Omakase Consulting S.L., Barcelona y Madrid, Spain.
Hospital Universitario Virgen Macarena, Seville, Spain.
Orphanet J Rare Dis. 2024 Aug 23;19(1):308. doi: 10.1186/s13023-024-03324-5.
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.
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.
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.
本研究旨在通过多准则决策分析(MCDA)评估反思性多学科讨论对确定创新药物价值贡献的作用。该方法从相关利益相关者的角度出发,以全局、透明和系统的方式考虑所有与医疗保健决策相关的标准。使用 tabelecleucel 治疗 EBV 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确定作为示例。
tabelecleucel 的价值贡献评分为 0.63,经过反思性讨论后增加到 0.75。EBV PTLD 被认为是一种危及生命的疾病(5.0±0.0),对批准的治疗方法存在重大未满足的需求(5.0±0.0)。与挽救疗法相比,tabelecleucel 在疗效(4.2±0.8)和安全性(3.8±0.8)方面被认为具有改善。大多数专家认为,高疗效和安全性结果可能代表患者生活质量的改善(2.3±1.2),同时与挽救疗法相比,还可以节省医疗费用(2.3±2.0)和非医疗费用(2.7±1.6)。然而,其他人强调需要更多的证据来随着时间的推移确认这些改善和节省。tabelecleucel 被认为有可能改变疾病的临床过程(4.3±0.8),并得到高质量证据的支持(3.2±0.4)。所有背景标准都对 tabelecleucel 给予了高度积极的评价。“安全性/耐受性”和“其他医疗费用”是在反思性讨论后进行重新测试时变化最大的标准。反思性讨论有助于解决专家的疑虑或误解,因此重新测试获得了更准确和一致的 tabelecleucel 价值贡献结果。
本研究表明,MCDA 方法是用于决策管理罕见病创新治疗方法的有用工具。它还强调了反思性多学科讨论的重要性,因为它能够解决专家的疑虑或误解,从而获得更一致和可靠的药物价值贡献结果,潜在地更为积极。