Philipp S, Menter A, Nikkels A F, Barber K, Landells I, Eichenfield L F, Song M, Randazzo B, Li S, Hsu M-C, Zhu Y, DePrimo S, Paller A S
Charite-Universitatsmedizin Berlin, Berlin, Germany.
Baylor Scott & White Health at Dallas, Dallas, TX, USA.
Br J Dermatol. 2020 Oct;183(4):664-672. doi: 10.1111/bjd.19018. Epub 2020 May 10.
Limited options are available for treatment of paediatric psoriasis.
To evaluate the efficacy and safety of ustekinumab in paediatric patients with psoriasis (≥ 6 to < 12 years of age).
CADMUS Jr, a phase III, open-label, single-arm, multicentre study, evaluated ustekinumab in paediatric patients with moderate-to-severe plaque psoriasis. Patients received weight-based dosing of ustekinumab (< 60 kg: 0·75 mg kg ; ≥ 60 to ≤ 100 kg: 45 mg; > 100 kg: 90 mg) administered by subcutaneous injection at weeks 0 and 4, then every 12 weeks through week 40. Study endpoints (all at week 12) included the proportions of patients achieving a Physician's Global Assessment score of cleared/minimal (PGA 0/1) and ≥ 75%/90% improvement in Psoriasis Area and Severity Index (PASI 75/90), and change in Children's Dermatology Life Quality Index (CDLQI). Serum ustekinumab concentrations, antidrug antibodies and cytokine levels were measured through week 52. Safety was evaluated through week 56.
In total, 44 patients (median age 9·5 years) received at least one dose of ustekinumab. Three patients discontinued the study agent through week 40. At week 12, 77% of patients achieved PGA 0/1, 84% achieved PASI 75 and 64% achieved PASI 90 response. The mean change in CDLQI was -6·3. Trough serum ustekinumab concentrations reached steady state at weeks 28-52. The incidence of antidrug antibodies was 10% (n = 4). Mean serum concentrations of interleukin-17A/F and interleukin-22 were significantly reduced at weeks 12 and 52. Overall, 34 patients (77%) had at least one adverse event and three (7%) had a serious adverse event.
Ustekinumab effectively treated moderate-to-severe psoriasis in paediatric patients, and no new safety concerns were identified. What is already known about this topic? Ustekinumab is approved for use in adolescents (≥ 12 to < 18 years of age) and adults (≥ 18 years) with moderate-to-severe psoriasis. What does this study add? Ustekinumab effectively treats moderate-to-severe psoriasis in paediatric patients (≥ 6 to < 12 years of age), with no new safety concerns. Linked Comment: Reich. Br J Dermatol 2020; 183:606-607.
儿童银屑病的治疗选择有限。
评估优特克单抗治疗6至12岁儿童银屑病患者的疗效和安全性。
CADMUS Jr是一项III期、开放标签、单臂、多中心研究,评估优特克单抗治疗中度至重度斑块状银屑病儿童患者的效果。患者接受基于体重的优特克单抗给药(<60kg:0.75mg/kg;≥60至≤100kg:45mg;>100kg:90mg),在第0周和第4周皮下注射给药,然后每12周给药一次,直至第40周。研究终点(均在第12周)包括达到医师整体评估清除/最小评分(PGA 0/1)以及银屑病面积和严重程度指数改善≥75%/90%(PASI 75/90)的患者比例,以及儿童皮肤病生活质量指数(CDLQI)的变化。在第52周前测量血清优特克单抗浓度、抗药抗体和细胞因子水平。在第56周前评估安全性。
共有44例患者(中位年龄9.5岁)接受了至少一剂优特克单抗。3例患者在第40周前停用了研究药物。在第12周时,77%的患者达到PGA 0/1,84%的患者达到PASI 75缓解,64%的患者达到PASI 90缓解。CDLQI的平均变化为-6.3。血清优特克单抗谷浓度在第28至52周达到稳态。抗药抗体的发生率为10%(n = 4)。在第12周和第52周时,白细胞介素-17A/F和白细胞介素-22的平均血清浓度显著降低。总体而言,34例患者(77%)至少发生一次不良事件,3例患者(7%)发生严重不良事件。
优特克单抗有效治疗儿童中度至重度银屑病,未发现新的安全问题。关于该主题已知的信息有哪些?优特克单抗已被批准用于治疗中度至重度银屑病的青少年(≥12至<18岁)和成人(≥18岁)。本研究补充了什么内容?优特克单抗有效治疗6至12岁儿童中度至重度银屑病,未发现新的安全问题。相关评论:Reich。《英国皮肤病学杂志》2020年;183:606 - 607。