van den Akker-van Marle M Elske, Gurwitz David, Detmar Symone B, Enzing Christine M, Hopkins Michael M, Gutierrez de Mesa Emma, Ibarreta Dolores
TNO (Netherlands Organization for Applied Scientific Research), Quality of Life, Leiden/Delft, The Netherlands.
Pharmacogenomics. 2006 Jul;7(5):783-92. doi: 10.2217/14622416.7.5.783.
Only a few studies have addressed the cost-effectiveness of pharmacogenetics interventions in healthcare. Lack of health economics data on aspects of pharmacogenetics is perceived as one of the barriers hindering its implementation for improving drug safety. Thus, a recent Institute for Prospective Technological Studies (IPTS) study, entitled 'Pharmacogenetics and pharmacogenomics: state-of-the-art and potential socio-economic impact in the EU' included an explorative cost-effectiveness review for a pharmacogenetic treatment strategy compared with traditional medical practice. The selected case study examined the cost-effectiveness of thiopurine methyltransferase (TMPT) genotyping prior to thiopurine treatment in children with acute lymphoblastic leukemia (ALL). Information for the cost-effectiveness model parameters was collected from literature surveys and interviews with experts from four European countries (Germany, Ireland, the Netherlands and the UK). The model has established that TPMT testing in ALL patients has a favorable cost-effectiveness ratio. This conclusion was based on parameters collected for TPMT genotyping costs, estimates for frequency of TMPT deficiency, rates of thiopurine-mediated myelosuppression in TPMT-deficient individuals, and myelosuppression-related hospitalization costs in each of the four countries studied. The mean calculated cost per life-year gained by TPMT genotyping in ALL patients in the four study countries was euro 2100 (or euro 4800 after 3% discount) based on genotyping costs of euro 150 per patient. Cost per life-year gained is expected to further improve following the introduction of the wider use of TMPT genotyping and the availability of lower cost genotyping methods. Our analysis indicates that TPMT genotyping should be seriously considered as an integral part of healthcare prior to the initiation of therapy with thiopurine drugs.
仅有少数研究探讨了药物遗传学干预措施在医疗保健中的成本效益。缺乏关于药物遗传学方面的卫生经济学数据被视为阻碍其用于改善药物安全性的障碍之一。因此,近期未来技术研究协会(IPTS)开展了一项题为“药物遗传学和药物基因组学:欧盟的现状及潜在社会经济影响”的研究,其中包括一项探索性成本效益评估,将一种药物遗传学治疗策略与传统医疗实践进行比较。所选案例研究考察了在儿童急性淋巴细胞白血病(ALL)患者中,硫嘌呤治疗前进行硫嘌呤甲基转移酶(TMPT)基因分型的成本效益。成本效益模型参数的信息是通过文献调查以及与来自四个欧洲国家(德国、爱尔兰、荷兰和英国)的专家访谈收集的。该模型已证实,对ALL患者进行TPMT检测具有良好的成本效益比。这一结论是基于为TPMT基因分型成本收集的参数、TMPT缺乏症的频率估计、TPMT缺乏个体中硫嘌呤介导的骨髓抑制发生率,以及在所研究的四个国家中与骨髓抑制相关的住院费用得出的。基于每位患者150欧元的基因分型成本,在四个研究国家中,ALL患者通过TPMT基因分型每获得一个生命年的平均计算成本为2100欧元(3%贴现后为4800欧元)。随着TPMT基因分型的更广泛应用以及低成本基因分型方法的出现,预计每获得一个生命年的成本将进一步降低。我们的分析表明,在开始使用硫嘌呤类药物治疗之前,应认真考虑将TPMT基因分型作为医疗保健的一个组成部分。