Ustekinumab in Real-Life Practice: Experience in 116 Patients with Moderate-To-Severe Psoriasis

被引:6
|
作者
Raposo, Ines [1 ]
Bettencourt, Andreia [2 ]
Leite, Luiz [3 ]
Selores, Manuela [1 ,4 ,5 ]
Torres, Tiago [1 ,4 ,5 ]
机构
[1] Ctr Hosp Porto, Dept Dermatol, Porto, Portugal
[2] Univ Porto, Inst Ciencias Biomed Abel Salazar, Immunogenet Lab, Porto, Portugal
[3] Clin Laser Belem, Lisbon, Portugal
[4] Univ Porto, Inst Ciencias Biomed Abel Salazar, Porto, Portugal
[5] Ctr Hosp Porto, Dermatol Res Unit, Porto, Portugal
来源
ACTA MEDICA PORTUGUESA | 2019年 / 32卷 / 03期
关键词
Biological Products/therapeutic use; Psoriasis/drug therapy; Ustekinumab/therapeutic use; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; LONG-TERM EFFICACY; DOUBLE-BLIND; SAFETY; TRIAL; ADJUSTMENT; CONSENSUS;
D O I
10.20344/amp.10728
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Ustekinumab is a monoclonal antibody directed against the p40 subunit common to both IL-12 and IL-23 cytokines. Although the evidence of ustekinumab efficacy and safety in clinical trials is extensively recognized, data on its use in clinical practice is limited. Our objective is to report on the real-life experience of two Portuguese dermatology departments with ustekinumab in patients with moderate to severe psoriasis, and to identify the clinical characteristics associated with a weaker clinical response. Material and Methods: Clinical, demographic, and therapeutic response data was retrospectively collected in 116 patients with moderate to severe psoriasis treated with ustekinumab between November 2009 and December 2015. Results: A PASI75 therapeutic response was observed in 67.2%, 85.3%, 89.6% and 88.7% of patients at weeks 4, 12, 24 and 52, respectively. Ustekinumab was discontinued in seven patients (three due to primary failure, three due to secondary treatment failure, and one due to adverse events). Neither cardiovascular events nor cases of reactivation of previous infections (tuberculosis, hepatitis B) were observed during follow-up. In nine patients methotrexate was used as adjuvant therapy, and fourteen patients required ustekinumab dosage optimization. No side effects were observed in the two latter groups. The therapeutic response was higher in patients naive to biologic therapies as compared to non-naive patients. Discussion and Conclusion: A trend towards lower clinical response was observed in patients weighing between 90-100 kg, and dosage optimization in this group of patients may be of value prior to considering biologic switch.
引用
收藏
页码:214 / 218
页数:5
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