The value of the reflective discussion in decision-making using multi-criteria decision analysis (MCDA): an example of determining the value contribution of tabelecleucel for the treatment of the Epstein Barr virus-positive post-transplant lymphoproliferative disease (EBV+ PTLD).

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Xavier Badia, Miguel Ángel Calleja, Vicente Escudero-Vilaplana, Antonio Pérez-Martínez, José Luis Piñana, José Luis Poveda, Joan-Antoni Vallès
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引用次数: 0

Abstract

Background: The aim of this study was to assess the contribution of the reflective multidisciplinary discussion in determining the value contribution of innovative drugs through the multi-criteria decision analysis (MCDA). This methodology considers all relevant criteria for healthcare decision-making in a global, transparent, and systematic manner and from the perspective of relevant stakeholders. The determination of value contribution of tabelecleucel for the treatment of Epstein-Barr virus-positive post-transplant lymphoproliferative disease (EBV+ PTLD) compared to salvage therapy was used as an example.

Results: Tabelecleucel obtained a value contribution score of 0.63 and increased to 0.75 after the reflective discussion. EBV+ PTLD was considered a life-threatening disease (5.0 ± 0.0), with a significant unmet need for an approved treatment (5.0 ± 0.0). Tabelecleucel was perceived as bringing improvements in terms of efficacy (4.2 ± 0.8) and safety (3.8 ± 0.8) compared to the salvage therapy. Most experts considered that the high efficacy and safety results could represent an improvement in the quality of life of patients (2.3 ± 1.2) along with savings in medical costs (2.3 ± 2.0) and non-medical costs (2.7 ± 1.6) compared to the salvage therapy. However, others emphasized the need of more evidence to confirm these improvements and savings over time. Tabelecleucel was regarded as potentially modifying the clinical course of the disease (4.3 ± 0.8) and supported by high-quality evidence (3.2 ± 0.4). All contextual criteria were valued highly positively for tabelecleucel. "Safety/Tolerability" and "Other medical costs" were the criteria that experienced the highest change in the re-test conducted after the reflective discussion. The reflective discussion allowed resolving doubts or misinterpretations of the experts, so the re-test obtained more accurate and consistent results of the value contribution of tabelecleucel.

Conclusions: The study shows that the MCDA methodology is a useful tool for decision-making on innovative treatments for the management of rare diseases. It also highlights the importance of reflective multidisciplinary discussion for its ability to resolve doubts or misinterpretations of experts, subsequently allowing to obtain more consistent and reliable results on the value contribution of the drug, being potentially more positive.

使用多标准决策分析(MCDA)进行反思性讨论在决策中的价值:以确定Tabelecleucel治疗EB病毒阳性移植后淋巴组织增生性疾病(EBV+ PTLD)的价值贡献为例。
研究背景本研究旨在通过多标准决策分析(MCDA)评估多学科反思性讨论在确定创新药物价值贡献方面的贡献。该方法以全面、透明、系统的方式,从相关利益方的角度出发,考虑了医疗决策的所有相关标准。以确定Tabelecleucel治疗EB病毒阳性移植后淋巴组织增生性疾病(EBV+ PTLD)与挽救疗法相比的价值贡献为例:结果:Tabelecleucel 的贡献值为 0.63,反思讨论后增加到 0.75。EBV+PTLD被认为是一种威胁生命的疾病(5.0 ± 0.0),对已获批准的治疗方法的需求尚未得到满足(5.0 ± 0.0)。与挽救疗法相比,Tabelecleucel被认为在疗效(4.2 ± 0.8)和安全性(3.8 ± 0.8)方面都有所改善。大多数专家认为,与抢救疗法相比,高疗效和高安全性可提高患者的生活质量(2.3 ± 1.2),并节省医疗费用(2.3 ± 2.0)和非医疗费用(2.7 ± 1.6)。不过,也有人强调需要更多证据来证实这些改善和节省的时间。Tabelecleucel被认为有可能改变疾病的临床过程(4.3 ± 0.8),并得到高质量证据(3.2 ± 0.4)的支持。所有背景标准都对他贝鲁酮给予了高度肯定。"安全性/耐受性 "和 "其他医疗费用 "是反思性讨论后重新测试中变化最大的标准。反思性讨论解决了专家们的疑虑或误解,因此重新测试对 tabelecleucel 的价值贡献得出了更准确、更一致的结果:本研究表明,MCDA 方法是罕见病管理创新疗法决策的有用工具。研究还强调了多学科讨论反思的重要性,因为它能够解决专家的疑虑或误解,从而使药物的价值贡献获得更一致、更可靠的结果,并可能更加积极。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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