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A multicentre open-label study of apremilast in palmoplantar pustulosis (APLANTUS).
Wilsmann-Theis, D; Kromer, C; Gerdes, S; Linker, C; Magnolo, N; Sabat, R; Reich, K; Mössner, R.
Afiliación
  • Wilsmann-Theis D; Department of Dermatology and Allergy, University of Bonn, Bonn, Germany.
  • Kromer C; Department of Dermatology, University Medical Center Göttingen, Göttingen, Germany.
  • Gerdes S; Center for Inflammatory Skin Diseases, Department of Dermatology, University Medical Center Schleswig-Holstein Campus Kiel, Kiel, Germany.
  • Linker C; TFS Clinic, TFS Trial Form Support GmbH, Hamburg, Germany.
  • Magnolo N; Department of Dermatology, University Hospital Münster, Münster, Germany.
  • Sabat R; Psoriasis Research and Treatment Centre, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Reich K; Translational Research in Inflammatory Skin Diseases, Institute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Mössner R; Department of Dermatology, University Medical Center Göttingen, Göttingen, Germany.
J Eur Acad Dermatol Venereol ; 35(10): 2045-2050, 2021 Oct.
Article en En | MEDLINE | ID: mdl-34077577
ABSTRACT

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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Psoriasis / Enfermedades Cutáneas Vesiculoampollosas / Inhibidores de Fosfodiesterasa 4 Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Psoriasis / Enfermedades Cutáneas Vesiculoampollosas / Inhibidores de Fosfodiesterasa 4 Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Año: 2021 Tipo del documento: Article