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系统性硬化症临床试验中的患者报告结局指标

Patient-reported outcome instruments in clinical trials of systemic sclerosis.

作者信息

Pauling John D, Caetano Joana, Campochiaro Corrado, De Luca Giacomo, Gheorghiu Ana Maria, Lazzaroni Maria Grazia, Khanna Dinesh

机构信息

Royal National Hospital for Rheumatic Diseases, Bath, UK.

Department of Pharmacy & Pharmacology, University of Bath, Bath, UK.

出版信息

J Scleroderma Relat Disord. 2020 Jun;5(2):90-102. doi: 10.1177/2397198319886496. Epub 2019 Nov 25.

Abstract

Patient-reported outcome instruments provide valuable insight into disease-related morbidity known only to the patient and complement more objective outcome tools in the clinical trial setting. They are of particular importance in systemic sclerosis owing to the challenges around defining disease activity, the episodic nature of many disease-specific manifestations and the paucity of validated objective surrogate outcome measures for use in clinical trials. Early clinical trials of systemic sclerosis often incorporated legacy patient-reported outcome instruments, but the last 20 years has witnessed the emergence of several scleroderma-specific instruments that are now being routinely used alongside other outcomes in systemic sclerosis clinical trials. More recently, the value of patient-reported outcomes has been highlighted by their prominence in the American College of Rheumatology Combined Response Index for Systemic Sclerosis that has been utilized as the primary endpoint of recent clinical trials of early diffuse systemic sclerosis. This review considers the role and performance of the various patient-reported outcome instruments utilized in systemic sclerosis clinical trials, the current positioning of patient-reported outcome instruments within clinical trial endpoint models across the range of systemic sclerosis disease manifestations and, where applicable, we shall highlight areas for future research.

摘要

患者报告结局工具能为仅患者知晓的疾病相关发病率提供有价值的见解,并在临床试验环境中补充更为客观的结局工具。由于在定义疾病活动方面存在挑战、许多疾病特异性表现具有发作性特点以及用于临床试验的经过验证的客观替代结局指标匮乏,这些工具在系统性硬化症中尤为重要。系统性硬化症的早期临床试验通常纳入传统的患者报告结局工具,但在过去20年中,出现了几种硬皮病特异性工具,目前它们在系统性硬化症临床试验中与其他结局指标一起被常规使用。最近,患者报告结局的价值因其在美国风湿病学会系统性硬化症综合反应指数中的突出地位而得到凸显,该指数已被用作近期早期弥漫性系统性硬化症临床试验的主要终点。本综述探讨了系统性硬化症临床试验中使用的各种患者报告结局工具的作用和性能,患者报告结局工具在系统性硬化症疾病表现范围内的临床试验终点模型中的当前定位,并且在适用的情况下,我们将突出未来研究的领域。

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