使用阿普雷米司特治疗牛皮癣:印度人对现实世界的看法。

IF 5.2 Q1 DERMATOLOGY Psoriasis (Auckland, N.Z.) Pub Date : 2021-08-14 eCollection Date: 2021-01-01 DOI:10.2147/PTT.S320810
Murlidhar Rajagopalan, Sunil Dogra, Abir Saraswat, Sachin Varma, Pravin Banodkar
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引用次数: 8

摘要

Apremilast是一种口服磷酸二酯酶-4抑制剂,被批准用于治疗银屑病和银屑病关节炎。尽管其有效性和安全性已在临床研究中得到很好的证实,但在现实环境中,不同的实践情况已被报道。这篇综述论文旨在评估临床现实世界的情况和治疗方面,这些信息在文献中被认为是缺乏或有争议的。根据文献综述,一个由五名专业治疗牛皮癣的皮肤科医生组成的小组考虑了五种情况;即阿普米司特在银屑病中的定位、在难治地区、特殊条件和人群中的应用、安全性、剂量滴定和维持治疗中的剂量。然后由印度的牛皮癣专家使用基于网络的问卷进行评估。关于这些情景,共讨论了28个问题。根据反应,阿普米司特对稳定的轻至中度牛皮癣单药治疗有效,对重度牛皮癣联合治疗有效。此外,对于它在头皮、手掌和脚底等困难部位的效果,也收到了积极的反应。为了减少不良反应,需要延长4周以上的滴定治疗,并可规定低剂量以维持缓解。阿普米司特一旦开始治疗,应至少持续8周,以达到预期效果,总治疗时间约为24周,以获得更好的疗效。它在许多其他情况下也有效,如肥胖患者,乙型或丙型肝炎和艾滋病毒患者,或服用多种药物的患者。据报道,阿普雷米司特比其他常规和生物系统治疗需要更少的预筛选和监测。总的来说,阿普雷米司特是个体化治疗牛皮癣的一个有吸引力的选择,因为它具有良好的安全性,口服给药方便,不需要筛查或持续的实验室监测,并且对难以治疗的区域的症状和病变有积极的影响。
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The Use of Apremilast in Psoriasis: An Indian Perspective on Real-World Scenarios.

Apremilast, an oral phosphodiesterase-4 inhibitor, is approved for use in the management of psoriasis and psoriatic arthritis. Although its efficacy and safety have been well established in clinical studies, in real-world settings, different practice scenarios have been reported. This review paper serves to evaluate clinical real-world scenarios and aspects of treatment for which the information in the literature was considered to be lacking or controversial. Following a literature review, a panel of five dermatologists with expertise in psoriasis considered five scenarios; namely, the positioning of apremilast in psoriasis, its use in difficult-to-treat areas, special conditions and populations, safety, dose titration and dose in maintenance therapy. These were then assessed with psoriasis experts in India using a web-based questionnaire. A total of 28 questions were discussed regarding these scenarios. According to the responses, apremilast is effective in stable mild to moderate psoriasis as monotherapy and in severe psoriasis in combination. Also, a positive response was received with regard to its effectiveness in difficult locations such as the scalp, palms and soles. To reduce adverse effects, prolonged titration therapy over 4 weeks is required and lower doses can be prescribed to maintain remission. Apremilast therapy should be continued for a minimum of 8 weeks once initiated to achieve the desired results, and the total duration of therapy should be about 24 weeks for better efficacy. It is also effective in many other cases, such as obese patients, patients with hepatitis B or C and HIV, or patients on polypharmacy. It was also reported that apremilast requires less prescreening and monitoring than other conventional and biologic systemic therapies. Overall, apremilast is an attractive option for the individualized treatment of psoriasis owing to its favorable safety profile, its ease of oral administration without the need for screening or ongoing laboratory monitoring, and its positive impact on symptoms and lesions in difficult-to-treat areas.

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