Department of Preventive Medicine and Public Health and the Landon Center on Aging, University of Kansas Medical Center, Kansas City, KS, USA.
Am J Kidney Dis. 2010 Dec;56(6):1108-16. doi: 10.1053/j.ajkd.2010.07.012. Epub 2010 Oct 15.
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.
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.
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 mg²/dL²) 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).
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.
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.
ACHIEVE(优化继发性甲状旁腺功能亢进症的治疗:西那卡塞联合低剂量活性维生素 D 类似物与单独使用高剂量维生素 D 类似物的比较)试验评估了西那卡塞联合低剂量活性维生素 D 类似物(Cinacalcet-D)与单独使用维生素 D 类似物(Flex-D)治疗继发性甲状旁腺功能亢进症(SHPT)的疗效,以达到 KDOQI(肾脏病预后质量倡议)的目标。这些治疗方案的经济意义尚未得到探讨。
血液透析患者继发性甲状旁腺功能亢进症治疗的经济分析。
本分析使用了 ACHIEVE 试验的数据,该试验中患者接受了 Cinacalcet-D 或 Flex-D 治疗。
模型、视角和时间范围:我们使用 2006 年的美国货币评估了美国支付者视角下这两种方案在 ACHIEVE 试验 27 周内治疗 SHPT 的相对成本效益,药物成本以药物成本衡量。干预和结果:使用成本最小化分析或增量成本效益比评估相对成本效益。有效性通过生化标志物测量。
Cinacalcet-D 和 Flex-D 治疗组的每位患者的平均药物成本分别为 5852 美元和 4332 美元。主要终点(甲状旁腺激素水平 150-300pg/mL 和钙磷乘积<55mg²/dL²)和一些次要终点无显著差异,Cinacalcet-D 比 Flex-D 更昂贵。对于 Cinacalcet-D 更有效的次要终点,每位患者达到目标的增量成本效益比从 2957 美元(钙<9.5mg/dL)到 22028 美元(所有 KDOQI 目标)不等。将骨化三醇转换为仿制药会增加治疗组之间的成本差异(2079 美元),而将司维拉姆转换为镧则会降低差异(1426 美元)。
成本和结果来自短期随机对照试验,并且是基于方案驱动的。没有可用的临床结果,如死亡率。不能从这些数据中得出长期的经济结论。
西那卡塞联合维生素 D 类似物在达到 ACHIEVE 的主要终点方面并不比维生素 D 类似物更有效,且成本更高。维生素 D 类似物或口服磷结合剂的成本并没有实质性地改变这一结论。西那卡塞的额外成本是否合理,需要通过更长期的模型来确定矿物质代谢标志物血清水平的变化是否会降低发病率、死亡率和下游成本。