Economic Analysis of Cinacalcet in Combination With Low-Dose Vitamin D Versus Flexible-Dose Vitamin D in Treating Secondary Hyperparathyroidism in Hemodialysis Patients

被引:20
作者
Shireman, Theresa I. [1 ,2 ]
Almehmi, Ammar [3 ]
Wetmore, James B. [4 ,5 ]
Lu, John [6 ,7 ]
Pregenzer, Mark [8 ]
Quarles, L. Darryl [9 ]
机构
[1] Univ Kansas, Med Ctr, Dept Prevent Med & Publ Hlth, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Landon Ctr Aging, Kansas City, KS 66160 USA
[3] Univ Arizona, Arizona Kidney Dis & Hypertens Ctr, Phoenix, AZ USA
[4] Univ Kansas, Med Ctr, Div Nephrol & Hypertens, Kansas City, KS 66160 USA
[5] Univ Kansas, Med Ctr, Kidney Inst, Kansas City, KS 66160 USA
[6] Outcomes Insights Inc, Channel Isl, England
[7] Calif State Univ, Channel Isl, England
[8] Ronald Reagan UCLA Med Ctr, Dept Pharmaceut Serv, Los Angeles, CA USA
[9] Univ Tennessee, Dept Med, Hlth Sci Ctr, Memphis, TN 38104 USA
关键词
End-stage renal disease; hemodialysis; secondary hyperparathyroidism; calcimimetics; vitamin D; cost-effectiveness; STAGE RENAL-DISEASE; CARDIOVASCULAR-DISEASE; CALCIMIMETIC AMG-073; PARATHYROID-HORMONE; MINERAL METABOLISM; COST-EFFECTIVENESS; DIALYSIS OUTCOMES; CALCITRIOL; CALCIUM; BONE;
D O I
10.1053/j.ajkd.2010.07.012
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: The ACHIEVE (Optimizing the Treatment of Secondary Hyperparathyroidism: A Comparison of Sensipar and Low Dose Vitamin D vs Escalating Doses of Vitamin D Alone) trial evaluated the efficacy of treatment with cinacalcet plus low-dose activated vitamin D analogues (Cinacalcet-D) compared with vitamin D analogues alone (Flex-D) in attaining KDOQI (Kidney Disease Outcomes Quality Initiative) targets for secondary hyperparathyroidism (SHPT). The economic implications of these treatment regimens have not been explored. Study Design: Economic analysis of SHPT treatment in hemodialysis patients. Setting & Population: This analysis used data from the ACHIEVE trial, in which patients received either Cinacalcet-D or Flex-D. Model, Perspective, & Time Frame: We assessed the relative cost-effectiveness of these regimens in treating SHPT during the 27-week ACHIEVE trial, using a US payer perspective, with medication costs valued in 2006 US dollars. Intervention & Outcomes: Relative cost-effectiveness was assessed using cost-minimization analysis or incremental cost-effectiveness ratios. Effectiveness was measured using biochemical markers. Results: Mean medication costs per patient were $5,852 and $4,332 for the Cinacalcet-D and Flex-D treatment arms, respectively. There were no significant differences for the primary end point (parathyroid hormone level of 150-300 pg/mL and calcium-phosphorus product < 55 mg(2)/dL(2)) and several of the secondary end points, rendering Cinacalcet-D more costly than Flex-D. For secondary end points, for which Cinacalcet-D was more effective, incremental cost-effectiveness ratios ranged from $2,957 (calcium < 9.5 mg/dL) to $22,028 (all KDOQI targets) per patient reaching target. Switching to generic calcitriol would have increased the cost difference between treatment arms ($2,079), whereas switching sevelamer to lanthanum decreased the difference ($1,426). Limitations: Costs and outcomes were derived from a short-term randomized controlled trial and were protocol driven. Clinical outcomes, such as mortality, were not available. Long-term economic conclusions cannot be drawn from these data. Conclusions: Cinacalcet combined with vitamin D analogues was no more effective than vitamin D analogues in achieving the primary ACHIEVE end point and incurred greater costs. This conclusion was not tempered substantially by the cost of vitamin D analogues or oral phosphate binders. Whether the additional costs of cinacalcet are warranted will require longer term models to determine whether changes in serum levels of mineral metabolic markers translate into lower morbidity, mortality, and downstream costs. Am J Kidney Dis 56: 1108-1116. (C) 2010 by the National Kidney Foundation, Inc.
引用
收藏
页码:1108 / 1116
页数:9
相关论文
共 30 条
[1]  
[Anonymous], 1996, COST EFFECTIVENESS H, DOI DOI 10.1093/OSO/9780195108248.001.0001
[2]  
Arenas MD, 2008, NEFROLOGIA, V28, P511
[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]   Effects of the calcimimetic cinacalcet HCl on cardiovascular disease, fracture, and health-related quality of life in secondary hyperparathyroidism [J].
Cunningham, J ;
Danese, M ;
Olson, K ;
Klassen, P ;
Chertow, GM .
KIDNEY INTERNATIONAL, 2005, 68 (04) :1793-1800
[6]   Consistent control of mineral and bone disorder in incident hemodialysis patients [J].
Danese, Mark D. ;
Belozeroff, Vasily ;
Smirnakis, Karen ;
Rothman, Kenneth J. .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2008, 3 (05) :1423-1429
[7]   PTH and the risks for hip, vertebral, and pelvic fractures among patients on dialysis [J].
Danese, MD ;
Kim, J ;
Doan, QV ;
Dylan, M ;
Griffiths, R ;
Chertow, GM .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2006, 47 (01) :149-156
[8]   Secondary hyperparathyroidism: Review of the disease and its treatment [J].
de Francisco, ALM .
CLINICAL THERAPEUTICS, 2004, 26 (12) :1976-1993
[9]   Implementation of 'K/DOQI Clinical Practice Guidelines for Bone Metabolism and Disease in Chronic Kidney Disease' after the introduction of cinacalcet in a population of patients on chronic haemodialysis [J].
Dolores Arenas, Maria ;
Alvarez-Ude, Fernando ;
Teresa Gil, Maria ;
Moledous, Analia ;
Malek, Tamara ;
Nunez, Carlos ;
Devesa, Ramon ;
Antonia Carreton, Maria ;
Soriano, Antonio .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2007, 22 (06) :1639-1644
[10]   On the evolving nature of understanding dialysis-related disorders [J].
Eknoyan, G ;
Lindberg, JS .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2003, 41 (04) :S1-S3