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分析临床试验负担和患者对改善大疱性表皮松解症临床研究的态度。

Profiling trial burden and patients' attitudes to improve clinical research in epidermolysis bullosa.

机构信息

Department of Dermatology and Allergology, University Hospital of the Paracelsus Medical University Salzburg, Muellner Hauptstrasse 48, 5020, Salzburg, Austria.

EB House Austria, Department of Dermatology and Allergology, University Hospital of the Paracelsus Medical University Salzburg, 5020, Salzburg, Austria.

出版信息

Orphanet J Rare Dis. 2020 Jul 10;15(1):182. doi: 10.1186/s13023-020-01443-3.

Abstract

BACKGROUND

Epidermolysis bullosa (EB) comprises inherited mechanobullous dermatoses with considerable morbidity and mortality. While current treatments are symptomatic, a growing number of innovative therapeutic compounds are evaluated in clinical trials. Clinical research in rare diseases like EB, however, faces many challenges, including sample size requirements and recruitment failures. The objective of this study was to determine attitudes of EB patients towards clinical research and trial participation as well as the assessment of contextual motivating and discouraging factors in an effort to support patient-centered RD trial designing.

METHODS

A 53-items questionnaire was handed over to EB patients (of all types and ages) in contact with the EB House Austria, a designated national center of expertise for EB care. Main categories included level of interest in and personal knowledge about clinical studies, pros/cons for participation and extent of individual expenses considered acceptable for participation in a clinical study. Descriptive subgroup analysis was calculated with SPSS 20.0 and Microsoft Excel.

RESULTS

Thirty-six individuals (mean age 25.7 years), diagnosed for recessive dystrophic EB (36.1%), EB simplex (33.4%), junctional EB (8.3%), dominant dystrophic EB (2.8%) and acral peeling syndrome (2.8%) participated. Motivation for participation in and the desire to increase personal knowledge about clinical trials were (outmost) high in 57.2 and 66.7%, respectively. Altruism was the major motivating factor, followed by hope that alleviation of the own symptoms can be achieved. The greatest hurdle was travel distance, followed by concerns about possible adverse reactions. Patients diagnosed for severe subgroups (RDEB, JEB) were more impaired by the extent of scheduled invasive investigations and possible adverse reactions of the study medication. Patients with generally milder EB forms and older patients were accepting more frequent outpatient study visits, blood takes, skin biopsies and inpatient admissions in association with trial participation.

CONCLUSIONS

This study provides additional indications to better determine and address attitudes towards clinical research among EB patients as well as guidance to improve clinical trial protocols for patient centricity.

摘要

背景

大疱性表皮松解症(EB)是一种遗传性机械性水疱性皮肤病,发病率和死亡率都很高。虽然目前的治疗方法是对症治疗,但越来越多的创新治疗药物正在临床试验中进行评估。然而,像 EB 这样的罕见病的临床研究面临着许多挑战,包括样本量要求和招募失败。本研究的目的是确定 EB 患者对临床研究和试验参与的态度,以及评估影响患者参与意愿的相关激励和阻碍因素,以支持以患者为中心的罕见病临床试验设计。

方法

向接触 EB 奥地利之家(一家指定的 EB 护理国家专业中心)的 EB 患者(各种类型和年龄)分发了一份包含 53 个项目的问卷。主要类别包括对临床研究的兴趣水平和个人了解程度、参与的利弊以及个人认为可接受的参与临床试验的费用。使用 SPSS 20.0 和 Microsoft Excel 进行描述性亚组分析。

结果

36 名个体(平均年龄 25.7 岁)参与了研究,他们被诊断为隐性营养不良性大疱性表皮松解症(36.1%)、单纯性大疱性表皮松解症(33.4%)、交界性大疱性表皮松解症(8.3%)、显性营养不良性大疱性表皮松解症(2.8%)和肢端性表皮松解症(2.8%)。参与临床研究的动力和增加对临床试验的个人了解的愿望非常高(分别为 57.2%和 66.7%)。利他主义是主要的激励因素,其次是缓解自身症状的希望。最大的障碍是旅行距离,其次是对可能的不良反应的担忧。被诊断为严重亚组(RDEB、JEB)的患者受到计划进行的侵入性检查和研究药物可能产生的不良反应的影响更大。一般来说病情较轻的 EB 患者和年龄较大的患者更容易接受更频繁的门诊研究访问、抽血、皮肤活检和住院治疗。

结论

本研究为更好地确定 EB 患者对临床研究的态度以及指导改善以患者为中心的临床试验方案提供了额外的依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43a8/7350741/2a28a05b07b9/13023_2020_1443_Fig1_HTML.jpg

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