Department of Medicine, University of Rochester Medical Center, 601 Elmwood Ave, Box 648, Rochester, NY 14642, USA.
Pharmacoeconomics. 2013 Jun;31(6):455-69. doi: 10.1007/s40273-013-0063-4.
Several cost-effectiveness models of disease-modifying treatments (DMTs) for multiple sclerosis (MS) have been developed for different populations and different countries. Vast differences in the approaches and discrepancies in the results give rise to heated discussions and limit the use of these models. Our main objective is to discuss the methodological challenges in modelling the cost effectiveness of treatments for MS. We conducted a review of published models to describe the approaches taken to date, to identify the key parameters that influence the cost effectiveness of DMTs, and to point out major areas of weakness and uncertainty. Thirty-six published models and analyses were identified. The greatest source of uncertainty is the absence of head-to-head randomized clinical trials. Modellers have used various techniques to compensate, including utilizing extension trials. The use of large observational cohorts in recent studies aids in identifying population-based, 'real-world' treatment effects. Major drivers of results include the time horizon modelled and DMT acquisition costs. Model endpoints must target either policy makers (using cost-utility analysis) or clinicians (conducting cost-effectiveness analyses). Lastly, the cost effectiveness of DMTs outside North America and Europe is currently unknown, with the lack of country-specific data as the major limiting factor. We suggest that limited data should not preclude analyses, as models may be built and updated in the future as data become available. Disclosure of modelling methods and assumptions could improve the transferability and applicability of models designed to reflect different healthcare systems.
已经为不同人群和国家开发了几种多发性硬化症(MS)的疾病修正治疗(DMT)的成本效益模型。这些模型在方法上存在巨大差异,结果也存在差异,这引发了激烈的讨论,并限制了这些模型的使用。我们的主要目标是讨论 MS 治疗成本效益建模中的方法学挑战。我们对已发表的模型进行了综述,以描述迄今为止采用的方法,确定影响 DMT 成本效益的关键参数,并指出主要的弱点和不确定性领域。确定了 36 个已发表的模型和分析。最大的不确定性来源是缺乏头对头的随机临床试验。建模者使用了各种技术来进行补偿,包括利用扩展试验。最近的研究中使用大型观察性队列有助于确定基于人群的“真实世界”治疗效果。结果的主要驱动因素包括所建模的时间范围和 DMT 获得成本。模型终点必须针对决策者(使用成本效用分析)或临床医生(进行成本效益分析)。最后,目前尚不清楚北美和欧洲以外地区 DMT 的成本效益,缺乏特定国家的数据是主要的限制因素。我们建议,由于缺乏数据,不应排除分析,因为随着数据的可用,未来可能会构建和更新模型。披露建模方法和假设可以提高为反映不同医疗保健系统而设计的模型的可转移性和适用性。