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首页> 外文期刊>The Journal of dermatological treatment >Efficacy, tolerability and safety of switching from etanercept to infliximab for the treatment of moderate-to-severe psoriasis: A multicenter, open-label trial (TANGO)
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Efficacy, tolerability and safety of switching from etanercept to infliximab for the treatment of moderate-to-severe psoriasis: A multicenter, open-label trial (TANGO)

机译:从依那西普转用英夫利昔单抗治疗中度至重度牛皮癣的疗效,耐受性和安全性:一项多中心,开放标签试验(TANGO)

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摘要

Biologic anti-tumor necrosis factor-alpha (anti-TNF-alpha) therapies have revolutionized the management of psoriasis. However, despite similar mechanisms of action, inter-patient variability in the clinical responses to therapy remain unexplained. Possible differences between agents include stability or bioavailability and anti-drug antibody development, and patient factors such as compliance may play a role. As a result, it is not uncommon for physicians to switch a patient from one anti-TNF-alpha agent to another when initial response is inadequate. This multicenter, single-arm, observational, Phase IV study assessed the efficacy and safety of infliximab therapy in patients with moderate-to-severe psoriasis who had not responded to 24 weeks' etanercept treatment. Drug efficacy was assessed using specific psoriasis indexes; health-related quality of life (HRQoL) was measured using the Dermatology Life Quality Index and the Skindex-29. A total of 48 patients were screened, 38 were treated with infliximab and 31 completed the study. Of these, 71% achieved Psoriasis Area and Severity Index 75 after 10 weeks, and improvement in HRQoL was documented. The results of this study showed that patients with moderate-to-severe psoriasis could be successfully switched from etanercept to infliximab, with improvements in both clinical parameter and HRQoL.
机译:生物抗肿瘤坏死因子-α(抗-TNF-α)治疗彻底改变了牛皮癣的治疗方法。然而,尽管有类似的作用机制,但患者对治疗的临床反应的可变性仍无法解释。药物之间的可能差异包括稳定性或生物利用度以及抗药物抗体的产生,而患者的依从性等因素可能起作用。结果,当初始反应不足时,医生会将患者从一种抗TNF-α药物转换为另一种抗肿瘤药物并不罕见。这项多中心,单臂,观察性IV期研究评估了英夫利昔单抗治疗对24周依那西普治疗无反应的中重度牛皮癣患者的疗效和安全性。使用特定的牛皮癣指数评估药物疗效;使用皮肤病生活质量指数和Skindex-29测量与健康有关的生活质量(HRQoL)。总共筛选了48位患者,其中38位接受了英夫利昔单抗治疗,其中31位完成了研究。其中有71%的患者在10周后达到了牛皮癣面积和严重性指数75,并且有HRQoL改善的记录。这项研究的结果表明,中度至重度银屑病患者可以成功地从依那西普转换为英夫利昔单抗,同时改善临床参数和HRQoL。

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