School of Medicine, University of Split, Šoltanska 2, 21000, Split, Croatia.
Cochrane Croatia, Šoltanska 2, 21000, Split, Croatia.
Syst Rev. 2024 Apr 19;13(1):110. doi: 10.1186/s13643-024-02522-3.
Vitiligo is a disease that affects people of all skin shades and can impact their quality of life. Reliable evidence on the effectiveness and adverse events associated with the recent use of Janus kinase (JAK) inhibitors to treat vitiligo is needed. This protocol for a systematic review and meta-analysis seeks to collect evidence from both randomized controlled trials (RCTs) and observational studies to determine the effectiveness and patient-centered outcomes concerning treatment with JAK inhibitors.
We will conduct a systematic review of the literature for RCTs and observational studies that used upadacitinib, ritlecitinib, brepocitinib, ifidancitinib, cerdulatinib, deglocitinib, baricitinib, tofacitinib, and ruxolitinib JAK inhibitors as treatments for vitiligo compared to placebo, no treatment, or combination therapies. We will systematically search from inception in Epistemonikos, MEDLINE, Scopus, Cochrane Central Register of Controlled Trials, EMBASE, ClinicalTrials.gov, PsycINFO, Allied and Complementary Medicine Database, Latin American and Caribbean Health Sciences Literature, Web of Science Core Collection, relevant preprint servers, and the gray literature. Ethics approval was not sought as the protocol and systematic review will not involve human participants, but rather summarized and anonymous data from studies. Primary outcomes include quality of life, percentage repigmentation, decreased vitiligo within 1 year or more, lasting repigmentation after a 2-year follow-up, cosmetic acceptability of repigmentation and tolerability or burden of treatment, and adverse events. Secondary outcomes are patient and study characteristics. We will include full-text articles, preprints, and clinical trial data in any language and all geographic regions. For data sources unavailable in English, we will obtain translations from global collaborators via the Cochrane Engage network. We will exclude articles for which sufficient information cannot be obtained from the authors of articles and systematic reviews. At least two investigators will independently assess articles for inclusion and extract data; reliability will be assessed before subsequent selection and data extraction of remaining studies. The risk of bias and certainty of evidence with Grading of Recommendations Assessment, Development, and Evaluation guidelines will be assessed independently by at least two investigators. We will estimate treatment effects by random-effects meta-analyses and assess heterogeneity using I. Data that cannot be included in the meta-analysis will be reported narratively using themes.
The proposed systematic review and meta-analysis describe the methods for summarizing and synthesizing the evidence on the effectiveness and patient-centered outcomes concerning the treatment of vitiligo with JAK inhibitors that were recently approved for this indication. To disseminate further the results of our systematic review, we plan to present them at international conferences and meetings. Our findings will provide robust evidence to facilitate decision-making at the policy or practitioner level.
PROSPERO CRD42023383920.
白癜风是一种影响所有肤色人群的疾病,会影响他们的生活质量。需要可靠的证据来评估最近使用 Janus 激酶(JAK)抑制剂治疗白癜风的疗效和不良反应。本系统评价和荟萃分析的方案旨在从随机对照试验(RCT)和观察性研究中收集证据,以确定 JAK 抑制剂治疗的疗效和以患者为中心的结局。
我们将对使用乌帕替尼、利特昔替尼、布罗昔替尼、依非替尼、塞德鲁替尼、德格洛替尼、巴瑞替尼、托法替布和鲁索替尼 JAK 抑制剂治疗白癜风的 RCTs 和观察性研究进行系统评价,这些研究将 JAK 抑制剂与安慰剂、无治疗或联合疗法进行比较。我们将系统地从 Epistemonikos、MEDLINE、Scopus、Cochrane 对照试验中心注册库、EMBASE、ClinicalTrials.gov、PsycINFO、补充和综合医学数据库、拉丁美洲和加勒比健康科学文献、Web of Science 核心合集、相关预印本服务器和灰色文献中进行检索。由于该方案和系统评价不会涉及人类参与者,而是总结和匿名来自研究的数据,因此不需要伦理批准。主要结局包括生活质量、色素再生百分比、1 年内或更长时间内白癜风减轻、2 年随访后持续色素再生、色素再生的美容可接受性和治疗的耐受性或负担,以及不良反应。次要结局是患者和研究特征。我们将包括来自任何语言和所有地理区域的全文文章、预印本和临床试验数据。对于无法用英语获得的数据源,我们将通过 Cochrane Engage 网络从全球合作者那里获取翻译。我们将排除那些无法从文章和系统评价的作者那里获得足够信息的文章。至少两名调查员将独立评估文章的纳入情况并提取数据;在对其余研究进行选择和数据提取之前,将评估可靠性。使用推荐评估、制定和评价指南(Grading of Recommendations Assessment, Development, and Evaluation)独立评估偏倚风险和证据确定性。我们将通过随机效应荟萃分析估计治疗效果,并使用 I 评估异质性。无法纳入荟萃分析的数据将使用主题进行叙述性报告。
本系统评价和荟萃分析描述了总结和综合最近批准用于治疗白癜风的 JAK 抑制剂的疗效和以患者为中心的结局证据的方法。为了进一步传播我们系统评价的结果,我们计划在国际会议和会议上展示。我们的研究结果将为政策制定者或从业者提供有力的证据,以帮助他们做出决策。
PROSPERO CRD42023383920。