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治疗药物监测在慢性髓性白血病基于药物治疗中的成本效益。

The cost-effectiveness of therapeutic drug monitoring for the prescription drug-based treatment of chronic myeloid leukemia.

机构信息

Boston University, Questrom School of Business, Department of Markets, Public Policy, and Law, Boston, MA.

University of South Carolina, School of Pharmacy, Department of Pharmaceutical & Health Economics, Los Angeles, CA.

出版信息

J Manag Care Spec Pharm. 2021 Aug;27(8):1077-1085. doi: 10.18553/jmcp.2021.27.8.1077.

Abstract

A recent study demonstrating the use of Therapeutic Drug Monitoring (TDM) in patients with chronic myeloid leukemia (CML) resulted in a higher response rate with imatinib (IM) than demonstrated in second-generation tyrosine kinase inhibitor studies. The cost-effectiveness of TDM combined with IM (IM TDM) in first-line CML treatment has not yet been studied. To determine the cost-effectiveness of IM TDM for the first-line treatment of CML compared to tyrosine kinase inhibitor only treatment. A recently published cost-effectiveness model of tyrosine kinase inhibitor-treatment in CML was modified to include IM TDM as a first-line tyrosine kinase inhibitor-based CML treatment option. Efficacy inputs for major molecular response (MMR) rates were taken from previously published studies: IM TDM 65%, dasatinib 52%, nilotinib 53%. Annual tyrosine kinase inhibitor drug prices were derived from the Federal Supply Schedule (FSS) and the average and lowest wholesale acquisition costs (WAC) reported in the Red Book; the annual cost of TDM was $228. Other input costs modeled in the original CML CEA model were updated to 2016 US dollars using the medical service component of the Consumer Price Index. A US payer perspective was used with a 5-year time horizon and a 3.0% discount rate. The model compared first-line IM TDM versus IM alone, nilotinib (NIL) or dasatinib (DAS) in terms of the following outcomes: costs, quality-adjusted life-years (QALYs), and cost-effectiveness (total cost/QALY). Deterministic and probabilistic sensitivity analyses were performed using all key clinical and economic parameters. This study found that IM TDM dominates IM alone with $15,452 to $36,940 in savings and 0.25 higher QALYs. Using FSS, per patient total costs for IM and IM TDM were $270,905 and $233,965, respectively.; Using average WAC, these costs were $461,657 and $446,205, and using lowest WAC, these costs were $366,966 and $350,090. The results comparing first line using of IM TDM to NIL/DAS found that TDM IM had higher QALYs and lower costs (0.08 QALYs lower, and $117,006 to $172,420 savings per patient [varying by price basis]). Thus, in terms of cost-effectiveness, IM TDM dominates NIL/DAS with both lower costs and higher QALYs. IM TDM is a clinically and economically viable first-line treatment option for CML. This study was funded by Saladax Biomedical. Salamone is an employee of Saladax Biomedical. This study was presented at the IATDMCT Congress, September 2018, Brisbane, Australia.

摘要

最近的一项研究表明,在慢性髓性白血病(CML)患者中使用治疗药物监测(TDM)可使伊马替尼(IM)的反应率高于第二代酪氨酸激酶抑制剂研究中的反应率。在 CML 的一线治疗中,尚未研究 TDM 联合 IM(IM TDM)的成本效益。目的是确定与仅用酪氨酸激酶抑制剂治疗相比,IM TDM 在 CML 的一线治疗中的成本效益。对 CML 中酪氨酸激酶抑制剂治疗的最近发表的成本效益模型进行了修改,以将 IM TDM 作为一线基于酪氨酸激酶抑制剂的 CML 治疗选择纳入其中。主要分子反应(MMR)率的疗效输入来自先前发表的研究:IM TDM 为 65%,达沙替尼为 52%,尼洛替尼为 53%。每年酪氨酸激酶抑制剂药物价格来自联邦供应时间表(FSS)和 Red Book 中报告的平均和最低批发收购成本(WAC);TDM 的年成本为 228 美元。在原始 CML CEA 模型中建模的其他投入成本已使用消费者价格指数的医疗服务部分更新为 2016 年的美元。使用美国付款人观点,时间范围为 5 年,贴现率为 3.0%。该模型根据以下结果比较了一线 IM TDM 与 IM 单独、尼洛替尼(NIL)或达沙替尼(DAS):成本、质量调整生命年(QALYs)和成本效益(总成本/QALY)。使用所有关键临床和经济参数进行了确定性和概率敏感性分析。这项研究发现,IM TDM 优于 IM 单独使用,节省了 15452 至 36940 美元,QALY 提高了 0.25。使用 FSS,IM 和 IM TDM 的每位患者总费用分别为 270905 美元和 233965 美元;使用平均 WAC,这些成本分别为 461657 美元和 446205 美元,使用最低 WAC,这些成本分别为 366966 美元和 350090 美元。将一线使用 IM TDM 与 NIL/DAS 进行比较的结果发现,TDM IM 具有更高的 QALYs 和更低的成本(每个患者低 0.08 QALYs,节省 117006 至 172420 美元[取决于价格基础])。因此,就成本效益而言,IM TDM 优于 NIL/DAS,具有更低的成本和更高的 QALYs。IM TDM 是 CML 的一种具有临床和经济可行性的一线治疗选择。本研究由 Saladax Biomedical 资助。萨拉蒙是 Saladax Biomedical 的员工。这项研究在 2018 年 9 月澳大利亚布里斯班举行的 IATDMCT 大会上进行了介绍。

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