Cost-Effectiveness Analysis of Peginterferon Beta-1a in the Treatment of Relapsing-Remitting Multiple Sclerosis in Italy: Results of an Updated Analysis
IF 0.4
Q4 HEALTH CARE SCIENCES & SERVICES
D. Centonze, S. Iannazzo, L. Santoni, C. Saleri, E. Puma, L. Giuliani, P. Canonico
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Abstract
© 2018 The Authors. Published by SEEd srl. This is an open access article under the CC BY-NC 4.0 license (https://creativecommons.org/licenses/by-nc/4.0) background Multiple sclerosis (MS), a chronic inflammatory disease of the central nervous system, is causing a progressive disability that impacts patients’ quality of life and societal costs [1]. MS takes several forms, with new symptoms either occurring in isolated attacks (relapsing form) or building up over time (progressive form) [2]. Between attacks, symptoms may disappear completely; however, permanent neurological problems often remain, especially as the disease advances [2]. In 85% of patients with MS the onset form is relapsing-remitting MS (RRMS) [3]. While MS is currently considered incurable, treatment has advanced significantly over the past several decades. Disease modifying therapies (DMTs) can reduce the frequency of clinical relapses and delay disability progression [4]. As is the case in many different therapeutic areas, clinical progress in treating the disease has accompanied a rise in costs to purchase biologic products. In this light, economic evaluations are key elements for healthcare decision-making. In 2016 we published in this journal a cost-effectiveness analysis that compared subcutaneous peginterferon beta-1a 125 μg every 2 weeks (Plegridy®) to the other injectable DMTs used in first-line therapy of RRMS from both the perspective of the Italian National Healthcare Service (NHS) and of the Italian Society [5]. The comparators considered in the analysis were: interferon (IFN) beta-1a 30 μg (Avonex®), IFN beta-1a 22 μg (Rebif® 22), IFN beta-1a 44 μg (Rebif® 44), glatiramer acetate (GA, Copaxone®) 20 mg, IFN beta-1b 250 μg (Betaferon® and Extavia®). The 2016 analysis showed that peginterferon beta-1a was an alternative dominant or cost-effective vs IFNs and GA for the treatment of RRMS in Italy from the NHS and societal perspectives. While the design of the model and the choice of clinical parameters remains well aligned with the most recent cost-effectiveness studies published in the literature [6], some economic inputs of that analysis appear now outdated. The objective of the current work is thus to provide an update of the original analysis [5]. Corresponding author Prof. Diego Centonze centonze@uniroma2.it
聚乙二醇干扰素β -1a治疗意大利复发缓解型多发性硬化症的成本-效果分析:最新分析结果
©2018作者。由SEEd出版社出版。多发性硬化症(MS)是一种中枢神经系统的慢性炎症性疾病,导致进行性残疾,影响患者的生活质量和社会成本[1]。多发性硬化症有多种表现形式,新的症状要么在孤立发作时出现(复发型),要么随着时间的推移逐渐积累(进行性)[2]。在两次发作之间,症状可能完全消失;然而,永久性的神经问题往往仍然存在,特别是随着疾病的进展[2]。85%的MS患者发病形式为复发缓解型MS (RRMS)[3]。虽然多发性硬化症目前被认为是无法治愈的,但在过去的几十年里,治疗已经取得了重大进展。疾病修饰疗法(dmt)可以减少临床复发的频率,延缓残疾进展[4]。与许多不同治疗领域的情况一样,治疗该病的临床进展伴随着购买生物制品的成本上升。在这种情况下,经济评估是医疗保健决策的关键因素。2016年,我们在该杂志上发表了一项成本效益分析,从意大利国家医疗保健服务(NHS)和意大利社会的角度比较了每2周125 μg皮下聚乙二醇干扰素β -1a (Plegridy®)与用于RRMS一线治疗的其他注射DMTs的成本效益分析[5]。分析中考虑的比较物为:干扰素(IFN) β -1a 30 μg (Avonex®)、IFN β -1a 22 μg (Rebif®22)、IFN β -1a 44 μg (Rebif®44)、醋酸格拉替雷明(GA、Copaxone®)20 mg、IFN β -1b 250 μg (Betaferon®和Extavia®)。2016年的分析显示,从NHS和社会的角度来看,聚乙二醇干扰素β -1a是意大利治疗RRMS的替代优势或成本效益优于ifn和GA。虽然模型的设计和临床参数的选择与文献中发表的最新成本效益研究保持一致[6],但该分析的一些经济投入现在似乎过时了。因此,当前工作的目的是提供原始分析的更新[5]。通讯作者Diego Centonze教授centonze@uniroma2.it
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