Romero Martín, Chávez Diana, De Los Ríos Magalí, Alvis-Guzmán Nelson
Fundación Salutia, Centro de Investigaciones en Economía, Gestión y Tecnologías en Salud, Bogotá, D.C., Colombia.
External Advisory Consultant in Hematology, Bogotá, D.C., Colombia.
Biomedica. 2014 Jan-Mar;34(1):48-59. doi: 10.1590/S0120-41572014000100008.
New tyrosine kinase inhibitor treatments for chronic myeloid leukemia based on nilotinib, dasatinib and imatinib have improved patient quality of life and have turned chronic myeloid leukemia from a fatal disease into a chronic disease.
To evaluate the cost-effectiveness of nilotinib, 600 mg, and dasatinib, 100 mg, each compared to imatinib, 400 mg, as first-line therapy in chronic myeloid leukemia in Colombia from a third-party payer's perspective.
A cost-effectiveness analysis was performed using a Markov model to evaluate a hypothetical cohort of one hundred 55 year-old patients with newly diagnosed chronic myeloid leukemia in the chronic phase, and the time horizon for the baseline case was established as being until the end of life. Progression-free life-years saved were considered the primary outcome. Transition probabilities for major molecular response, disease progression to accelerated phase or blast crisis, and chronic myeloid leukemia related deaths were analyzed in the model for each arm. A 3% discount rate was applied to all costs and patient outcomes. Model robustness was evaluated using both univariate and multivariate Montecarlo sensitivity analysis.
Nilotinib was higher in expected progression-free life-years saved (15.21 vs. 12.64 for imatinib), followed by dasatinib (14.91 vs. 14.54 for imatinib). Imatinib had lower total lifetime costs. The incremental cost-effectiveness ratio was US$ 33,120.36 in the nilotinib arm and US$ 514,939.08 in the dasatinib arm per progression-free life-years (PF-LYs) saved, each compared to imatinib. When analyzing nilotinib versus dasatinib indirectly, nilotinib was found to be dominant due to higher efficacy (2.25 PF-LYs) and lower costs (US$ 44,674) in the baseline case. The average estimated cost to manage disease progression per year was US$ 101,978.78, considered to be the threshold.
In Colombia, using PF-LYs as the efficacy outcome, nilotinib is highly cost-effective when compared to imatinib and dominant vs. dasatinib in first-line therapy for CML in chronic phase.
基于尼洛替尼、达沙替尼和伊马替尼的慢性髓性白血病新型酪氨酸激酶抑制剂治疗改善了患者的生活质量,并将慢性髓性白血病从一种致命疾病转变为一种慢性疾病。
从第三方支付方的角度评估在哥伦比亚,与400毫克伊马替尼相比,600毫克尼洛替尼和100毫克达沙替尼作为慢性髓性白血病一线治疗药物的成本效益。
使用马尔可夫模型进行成本效益分析,以评估一组假设的100名55岁新诊断为慢性期慢性髓性白血病患者,基线病例的时间范围设定为直至生命结束。无进展生存年数的增加被视为主要结局。在模型中分析了每个治疗组达到主要分子反应、疾病进展至加速期或急变期以及慢性髓性白血病相关死亡的转移概率。所有成本和患者结局均采用3%的贴现率。使用单变量和多变量蒙特卡洛敏感性分析评估模型的稳健性。
尼洛替尼在预期无进展生存年数的增加方面更高(与伊马替尼相比为15.21对12.64),其次是达沙替尼(与伊马替尼相比为14.91对14.54)。伊马替尼的终身总成本较低。与伊马替尼相比,尼洛替尼组每增加一个无进展生存年数(PF-LYs)的增量成本效益比为33,120.36美元,达沙替尼组为514,939.08美元。在间接比较尼洛替尼和达沙替尼时,发现尼洛替尼具有优势,因为在基线病例中其疗效更高(2.25个PF-LYs)且成本更低(44,674美元)。每年管理疾病进展的平均估计成本为101,978.78美元,被视为阈值。
在哥伦比亚,以PF-LYs作为疗效结局,与伊马替尼相比,尼洛替尼在慢性期慢性髓性白血病一线治疗中具有很高的成本效益,且相对于达沙替尼具有优势。