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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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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 |
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author | 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. |
author_facet | 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. |
author_sort | Sfikakis, Petros P. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10073163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100731632023-04-06 Apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the APROACH observational prospective study 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. Rheumatol Int Observational Research 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. Springer Berlin Heidelberg 2023-03-01 2023 /pmc/articles/PMC10073163/ /pubmed/36856816 http://dx.doi.org/10.1007/s00296-022-05269-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Observational Research 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. Apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the APROACH observational prospective study |
title | Apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the APROACH observational prospective study |
title_full | Apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the APROACH observational prospective study |
title_fullStr | Apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the APROACH observational prospective study |
title_full_unstemmed | Apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the APROACH observational prospective study |
title_short | Apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the APROACH observational prospective study |
title_sort | apremilast for biologic-naïve, peripheral psoriatic arthritis, including patients with early disease: results from the aproach observational prospective study |
topic | Observational Research |
url | 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 |
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