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Apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the APROACH observational prospective study

To evaluate the effect of the phosphodiesterase 4 inhibitor apremilast in biologic-naïve patients with early peripheral PsA in terms of disease activity, clinical manifestations, patient-perceived outcomes, as well as apremilast’s safety profile in routine care settings of Greece. Non-interventional...

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Detalles Bibliográficos
Autores principales: Sfikakis, Petros P., Vassilopoulos, Dimitrios, Katsifis, Gkikas, Vosvotekas, Georgios, Dimitroulas, Theodoros, Sidiropoulos, Prodromos, Vounotrypidis, Periklis, Bogdanos, Dimitrios P., Georgountzos, Athanasios Ι., Bounas, Andreas G., Georgiou, Panagiotis, Gazi, Souzana, Kataxaki, Evangelia, Liossis, Stamatis-Nick, Theodorou, Evangelos, Papagoras, Charalampos, Theotikos, Evangelos, Vlachoyiannopoulos, Panayiotis, Voulgari, Paraskevi V., Kekki, Angeliki, Antonakopoulos, Nikolaos, Boumpas, Dimitrios T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073163/
https://www.ncbi.nlm.nih.gov/pubmed/36856816
http://dx.doi.org/10.1007/s00296-022-05269-z
Descripción
Sumario:To evaluate the effect of the phosphodiesterase 4 inhibitor apremilast in biologic-naïve patients with early peripheral PsA in terms of disease activity, clinical manifestations, patient-perceived outcomes, as well as apremilast’s safety profile in routine care settings of Greece. Non-interventional, multicenter, 52-week prospective cohort study, enrolling biologic-naïve patients with early active peripheral PsA who started apremilast after intolerance or inadequate response (within the first 12 months of treatment) to an initial conventional synthetic (cs)DMARD treatment. Non-responder imputation was applied for missing data.In total, 167 consecutive patients (mean age: 52.5 years; median PsA duration: 0.9 years) were analyzed. At baseline, the median (interquartile range) clinical Disease Activity in Psoriatic Arthritis (cDAPSA) score was 22.0 (16.0–29.0), with 86.8% of patients having at least moderate (29.3% high) disease activity; 87.4% had skin psoriasis, 37.7% nail psoriasis, 30.7% enthesitis, and 12.4% dactylitis. At 16, 24, and 52 weeks, 28.7, 42.5, and 48.5% of patients, achieved ≥ 50% improvement in their baseline cDAPSA score, respectively. At week 52, 55.6, 50, and 26.8% of evaluable patients achieved complete resolution of enthesitis, dactylitis and nail psoriasis, respectively. Improvements were also observed in patient’s health state assessed by the Psoriatic Arthritis Impact of Disease 12-item questionnaire, and health-related quality of life. The 52-week drug survival rate was 75%, while 13.8% of patients experienced at least one adverse drug reaction.Biologic-naïve patients with early PsA, treated with apremilast experienced significant improvements in disease activity, extra-articular manifestations and patient-centered outcomes, accompanied by a favorable tolerability profile. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00296-022-05269-z.