Suppr超能文献

芳香族 L-氨基酸脱羧酶(AADC)缺乏症的 Eladocagene Exuparvovec 与标准护理的长期结局比较:一项建模研究。

Long-Term Outcomes of Eladocagene Exuparvovec Compared with Standard of Care in Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency: A Modelling Study.

机构信息

OPEN Health; Evidence & Access, UK, 20 Old Bailey, London, EC4M 7AN, UK.

Department of Medical Genetics and Pediatrics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.

出版信息

Adv Ther. 2023 Dec;40(12):5399-5414. doi: 10.1007/s12325-023-02689-6. Epub 2023 Oct 6.

Abstract

INTRODUCTION

Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare disease with symptoms including movement disorders, developmental delays, and autonomic symptoms starting from birth; further, patients with AADC deficiency are at a high risk of death in the first decade of life. Limited information on the impact of treatment with gene therapy on patients' disease trajectories and survival, quality-of-life, and resource usage benefits are available.

METHOD

A cohort-based model with a lifetime horizon has been developed, based on motor milestones, to estimate the long-term benefits for patients after treatment with eladocagene exuparvovec compared to best supportive care (BSC). The model takes a National Health Service (NHS) perspective using a UK setting. The model comprises two parts: the developmental phase, in which patients with initially no motor function can progress to other motor milestone states, and a long-term projection phase. Efficacy for eladocagene exuparvovec is derived from clinical trial data with a duration up to 120 months. As the incidence of AADC deficiency is low, data for key model inputs is lacking; therefore estimates of survival by motor milestone were based on proxy diseases. A disease-specific utility study provided quality of life inputs and a burden of illness study informed inputs for disease management.

RESULTS

The model indicates survival (25.25 undiscounted life years gained) and quality-of-life benefits (20.21 undiscounted quality-adjusted life years [QALYs] gained) for patients treated with eladocagene exuparvovec compared to BSC. Resource usage costs are greater for patients treated with eladocagene exuparvovec, mainly due to the increased life expectancy during which patients accrue additional healthcare resource usage. Scenario analyses indicate robust results.

CONCLUSION

This study assessed long-term outcomes for patients with AADC deficiency. Patients treated with eladocagene exuparvovec were found to have improved survival and quality of life benefits compared to patients treated with BSC.

摘要

简介

芳香族 L-氨基酸脱羧酶(AADC)缺乏症是一种罕见疾病,其症状包括运动障碍、发育迟缓以及从出生开始就出现的自主症状;此外,AADC 缺乏症患者在生命的第一个十年中有很高的死亡风险。目前关于基因治疗对患者疾病轨迹和生存、生活质量以及资源使用效益的影响的信息有限。

方法

本研究基于运动里程碑,建立了一个基于队列的终生模型,以评估与最佳支持治疗(BSC)相比,接受埃拉多卡基因治疗的患者的长期获益。该模型从英国国民保健制度(NHS)的角度出发,采用英国的设定。该模型由两部分组成:发育阶段,在此阶段,最初没有运动功能的患者可以进展到其他运动里程碑状态,以及长期预测阶段。埃拉多卡基因治疗的疗效源自临床试验数据,其持续时间长达 120 个月。由于 AADC 缺乏症的发病率较低,因此关键模型输入数据缺乏;因此,基于代理疾病来估计患者的生存率。一项疾病特异性效用研究提供了生活质量的输入,一项疾病负担研究则为疾病管理的输入提供了信息。

结果

该模型表明,与 BSC 相比,接受埃拉多卡基因治疗的患者具有生存(25.25 个未经贴现的生命年获益)和生活质量(20.21 个未经贴现的质量调整生命年[QALY]获益)的获益。接受埃拉多卡基因治疗的患者的资源使用成本更高,主要是因为患者的预期寿命延长,在此期间他们会额外使用医疗保健资源。情景分析表明结果稳健。

结论

本研究评估了 AADC 缺乏症患者的长期结局。与 BSC 相比,接受埃拉多卡基因治疗的患者的生存率和生活质量均得到改善。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验