Fotiadou C, Lazaridou E, Sotiriou E, Kyrgidis A, Apalla Z, Ioannides D
First Department of Dermatology-Venereology, Aristotle University Medical School, Thessaloniki, Greece.
Department of Oral Maxillofacial Surgery, Aristotle University Medical School, Thessaloniki, Greece.
J Eur Acad Dermatol Venereol. 2016 Dec;30(12):2091-2096. doi: 10.1111/jdv.13780. Epub 2016 Jul 13.
The scalp is a frequent and difficult-to-treat localization of psoriasis. Little evidence exists regarding the use of biologic agents in recalcitrant cases of scalp psoriasis that are resistant to other treatment options.
To evaluate and compare the efficacy of currently available biologic agents (infliximab, etanercept, adalimumab, ustekinumab) in the treatment of scalp symptoms in patients suffering from moderate to severe plaque psoriasis.
This retrospective cohort study consisted of a review of the database of all psoriasis patients who suffered from scalp symptoms and received biologic treatment between January 2012 and December 2014. The patients were divided into four groups based on the drug administered. Scalp psoriasis severity was assessed by the Psoriasis Scalp Severity Index (PSSI) at baseline and at weeks 4, 12, 24 and 48. Psoriasis severity was evaluated with the Psoriasis Area and Severity Index (PASI) at the same time points.
In total, 145 patients were enroled in the study (infliximab n = 35, etanercept n = 30, adalimumab n = 39, ustekinumab n = 41). At week 4, the infliximab group achieved a 74% mean decrease in the PSSI (ΔPSSI), followed by mean decreases of 61.7%, 53.1% and 53.7% in the ustekinumab, etanercept and adalimumab groups respectively. The differences in the ΔPSSI were lower at week 48: ustekinumab 94.9%, infliximab 94.3%, etanercept 83.1% and adalimumab 89.0%. The PASI score improved sufficiently in all treatment groups. Infliximab and ustekinumab exhibited greater efficacy at weeks 4 and 12. This difference was not as prominent as that revealed by the PSSI. At week 48, the differences in the ΔPASI were barely statistically significant (P = 0.048).
All four biologic agents yielded significant improvement in both scalp and skin lesions. Ustekinumab and infliximab exhibited the greatest efficacy, which was clinically meaningful from the early stages of the study. Adalimumab and etanercept followed, yielding satisfactory improvement rates.
头皮是银屑病常见且难治的发病部位。对于对其他治疗方案耐药的顽固性头皮银屑病病例,使用生物制剂的证据较少。
评估和比较目前可用的生物制剂(英夫利昔单抗、依那西普、阿达木单抗、乌司奴单抗)对中度至重度斑块状银屑病患者头皮症状的治疗效果。
这项回顾性队列研究包括对2012年1月至2014年12月期间所有有头皮症状并接受生物治疗的银屑病患者数据库的回顾。根据所使用的药物将患者分为四组。在基线以及第4、12、24和48周时,通过银屑病头皮严重程度指数(PSSI)评估头皮银屑病的严重程度。在相同时间点用银屑病面积和严重程度指数(PASI)评估银屑病严重程度。
共有145例患者纳入研究(英夫利昔单抗组n = 35,依那西普组n = 30,阿达木单抗组n = 39,乌司奴单抗组n = 41)。在第4周时,英夫利昔单抗组的PSSI平均下降了74%(ΔPSSI),随后乌司奴单抗组、依那西普组和阿达木单抗组的平均下降率分别为61.7%、53.1%和53.7%。在第48周时,ΔPSSI的差异较小:乌司奴单抗组为94.9%,英夫利昔单抗组为94.3%,依那西普组为83.1%,阿达木单抗组为89.0%。所有治疗组的PASI评分均有充分改善。英夫利昔单抗和乌司奴单抗在第4周和第12周时疗效更佳。这种差异不如PSSI显示的那么显著。在第48周时,ΔPASI的差异几乎无统计学意义(P = 0.048)。
所有四种生物制剂均使头皮和皮肤病变有显著改善。乌司奴单抗和英夫利昔单抗疗效最佳,从研究早期就具有临床意义。其次是阿达木单抗和依那西普,改善率令人满意。