Efficacy and safety assessment of netakimab in scalp psoriasis

Q4 Medicine
M. I. Kurdina, N. G. Kolenko
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Abstract

Introduction . Scalp psoriasis is a common disease that has a long, recurrent course with severe desquamation, dryness and itching of the skin. The location of the pathological process in an aesthetically significant area, constant therapy leads to low satisfaction and adherence to treatment and, as a result, to a pronounced decrease in the quality of life. Aim . To study the efficacy and safety of netakimab in psoriasis of the scalp. Materials and methods . 52 adult patients (n = 52) with psoriasis of the face and scalp were under observation. The severity of the psoriatic lesion of the scalp was determined using the PSSI index (Psoriasis Severity Scalp Index). The assessment was carried out before the start of treatment, in the first week, and then every 4 weeks up to and including 52 weeks. The Dermatological Quality of Life Index (DLQI) – were determined by questionnaires before the start of treatment, at the 12th and 52nd weeks. All patients on an outpatient basis received netakimab monotherapy at a dose of 120 mg in the form of two subcutaneous injections of 1 ml (60 mg) of the drug, each administered once a week at weeks 0, 1 and 2, then 1 time every 4 weeks. The total duration of treatment for each patient was 1 year (52 weeks). The safety of netakimab was evaluated based on the development of adverse events and local reactions to the administration of the drug. Results . The results of the study (n = 52) for 52 weeks showed high efficacy of netakimab. 48% of patients achieved PSSI 90 by the week 12 of treatment and 77% of patients achieved PSSI 90 by the week 52, itching of the scalp significantly decreased and the quality of life improved. During the 52 weeks of the study, there were no cases of early withdrawal due to adverse events and cases of serious adverse events. Conclusion . Based on the study results we recommend netakimab for medical use among patients with moderate and severe scalp psoriasis.
奈他单抗治疗头皮牛皮癣的疗效及安全性评价
介绍。头皮牛皮癣是一种常见病,病程长,反复发作,伴有严重的皮肤脱屑、干燥和瘙痒。病理过程的位置在美学上重要的区域,持续的治疗导致低满意度和治疗依从性,结果,生活质量明显下降。的目标。目的:探讨奈他单抗治疗头皮银屑病的疗效和安全性。材料和方法。对52例面部及头皮银屑病患者进行观察。使用PSSI指数(头皮银屑病严重程度指数)确定头皮银屑病病变的严重程度。评估在治疗开始前、第一周进行,然后每4周进行一次,直至52周。在治疗开始前、第12周和第52周通过问卷调查确定皮肤生活质量指数(DLQI)。所有门诊患者均接受奈他单抗单药治疗,剂量为120mg,皮下注射1ml (60mg),分别在第0、1和2周每周给药一次,然后每4周给药一次。每例患者的总治疗时间为1年(52周)。该药物的安全性是根据不良事件的发生和局部给药反应来评估的。结果。52周的研究结果(n = 52)显示了奈他单抗的高疗效。48%的患者在治疗第12周达到PSSI 90, 77%的患者在治疗第52周达到PSSI 90,头皮瘙痒明显减少,生活质量得到改善。在52周的研究中,没有一例由于不良事件而早期停药的病例和严重不良事件的病例。结论。基于研究结果,我们推荐奈他单抗用于中度和重度头皮牛皮癣患者的医疗用途。
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来源期刊
Meditsinskiy Sovet
Meditsinskiy Sovet Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
418
审稿时长
6 weeks
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