Department of Dermatology, Radboud University Medical Centre, Radboud Institute of Health Sciences, Nijmegen, the Netherlands.
Department of Operating Rooms, Radboud University Medical Centre, Radboud Institute of Health Sciences, Nijmegen, the Netherlands.
JAMA Dermatol. 2019 Jun 1;155(6):708-715. doi: 10.1001/jamadermatol.2019.0098.
Previous research showed a differential response to ustekinumab therapy based on HLA-C*06:02 status in patients with psoriasis but consisted mostly of small (and sometimes inconclusive) cohort studies.
To assess whether HLA-C*06:02 status is associated with a differential response to ustekinumab therapy in patients with psoriasis through a systematic review and a meta-analysis of available data.
A comprehensive search was conducted using MEDLINE, Embase, the Cochrane Library, Web of Science, and gray literature sources. Databases were searched from January 1, 2000, to May 14, 2018. Search strategies included terms and synonyms for psoriasis, HLA-C, and ustekinumab. Languages were restricted to English, French, German, and Dutch.
Studies were included if they reported the association between HLA-C*06:02 status and 75% improvement in Psoriasis Area and Severity Index (PASI75) response to ustekinumab therapy in patients with plaque psoriasis after 6 and/or 3 months of treatment. Randomized clinical trials and observational studies were included. Screening and selection were performed independently by 2 reviewers.
HLA-C*06:02 genotype status and PASI75 response rates were extracted by 2 reviewers. Data were pooled using random-effects models. Heterogeneity was assessed using the τ2 and I2 statistic. Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) and Meta-Analysis of Observational Studies in Epidemiology (MOOSE) reporting guidelines were followed.
The primary outcome was the risk difference of achieving PASI75 after 6 months of ustekinumab therapy between HLA-C06:02-positive and HLA-C06:02-negative patients.
A total of 8 studies were reviewed; 1048 patients were included for meta-analyses, and 937 patients were included for the primary analysis of PASI75 response after 6 months of treatment. Random-effects meta-analysis showed a risk difference of 0.24 (95% CI, 0.14-0.35; P < .001) in favor of HLA-C06:02-positive patients. The median PASI75 response rate in the HLA-C06:02-positive group was 92% (pooled, 89%; range, 62%-98%). For HLA-C*06:02-negative patients, the median response rate was 67% (pooled, 62%; range, 40%-84%). Substantial heterogeneity may have been present, with an I2 of 82%.
The meta-analysis showed a differential response to ustekinumab therapy based on HLA-C06:02 status in patients with psoriasis. Although HLA-C06:02-positive patients had high PASI75 response rates after 6 months, the PASI75 response rate was also high in the HLA-C06:02-negative group. There appears to be no rationale for excluding patients from ustekinumab treatment based on a negative HLA-C06:02 status.
先前的研究表明,基于银屑病患者 HLA-C*06:02 状态,乌司奴单抗治疗有不同的反应,但这些研究大多是小样本(有时结论不确定)的队列研究。
通过系统评价和对现有数据的荟萃分析,评估 HLA-C*06:02 状态是否与银屑病患者乌司奴单抗治疗的不同反应相关。
使用 MEDLINE、Embase、Cochrane 图书馆、Web of Science 和灰色文献来源进行全面检索。从 2000 年 1 月 1 日至 2018 年 5 月 14 日,数据库进行了检索。搜索策略包括银屑病、HLA-C 和乌司奴单抗的术语和同义词。语言仅限于英语、法语、德语和荷兰语。
如果研究报告了 HLA-C06:02 状态与斑块状银屑病患者在接受乌司奴单抗治疗 6 个月和/或 3 个月后 75%的银屑病面积和严重性指数(PASI75)反应之间的关联,且纳入了 75%改善 PASI75 反应的 HLA-C06:02 阳性患者比例,则研究被纳入。纳入了随机临床试验和观察性研究。筛选和选择由 2 位评审员独立进行。
由 2 位评审员提取 HLA-C*06:02 基因型状态和 PASI75 反应率。使用随机效应模型对数据进行汇总。使用 τ2 和 I2 统计量评估异质性。遵循了系统评价和荟萃分析的首选报告项目(PRISMA)和观察性研究荟萃分析的 MOOSE 报告指南。
主要结局是 HLA-C06:02 阳性和 HLA-C06:02 阴性患者在接受乌司奴单抗治疗 6 个月后达到 PASI75 的风险差异。
共审查了 8 项研究;1048 名患者纳入荟萃分析,937 名患者纳入治疗 6 个月后 PASI75 反应的主要分析。随机效应荟萃分析显示,HLA-C06:02 阳性患者有 0.24(95%CI,0.14-0.35;P<0.001)的风险差异有利于 HLA-C06:02 阳性患者。HLA-C06:02 阳性组的中位 PASI75 反应率为 92%(汇总,89%;范围,62%-98%)。对于 HLA-C06:02 阴性患者,中位反应率为 67%(汇总,62%;范围,40%-84%)。可能存在大量异质性,I2 为 82%。
荟萃分析表明,银屑病患者基于 HLA-C06:02 状态对乌司奴单抗治疗有不同的反应。尽管 HLA-C06:02 阳性患者在接受乌司奴单抗治疗 6 个月后 PASI75 反应率较高,但 HLA-C06:02 阴性组的 PASI75 反应率也较高。似乎没有理由根据 HLA-C06:02 状态的阴性而排除患者接受乌司奴单抗治疗。