Effect of tolvaptan in Japanese patients with autosomal dominant polycystic kidney disease: a post hoc analysis of TEMPO 3:4 and TEMPO Extension Japan

被引:6
|
作者
Muto, Satoru [1 ,2 ]
Okada, Tadashi [3 ]
Shibasaki, Yoshiyuki [4 ]
Ibuki, Tatsuki [4 ]
Horie, Shigeo [1 ,2 ]
机构
[1] Juntendo Univ, Grad Sch Med, Dept Adv Informat Genet Dis, Bunkyo Ku, Hongo 2-1-1, Tokyo 1138421, Japan
[2] Juntendo Univ, Sch Med, Dept Urol, Bunkyo Ku, Hongo 2-1-1, Tokyo 1138421, Japan
[3] Otsuka Pharmaceut Co Ltd, Dept Clin Dev, Osaka, Japan
[4] Otsuka Pharmaceut Co Ltd, Med Affairs, Tokyo, Japan
关键词
Tolvaptan; Autosomal dominant polycystic kidney disease (ADPKD); Estimated glomerular filtration rate (eGFR); Total kidney volume (TKV); TEMPO; 3; 4; TEMPO Extension Japan (TEMPO-EXTJ);
D O I
10.1007/s10157-021-02083-y
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Autosomal dominant polycystic kidney disease (ADPKD) is a progressive condition that eventually leads to end-stage renal disease. A phase 3 trial of tolvaptan (TEMPO 3:4; NCT00428948) and its open-label extension (TEMPO Extension Japan: TEMPO-EXTJ; NCT01280721) were conducted in patients with ADPKD. In this post hoc analysis, effects on renal function and the safety profile of tolvaptan were assessed over a long-term period that included the 3-year TEMPO 3:4 and the approximately 3-year TEMPO-EXTJ trials. Methods Patients from Japanese trial sites who completed TEMPO 3:4 were offered participation in TEMPO-EXTJ. Patients whose efficacy parameters were measured at year 2 in TEMPO-EXTJ for efficacy evaluation were included. The annual slope of the estimated glomerular filtration rate (eGFR) and growth in total kidney volume (TKV) were analyzed. Results In patients who received tolvaptan in TEMPO 3:4 and TEMPO-EXTJ, the annual slope of eGFR (mL/min/1.73 m(2)) was - 3.480 in TEMPO 3:4 and - 3.417 in TEMPO-EXTJ, with no apparent effect of an approximately 3.6-month off-treatment interval between the two trials. In patients who received a placebo in TEMPO 3:4 before initiating tolvaptan in TEMPO-EXTJ, the slope of eGFR was significantly less steep from TEMPO 3:4 (- 4.287) to TEMPO-EXTJ (- 3.364), a difference of 0.923 (P = 0.0441). Conclusion The TEMPO-EXTJ trial supports a sustained beneficial effect of tolvaptan on eGFR. In patients who received a placebo in TEMPO 3:4, initiation of tolvaptan in TEMPO-EXTJ was associated with a significant slowing of eGFR decline.
引用
收藏
页码:1003 / 1010
页数:8
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