A multicentre open-label study of apremilast in palmoplantar pustulosis (APLANTUS)

被引:15
作者
Wilsmann-Theis, D. [1 ]
Kromer, C. [2 ]
Gerdes, S. [3 ]
Linker, C. [4 ]
Magnolo, N. [5 ]
Sabat, R. [6 ]
Reich, K. [7 ]
Mossner, R. [2 ]
机构
[1] Univ Bonn, Dept Dermatol & Allergy, Bonn, Germany
[2] Univ Med Ctr Gottingen, Dept Dermatol, Gottingen, Germany
[3] Univ Med Ctr Schleswig Holstein Campus Kiel, Dept Dermatol, Ctr Inflammatory Skin Dis, Kiel, Germany
[4] TFS Clin, TFS Trial Form Support GmbH, Hamburg, Germany
[5] Univ Hosp Munster, Dept Dermatol, Munster, Germany
[6] Charite Univ Med Berlin, Psoriasis Res & Treatment Ctr, Berlin, Germany
[7] Univ Med Ctr Hamburg Eppendorf, Inst Hlth Serv Res Dermatol & Nursing, Translat Res Inflammatory Skin Dis, Hamburg, Germany
关键词
D O I
10.1111/jdv.17441
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background Palmoplantar pustulosis (PPP) is a chronic skin disease with painful erythematous scaly or crusty lesions and pustules on the palms and soles. Apremilast is a phosphodiesterase 4 inhibitor that has proven effective in the therapy of psoriasis, psoriatic arthritis and in oral ulcers associated with Behcet's disease. Objective To explore the efficacy of apremilast in PPP. Methods APLANTUS was a phase 2 single-arm multicentre study of apremilast in 21 subjects with moderate-to-severe PPP. Primary endpoint was the per cent change of the Palmoplantar Pustulosis Psoriasis Area and Severity Index (PPPASI) at week 20 compared to baseline. Results 20 weeks of oral treatment with apremilast in patients with moderate-to-severe PPP resulted in a significant decrease of the PPPASI with a median reduction of 57.1% (p < 0.001), and 61.9% of patients achieved at least a 50% improvement of the PPPASI relative to baseline. The total number of pustules per patient decreased significantly relative to baseline with 76.2% of patients achieving at least a 50% reduction in total pustules count at week 20. Improvement of PPP was also apparent in a significant decrease of the dermatologic life quality index (DLQI). The median DLQI score dropped from 8.5 at baseline to 2.0 at week 20 (p = 0.030). Apremilast was generally well tolerated, and no serious adverse events occurred. Conclusions Patients with PPP treated with apremilast showed benefit both in objective and subjective disease parameters. Apremilast should be investigated further in this difficult-to-treat skin condition. EudraCT number: 2016-005122-11.
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收藏
页码:2045 / 2050
页数:6
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