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Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort
Drug survival reflects treatment effectiveness and safety in real life. There is limited data on the variation of drug survival with the availability of systemic treatments with additional biological disease-modifying antirheumatic drugs (bDMARDs) or synthetic disease-modifying antirheumatic drugs (...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Society for Publication of Acta Dermato-Venereologica
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631244/ https://www.ncbi.nlm.nih.gov/pubmed/34806759 http://dx.doi.org/10.2340/actadv.v101.566 |
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author | BETTUZZI, Thomas BACHELEZ, Hervé BEYLOT-BARRY, Marie ARLÉGUI, Hugo PAUL, Carle VIGUIER, Manuelle MAHÉ, Emmanuel BENETON, Nathalie JULLIEN, Denis RICHARD, Marie-Aleth JOLY, Pascal TUBACH, Florence DUPUY, Alain SBIDIAN, Emilie CHOSIDOW, Olivier |
author_facet | BETTUZZI, Thomas BACHELEZ, Hervé BEYLOT-BARRY, Marie ARLÉGUI, Hugo PAUL, Carle VIGUIER, Manuelle MAHÉ, Emmanuel BENETON, Nathalie JULLIEN, Denis RICHARD, Marie-Aleth JOLY, Pascal TUBACH, Florence DUPUY, Alain SBIDIAN, Emilie CHOSIDOW, Olivier |
author_sort | BETTUZZI, Thomas |
collection | PubMed |
description | Drug survival reflects treatment effectiveness and safety in real life. There is limited data on the variation of drug survival with the availability of systemic treatments with additional biological disease-modifying antirheumatic drugs (bDMARDs) or synthetic disease-modifying antirheumatic drugs (sDMARDs). The aim of this study was to determine whether the increasing number of available systemic treatments for psoriasis affects drug survival over time. Patients were selected from the PsoBioTeq cohort, a French prospective observational cohort enrolling patients with moderate to severe psoriasis. All patients initiating a first bDMARD or sDMARD were included. The primary outcome was comparison of drug survival over time. A multivariate Cox proportional hazard ratio model was computed. A total of 1,866 patients were included; 739 females (39%), median age 47 years. In the multivariate Cox model, no association was found between the calendar year of initiation and drug survival (hazard ratio) overlapping from 0.80 (0.42–1.52) to 1.17 (0.64–2.17), p = 0.633). In conclusion, drug survival in psoriasis is not affected by the year of initiation. |
format | Online Article Text |
id | pubmed-9631244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Society for Publication of Acta Dermato-Venereologica |
record_format | MEDLINE/PubMed |
spelling | pubmed-96312442022-11-17 Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort BETTUZZI, Thomas BACHELEZ, Hervé BEYLOT-BARRY, Marie ARLÉGUI, Hugo PAUL, Carle VIGUIER, Manuelle MAHÉ, Emmanuel BENETON, Nathalie JULLIEN, Denis RICHARD, Marie-Aleth JOLY, Pascal TUBACH, Florence DUPUY, Alain SBIDIAN, Emilie CHOSIDOW, Olivier Acta Derm Venereol Original Article Drug survival reflects treatment effectiveness and safety in real life. There is limited data on the variation of drug survival with the availability of systemic treatments with additional biological disease-modifying antirheumatic drugs (bDMARDs) or synthetic disease-modifying antirheumatic drugs (sDMARDs). The aim of this study was to determine whether the increasing number of available systemic treatments for psoriasis affects drug survival over time. Patients were selected from the PsoBioTeq cohort, a French prospective observational cohort enrolling patients with moderate to severe psoriasis. All patients initiating a first bDMARD or sDMARD were included. The primary outcome was comparison of drug survival over time. A multivariate Cox proportional hazard ratio model was computed. A total of 1,866 patients were included; 739 females (39%), median age 47 years. In the multivariate Cox model, no association was found between the calendar year of initiation and drug survival (hazard ratio) overlapping from 0.80 (0.42–1.52) to 1.17 (0.64–2.17), p = 0.633). In conclusion, drug survival in psoriasis is not affected by the year of initiation. Society for Publication of Acta Dermato-Venereologica 2022-03-08 /pmc/articles/PMC9631244/ /pubmed/34806759 http://dx.doi.org/10.2340/actadv.v101.566 Text en © 2022 Acta Dermato-Venereologica https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the CC BY-NC license |
spellingShingle | Original Article BETTUZZI, Thomas BACHELEZ, Hervé BEYLOT-BARRY, Marie ARLÉGUI, Hugo PAUL, Carle VIGUIER, Manuelle MAHÉ, Emmanuel BENETON, Nathalie JULLIEN, Denis RICHARD, Marie-Aleth JOLY, Pascal TUBACH, Florence DUPUY, Alain SBIDIAN, Emilie CHOSIDOW, Olivier Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort |
title | Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort |
title_full | Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort |
title_fullStr | Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort |
title_full_unstemmed | Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort |
title_short | Evolution of Drug Survival with Biological Agents and Apremilast Between 2012 and 2018 in Patients with Psoriasis from the PsoBioTeq Cohort |
title_sort | evolution of drug survival with biological agents and apremilast between 2012 and 2018 in patients with psoriasis from the psobioteq cohort |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631244/ https://www.ncbi.nlm.nih.gov/pubmed/34806759 http://dx.doi.org/10.2340/actadv.v101.566 |
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