Department of Dermatology, New Cross Hospital, The Royal Wolverhampton NHS Trust, Wolverhampton, UK.
Department of Dermatology, Henri Mondor University Hospital, Créteil, France.
Br J Dermatol. 2023 Feb 10;188(2):247-258. doi: 10.1093/bjd/ljac074.
In 2015, a major achievement in vitiligo research was the development of an internationally agreed upon core outcome domain set for randomized clinical trials (RCTs). Three outcomes were identified as being essential: repigmentation, side-effects/harms and maintenance of gained repigmentation. Four items were further recommended for inclusion. The following recommendations then followed: repigmentation should be assessed by measuring the percentage of repigmentation in quartiles (0-25%, 26-50%, 51-79%, 80-100%) and cosmetic acceptability of the results should be assessed using the Vitiligo Noticeability Scale.
The primary objective of this study was to assess uptake of the core outcome domain set for RCTs in vitiligo. Secondary objectives were to update the systematic review on outcomes reported in vitiligo RCTs, and to assess whether repigmentation and cosmetic acceptability of the results were measured using the above-mentioned recommended scales.
We searched PubMed, Cochrane Library (CENTRAL and Systematic Reviews) and ClinicalTrials.gov for vitiligo RCTs between November 2009 and March 2021. Screening and data extraction were independently performed on title and summary by two researchers. All outcomes and outcome measures reported in eligible RCTs were retrieved and collated.
In total, 174 RCTs were identified: 62 were published between 2009 and 2015, and 112 were published between 2016 and 2021.Thirty-eight different outcomes were reported. Repigmentation was the primary outcome in 89% of trials (150 of 169). Forty-nine different tools were used to measure repigmentation. Side-effects and harms were reported in 78% of trials (136 of 174). Maintenance of gained repigmentation was reported in only 11% of trials (20 of 174) and duration of follow-up varied greatly from 1 to 14 months. Cosmetic acceptability of the results and cessation of disease activity were assessed in only 2% of trials (four of 174). Quality of life of patients with vitiligo was assessed in 13% of trials (22 of 174). Finally, only 11 of 112 RCTs (10%) published between 2016 and 2021 reported all three essential core outcome domains (repigmentation, side-effects and maintenance of gained repigmentation) and none of the trials reported both essential and recommended core outcome domains.
Efforts are still needed to close the gap between set recommendations and RCT outcome reporting.
2015 年,在白癜风研究方面取得了一项重大成果,即制定了国际公认的随机临床试验(RCT)核心结局领域标准。确定了三个必不可少的结局:复色、副作用/伤害和维持获得的复色。还进一步推荐包括四个项目。随后提出了以下建议:复色应通过测量四分位法(0-25%、26-50%、51-79%、80-100%)的复色百分比进行评估,并且可以使用白癜风可见性量表评估结果的美容可接受性。
本研究的主要目的是评估 RCT 中白癜风核心结局领域标准的采用情况。次要目标是更新关于白癜风 RCT 报告结局的系统评价,并评估是否使用上述推荐的量表来衡量复色和结果的美容可接受性。
我们在 2009 年 11 月至 2021 年 3 月期间在 PubMed、Cochrane 图书馆(CENTRAL 和系统评价)和 ClinicalTrials.gov 中搜索了白癜风 RCTs。两名研究人员分别独立对标题和摘要进行筛选和数据提取。检索并整理了合格 RCTs 中报告的所有结局和结局测量指标。
共确定了 174 项 RCT:62 项发表于 2009 年至 2015 年期间,112 项发表于 2016 年至 2021 年期间。报告了 38 种不同的结局。复色是 89%(150/169)试验的主要结局。使用了 49 种不同的工具来衡量复色。78%(174/222)的试验报告了副作用和伤害。只有 11%(174/1578)的试验报告了维持获得的复色,随访时间从 1 至 14 个月不等。仅 2%(174/8694)的试验评估了结果的美容可接受性和疾病活动的停止。13%(174/13239)的试验评估了白癜风患者的生活质量。最后,2021 年期间发表的 112 项 RCT 中只有 11 项(10%)报告了所有三个必要的核心结局领域(复色、副作用和维持获得的复色),并且没有一项试验报告了必要和推荐的核心结局领域。
仍需要努力缩小既定建议和 RCT 结局报告之间的差距。