Biological and JAK inhibitor therapy outcomes for severe psoriasis in trisomy 21

被引:0
|
作者
O'Connor, Cathal [1 ,2 ]
Byrne, Berbie [3 ]
Roche, Darren [1 ]
O'Connell, Garret [4 ]
O'Connell, Michael [4 ]
Murphy, Michelle [1 ,2 ]
Bourke, John [1 ]
Lynch, Maeve [3 ]
Bennett, Mary [1 ]
机构
[1] South Infirm Victoria Univ Hosp, Dept Dermatol, Cork, Ireland
[2] Univ Coll Cork, Dept Med, Cork, Ireland
[3] Univ Hosp Limerick, Dept Dermatol, Limerick, Ireland
[4] Univ Hosp Waterford, Dept Dermatol, Waterford, Ireland
关键词
arthritis; immunology; obesity; Psoriasis; trisomy; 21; RISK;
D O I
10.1111/1346-8138.16851
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Little is known about biological outcomes for severe psoriasis in trisomy 21 (T21). Our aim was to review outcomes of patients with T21 and severe psoriasis treated with biologic or Janus kinase inhibitors (JAKi). Information on demographics, co-morbidities, and therapeutic responses was retrospectively collated. Twenty-one patients were identified (mean age 24.7 years). Ninety percent (18/20) of TNF alpha inhibitor trials failed. Almost two-thirds (7/11) of patients achieved an adequate response with ustekinumab. All three patients treated with tofacitinib achieved an adequate response following at least three biologic failures. The mean number of biologic/JAKi therapies received was 2.1 with overall survival of 36%. Eighty-one percent (17/21) of patients required conversion from their index biologic treatment due to failure. In patients with T21 and severe psoriasis, failure of TNF alpha inhibition is common and ustekinumab therapy should be considered as first-line therapy. The role of JAKi is emerging.
引用
收藏
页码:1339 / 1342
页数:4
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