TY - JOUR
T1 - Comparison of the Oral Calcimimetics Evocalcet and Cinacalcet in East Asian Patients on Hemodialysis with Secondary Hyperparathyroidism
AU - Orchestra Study Group
AU - Ni, Zhaohui
AU - Liang, Xinling
AU - Wu, Chia Chao
AU - Jin, Kyubok
AU - Kim, Yong Lim
AU - Lu, Kuo Cheng
AU - Chan, Tak Mao
AU - Fukagawa, Masafumi
AU - Kinoshita, Jun
AU - Nagai, Chisato
AU - Kojima, Masahiro
AU - Yu, Xueqing
AU - Xinling, Liang
AU - Shuangxin, Liu
AU - Sijia, Li
AU - Lixia, Xu
AU - Zhiming, Ye
AU - Zhonglin, Feng
AU - Renwei, Huang
AU - Zhilian, Li
AU - Wei, Chen
AU - Xunhua, Zheng
AU - Naya, Huang
AU - Zhen, Ai
AU - Xin, Wang
AU - former PI, PI
AU - present PI, PI
AU - Renhua, Lu
AU - Jianxiao, Shen
AU - Yijun, Zhou
AU - Xinghui, Lin
AU - Yuanyuan, Xie
AU - Jiahui, Zhang
AU - Miaolin, Che
AU - Yan, Fang
AU - Huihua, Pang
AU - Xinyu, Su
AU - Leyi, Gu
AU - Wei, Jin
AU - Peipei, Zhao
AU - Yiwei, Shen
AU - Liou, Zao
AU - Wei, Lu
AU - Haidong, Huang
AU - Gang, Ji
AU - Hao, Li
AU - Deguang, Wang
AU - Liang, Yuan
AU - Tarng, Der Cherng
AU - Chou, Kang Ju
N1 - Publisher Copyright:
© 2023
PY - 2023/11
Y1 - 2023/11
N2 - Introduction: Evocalcet is an oral calcimimetic agent with proven efficacy and safety in treating secondary hyperparathyroidism (SHPT) in Japanese patients on dialysis. Methods: This randomized, double-blind, intrapatient dose-adjustment, parallel-group, international multicenter study compared the efficacy and safety of evocalcet versus cinacalcet for 52 weeks in East Asian hemodialysis patients with SHPT. Results: In total, 203 and 200 patients were randomized to receive evocalcet or cinacalcet, respectively (overall, 70.1% had baseline intact parathyroid hormone (PTH) levels ≥500 pg/ml, with no between-group difference). Mean percentage changes in intact PTH levels from baseline were −34.7% and −30.2% in the evocalcet and cinacalcet groups at 52 weeks (between-group difference −4.4%, 95% confidence interval [CI] −13.1%, 4.3%, below the predefined 15% noninferiority margin). Overall, 67.3% and 58.7% of patients in the evocalcet and cinacalcet groups, respectively, achieved ≥30% decrease in intact PTH levels from baseline (between-group difference 8.6%; 95% CI −1.8%, 19.1%). No major safety concerns were observed. Gastrointestinal adverse events (AEs) were significantly less frequent with evocalcet compared with cinacalcet (33.5% vs. 50.5%, P = 0.001), whereas the incidence of hypocalcemia did not differ. Conclusion: Evocalcet might be a better alternative to cinacalcet for East Asian patients on hemodialysis with SHPT.
AB - Introduction: Evocalcet is an oral calcimimetic agent with proven efficacy and safety in treating secondary hyperparathyroidism (SHPT) in Japanese patients on dialysis. Methods: This randomized, double-blind, intrapatient dose-adjustment, parallel-group, international multicenter study compared the efficacy and safety of evocalcet versus cinacalcet for 52 weeks in East Asian hemodialysis patients with SHPT. Results: In total, 203 and 200 patients were randomized to receive evocalcet or cinacalcet, respectively (overall, 70.1% had baseline intact parathyroid hormone (PTH) levels ≥500 pg/ml, with no between-group difference). Mean percentage changes in intact PTH levels from baseline were −34.7% and −30.2% in the evocalcet and cinacalcet groups at 52 weeks (between-group difference −4.4%, 95% confidence interval [CI] −13.1%, 4.3%, below the predefined 15% noninferiority margin). Overall, 67.3% and 58.7% of patients in the evocalcet and cinacalcet groups, respectively, achieved ≥30% decrease in intact PTH levels from baseline (between-group difference 8.6%; 95% CI −1.8%, 19.1%). No major safety concerns were observed. Gastrointestinal adverse events (AEs) were significantly less frequent with evocalcet compared with cinacalcet (33.5% vs. 50.5%, P = 0.001), whereas the incidence of hypocalcemia did not differ. Conclusion: Evocalcet might be a better alternative to cinacalcet for East Asian patients on hemodialysis with SHPT.
KW - East Asia
KW - cinacalcet
KW - evocalcet
KW - gastrointestinal
KW - randomized controlled trial
KW - secondary hyperparathyroidism
UR - http://www.scopus.com/inward/record.url?scp=85171549638&partnerID=8YFLogxK
U2 - 10.1016/j.ekir.2023.08.034
DO - 10.1016/j.ekir.2023.08.034
M3 - Article
AN - SCOPUS:85171549638
SN - 2468-0249
VL - 8
SP - 2294
EP - 2306
JO - Kidney International Reports
JF - Kidney International Reports
IS - 11
ER -