Cinacalcet hydrochloride is an effective treatment for secondary hyperparathyroidism in patients with CKD not receiving dialysis

被引:101
作者
Charytan, C
Coburn, JW
Chonchol, M
Herman, J
Lien, YH
Liu, W
Klassen, PS
McCary, LC
Pichette, V
机构
[1] New York Hosp, Queens Med Ctr, Flushing, NY 11355 USA
[2] Vet Affairs Greater Los Angeles Hlth Care Serv, Los Angeles, CA USA
[3] Univ Colorado, Denver, CO 80202 USA
[4] Palmetto Internal Med, Columbia, SC USA
[5] Univ Arizona, Tucson, AZ USA
[6] Amgen Inc, Thousand Oaks, CA 91320 USA
[7] Hop Maison Neuve Rosemont, Montreal, PQ H1T 2M4, Canada
关键词
calcimimetic; chronic kidney disease (CKD); hyperparathyroidism; predialysis;
D O I
10.1053/j.ajkd.2005.04.013
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. Secondary hyperparathyroidism develops early in patients with chronic kidney disease (CKD). Clinical guidelines from the National Kidney Foundation-Kidney/Disease Outcomes Quality Initiative emphasize the need to control parathyroid hormone (PTH), calcium, and phosphorus levels in patients with CKD not receiving dialysis to reduce poor outcomes. This phase 2 study evaluated the effects of the oral calcimimetic cinacalcet hydrochloride in patients with CKD not on dialysis therapy. Methods: A randomized, double-blind, placebo-controlled, 18-week study enrolled adults with an estimated glomerular filtration rate of 15 to 50 mL/min/1.73 m(2) (0.25 to 0.83 mL/s/1.73 m(2)) and an intact PTH (iPTH) level greater than 130 pg/mL (ng/L). Cinacalcet (or placebo) was titrated from 30 to 180 mg once daily to obtain a 30% or greater reduction in iPTH levels from baseline. Results: Baseline mean iPTH levels were 243 pg/mL (ng/L) in the cinacalcet group (n = 27) and 236 pg/mL (ng/L) in the control group (n = 27). At baseline, 28% of subjects were being administered vitamin D sterols and 43% were being administered phosphate binders or calcium supplements. The addition of cinacalcet significantly decreased iPTH concentrations compared with controls during the efficacy-assessment phase: 56% versus 19% of subjects achieved a 30% or greater reduction in iPTH levels (P = 0.006), and mean iPTH levels decreased by 32% in the cinacalcet group, but increased by 6% in the control group (P < 0.001). Mean serum calcium and phosphorus levels remained within normal range throughout the study. Cinacalcet generally was well tolerated; the most frequent adverse events were gastrointestinal. Conclusion: This preliminary study provides evidence that cinacalcet is efficacious for the treatment of secondary hyperparathyroidism in subjects with CKD not receiving dialysis. (c) 2005 by the National Kidney Foundation, Inc.
引用
收藏
页码:58 / 67
页数:10
相关论文
共 38 条
[1]  
BLOCK G, 2004, HEMODIAL INT, V8, P265
[2]   Cinacalcet for secondary hyperparathyroidism in patients receiving hemodialysis [J].
Block, GA ;
Martin, KJ ;
de Francisco, ALM ;
Turner, SA ;
Avram, MM ;
Suranyi, MG ;
Hercz, G ;
Cunningham, J ;
Abu-Alfa, AK ;
Messa, P ;
Coyne, DW ;
Locatelli, F ;
Cohen, RM ;
Evenepoel, P ;
Moe, SM ;
Fournier, A ;
Braun, J ;
McCary, LC ;
Zani, VJ ;
Olson, KA ;
Drüeke, TB ;
Goodman, WG .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (15) :1516-1525
[3]   Mineral metabolism, mortality, and morbidity in maintenance hemodialysis [J].
Block, GA ;
Klassen, PS ;
Lazarus, JM ;
Ofsthun, N ;
Lowrie, EG ;
Chertow, GM .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (08) :2208-2218
[4]   Association of serum phosphorus and calcium x phosphate product with mortality risk in chronic hemodialysis patients: A national study [J].
Block, GA ;
Hulbert-Shearon, TE ;
Levin, NW ;
Port, FK .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (04) :607-617
[5]   Extracellular calcium sensing and extracellular calcium signaling [J].
Brown, EM ;
MacLeod, RJ .
PHYSIOLOGICAL REVIEWS, 2001, 81 (01) :239-297
[6]  
Chonchol M, 2004, AM J KIDNEY DIS, V43, pA19
[7]   Renal bone disease in 76 patients with varying degrees of predialysis chronic renal failure: A cross-sectional study [J].
Coen, G ;
Mazzaferro, S ;
Ballanti, P ;
Sardella, D ;
Chicca, S ;
Manni, M ;
Bonucci, E .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1996, 11 (05) :813-819
[8]   WHO GETS RENAL BONE-DISEASE BEFORE BEGINNING DIALYSIS [J].
CUNDY, T ;
HAND, DJ ;
OLIVER, DO ;
WOODS, CG ;
WRIGHT, FW ;
KANIS, JA .
BRITISH MEDICAL JOURNAL, 1985, 290 (6464) :271-275
[9]   The severity of secondary hyperparathyroidism in chronic renal insufficiency is GFR-dependent, race-dependent, and associated with cardiovascular disease [J].
De Boer, IH ;
Gorodetskaya, I ;
Young, B ;
Hsu, CY ;
Chertow, GM .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2002, 13 (11) :2762-2769
[10]   THE PATHOGENESIS OF PARATHYROID-GLAND HYPERPLASIA IN CHRONIC-RENAL-FAILURE [J].
DRUEKE, TB .
KIDNEY INTERNATIONAL, 1995, 48 (01) :259-272