Department of Dermatology, University of Rome Tor Vergata, Italy.
Department of Dermatology, Radboud University Medical Centre, Nijmegen, the Netherlands.
Br J Dermatol. 2017 Aug;177(2):489-496. doi: 10.1111/bjd.15387. Epub 2017 Jun 22.
Little is known about the role of the HLA-C*06 allele in the response to psoriasis treatments.
To confirm the role of HLA-C*06 as a pharmacogenetic marker of response to ustekinumab in a new, large cohort of patients involving four European centres.
In this retrospective multicentre study we reviewed data of 255 patients with psoriasis genotyped for HLA-C*06 who started ustekinumab treatment between January 2014 and March 2015. The severity of psoriasis and response to treatment were evaluated using the Psoriasis Area and Severity Index (PASI) score at baseline and then at follow-up visits on weeks 4, 12, 28, 40 and 52. The primary end point was the proportion of patients achieving ≥ 50% reduction in PASI score (PASI 50) at week 4. A ≥ 75% reduction in PASI score (PASI 75) and a ≥ 90% reduction in the PASI score (PASI 90) after 12 weeks were secondary end points.
At week 4, PASI 50 was seen in 71·7% of HLA-C06-positive (C06POS) and 35·2% of HLA-C06-negative (C06NEG) patients. At week 12, PASI 75 was reached by 69.1% of C06POS patients and 40·5% of C06NEG patients. After 52 weeks, PASI 75 was reached by 83.7% of C06POS patients and 58.8% of C06NEG patients.
The results from our new, large cohort of European patients treated with ustekinumab in daily clinical practice confirm the role of HLA-C*06 as a potential predictor of response to ustekinumab.
关于 HLA-C*06 等位基因在银屑病治疗反应中的作用知之甚少。
在涉及四个欧洲中心的新的大型患者队列中,确认 HLA-C*06 作为乌司奴单抗治疗反应的药物遗传学标志物的作用。
在这项回顾性多中心研究中,我们回顾了 2014 年 1 月至 2015 年 3 月期间开始接受乌司奴单抗治疗的 255 例银屑病患者的 HLA-C*06 基因型数据。使用基线时和随访时(第 4、12、28、40 和 52 周)的银屑病面积和严重程度指数(PASI)评分评估银屑病的严重程度和治疗反应。主要终点是第 4 周时达到 PASI 评分降低≥50%(PASI 50)的患者比例。次要终点为第 12 周时 PASI 评分降低≥75%(PASI 75)和 PASI 评分降低≥90%(PASI 90)。
第 4 周时,HLA-C06 阳性(C06POS)患者的 PASI 50 为 71.7%,HLA-C06 阴性(C06NEG)患者为 35.2%。第 12 周时,C06POS 患者的 PASI 75 为 69.1%,C06NEG 患者为 40.5%。第 52 周时,C06POS 患者的 PASI 75 为 83.7%,C06NEG 患者为 58.8%。
来自我们新的、大型的欧洲患者队列的结果证实了 HLA-C*06 作为乌司奴单抗治疗反应的潜在预测因子的作用。