGFR改善相关,这促使palopegteriparatite在肾功能保护方面的进一步探索。目前的事后分析评估了palopegteriparatide治疗对甲状旁腺功能低下成人患者104周肾功能的影响;与先前的分析一样,使用eGFR评估肾功能的变化。在第104周,93%(76/82)的参与者继续进行开放标签延长治疗。其中,82%的患者白蛋白调节的血清钙水平在正常范围内(8.3-10.6 mg/dL), 97%的患者独立于常规治疗(≤600 mg/天的单质钙和无活性维生素D)。平均(SD)血清磷酸盐(3.5 (0.7)mg/dL)和白蛋白调节的钙x磷酸产物(30.7(5.1)mg2/dL2)水平也在正常范围内。palopegteriparatite治疗导致eGFR平均(SD)增加8.9 (11.0)mL/min/1.73m2 (P
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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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