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Efficacy and safety of ustekinumab in adolescents

机译:Ustekinumab在青少年中的疗效和安全性

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摘要

The biologic agent ustekinumab is a human monoclonal antibody that binds to the p40 subunit shared by interleukins (ILs) 12 and 23. The antibody is able to prevent binding of cytokines to the IL-12Rβ1 cell surface receptor and therefore may prevent IL-23 driven activation of the IL-23/Th 17 axis of inflammation. The anti-inflammatory activity has been beneficial in adult psoriasis. Ustekinumab has been approved in the United States for the treatment of adults with psoriasis and psoriatic arthritis. Approval in children and adolescents has not been granted by the US Food and Drug Administration. Subcutaneous injections of ustekinumab are administered at baseline, week 4 and every 12 weeks thereafter, a regimen that is particularly appealing to young patients who do not like more frequent injections at home. The product is attractive because, although it works through an immune system mechanism, the selective activity is such that the drug has not been associated with many of the side effects attributed to other immunosuppressive medications. Case reports of ustekinumab for pediatric psoriasis have shown promising results, and the recent Phase III CADMUS trial tested the agent in adolescents aged 12–17 years with psoriasis, using standard dose 0.75 mg/kg (≤60 kg), 45 mg (>60–≤100 kg), and 90 mg (>100 kg) or half-standard dosing 0.375 mg/kg (≤60 kg), 22.5 mg (>60–≤100 kg), and 45 mg (>100 kg) with a loading dosage at week 0 and week 4. Psoriasis area and severity index-75 was achieved in more than three-quarters of patients in full and half dosing by 12 weeks, and psoriasis area and severity index-90 in 54.1% and 61.1% of half and full dosage by 12 weeks, respectively. Ustekinumab was generally well tolerated in adolescents, with some patients developing antibodies, and nasopharyngitis being the major adverse event. Ustekinumab is a promising agent in adolescent psoriasis that appears to be well tolerated. The best monitoring plan and usage in younger patients still remain to be defined.
机译:生物制剂Ustekinumab是一种人单克隆抗体,可与白介素(ILs)12和23共有的p40亚基结合。该抗体能够防止细胞因子与IL-12Rβ1细胞表面受体结合,因此可以阻止IL-23驱动IL-23 / Th 17炎症轴的活化。抗炎活性在成人牛皮癣中是有益的。 Ustekinumab在美国已被批准用于治疗成人牛皮癣和牛皮癣关节炎。美国食品和药物管理局尚未批准对儿童和青少年进行批准。在基线,第4周和此后每12周给予ustekinumab皮下注射,该方案对于不喜欢在家中更频繁注射的年轻患者特别有吸引力。该产品之所以具有吸引力,是因为尽管它通过免疫系统机制起作用,但选择性活性使得该药物并未与其他免疫抑制药物引起的许多副作用相关。乌斯替单抗治疗小儿牛皮癣的病例报告显示了令人鼓舞的结果,最近的CADMUS III期试验在银屑病的12-17岁青少年中使用标准剂量0.75 mg / kg(≤60kg),45 mg(> 60 –≤100 kg)和90 mg(> 100 kg)或半标准剂量0.375 mg / kg(≤60kg),22.5 mg(>60-≤100kg)和45 mg(> 100 kg)在第0周和第4周的满负荷剂量下,到12周时,超过四分之三的患者在满负荷和半剂量的情况下达到了牛皮癣面积和严重程度指数为75,而牛皮癣面积和严重程度指数为90的患者分别达到了54.1%和61.1%分别在12周前减半和全剂量。 Ustekinumab通常在青少年中耐受良好,有些患者会产生抗体,而鼻咽炎是主要的不良事件。 Ustekinumab是青少年银屑病的有希望的药物,似乎耐受性良好。对于年轻患者的最佳监测计划和用法仍有待确定。

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