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Ustekinumab for the treatment of moderate-to-severe plaque psoriasis in paediatric patients (≥ 6 to < 12 years of age): efficacy, safety, pharmacokinetic and biomarker results from the open-label CADMUS Jr study.

Authors :
Philipp S
Menter A
Nikkels AF
Barber K
Landells I
Eichenfield LF
Song M
Randazzo B
Li S
Hsu MC
Zhu Y
DePrimo S
Paller AS
Source :
The British journal of dermatology [Br J Dermatol] 2020 Oct; Vol. 183 (4), pp. 664-672. Date of Electronic Publication: 2020 May 10.
Publication Year :
2020

Abstract

Background: Limited options are available for treatment of paediatric psoriasis.&lt;br /&gt;Objectives: To evaluate the efficacy and safety of ustekinumab in paediatric patients with psoriasis (≥ 6 to &lt; 12 years of age).&lt;br /&gt;Methods: 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 (&lt; 60 kg: 0&#183;75 mg kg &lt;superscript&gt;-1&lt;/superscript&gt; ; ≥ 60 to ≤ 100 kg: 45 mg; &gt; 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&#39;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&#39;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.&lt;br /&gt;Results: In total, 44 patients (median age 9&#183;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&#183;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.&lt;br /&gt;Conclusions: 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 &lt; 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 &lt; 12 years of age), with no new safety concerns. Linked Comment: Reich. Br J Dermatol 2020; 183:606-607.&lt;br /&gt; (&#169; 2020 The Authors. British Journal of Dermatology published by John Wiley &amp; Sons Ltd on behalf of British Association of Dermatologists.)

Details

Language :
English
ISSN :
1365-2133
Volume :
183
Issue :
4
Database :
MEDLINE
Journal :
The British journal of dermatology
Publication Type :
Academic Journal
Accession number :
32173852
Full Text :
https://doi.org/10.1111/bjd.19018