A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients.
BACKGROUND: Secukinumab is a first-in-class interleukin 17A monoclonal antibody that has demonstrated an excellent safety and efficacy profile in phase 3 studies. OBJECTIVE: To evaluate the effectiveness of secukinumab in daily clinical practice and to understand the clinical and epidemiologic chara...
| Autores: | , , , , , , , , , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO) |
| Repositorio: | r-FISABIO. Repositorio Institucional de Producción Científica |
| OAI Identifier: | oai:fisabio.fundanetsuite.com:p3341 |
| Acceso en línea: | https://fisabio.portalinvestigacion.com/publicaciones/3341 |
| Access Level: | acceso abierto |
| Palabra clave: | IL-17 biologic therapy psoriasis secukinumab |
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A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients.Ortiz Salvador JMSaneleuterio Temporal MMagdaleno Tapial JManel VPConrad PMSahuquillo Torralba AMateu-Puchades, AlmudenaPitarch-Bort, GerardMari-Ruiz, Juan-IgnacioMataix Díaz JMontesinos Villaescusa EMiralles-Botella, JuliaGarcia-Fernandez, LauraMartorell Calatayud ABelinchon, I.Sánchez Carazo JLPérez Ferriols AIL-17biologic therapypsoriasissecukinumabBACKGROUND: Secukinumab is a first-in-class interleukin 17A monoclonal antibody that has demonstrated an excellent safety and efficacy profile in phase 3 studies. OBJECTIVE: To evaluate the effectiveness of secukinumab in daily clinical practice and to understand the clinical and epidemiologic characteristics of patients treated with secukinumab in clinical settings. METHODS: In this multicenter prospective observational study, we recruited adult patients with moderate-to-severe plaque psoriasis from 12 hospitals in Spain during January-December 2016. These patients were treated with secukinumab and prospectively followed at 12-week intervals for 52 weeks. RESULTS: In total, 158 patients were recruited to the study. A Psoriasis Area and Severity Index (PASI) score improvement =75% over baseline (PASI-75) was achieved by 57%, 83.5%, 89%, and 78.5% of patients at weeks 4, 12, 24, and 52, respectively. PASI-90 was achieved in 27.8%, 62%, 64.6%, and 63.2% of patients at weeks 4, 12, 24, and 52, respectively; PASI-75 and PASI-90 responders were significantly more common among patients with a body mass index <30 kg/cm(2) and patients without previous biologic therapy failures. LIMITATIONS: Observational study. Time from onset of psoriasis was not evaluated. CONCLUSION: Secukinumab is a safe treatment with effectiveness rates similar to those found in its phase 3 studies. These rates endure up to a year from start of treatment.MOSBY-ELSEVIER2019info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://fisabio.portalinvestigacion.com/publicaciones/3341JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGYISSN: 01909622ISSNe: 10976787reponame:r-FISABIO. Repositorio Institucional de Producción Científicainstname:Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)Inglésinfo:eu-repo/semantics/openAccessoai:fisabio.fundanetsuite.com:p33412026-06-11T12:45:17Z |
| dc.title.none.fl_str_mv |
A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients. |
| title |
A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients. |
| spellingShingle |
A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients. Ortiz Salvador JM IL-17 biologic therapy psoriasis secukinumab |
| title_short |
A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients. |
| title_full |
A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients. |
| title_fullStr |
A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients. |
| title_full_unstemmed |
A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients. |
| title_sort |
A prospective multicenter study assessing effectiveness and safety of secukinumab in a real-life setting in 158 patients. |
| dc.creator.none.fl_str_mv |
Ortiz Salvador JM Saneleuterio Temporal M Magdaleno Tapial J Manel VP Conrad PM Sahuquillo Torralba A Mateu-Puchades, Almudena Pitarch-Bort, Gerard Mari-Ruiz, Juan-Ignacio Mataix Díaz J Montesinos Villaescusa E Miralles-Botella, Julia Garcia-Fernandez, Laura Martorell Calatayud A Belinchon, I. Sánchez Carazo JL Pérez Ferriols A |
| author |
Ortiz Salvador JM |
| author_facet |
Ortiz Salvador JM Saneleuterio Temporal M Magdaleno Tapial J Manel VP Conrad PM Sahuquillo Torralba A Mateu-Puchades, Almudena Pitarch-Bort, Gerard Mari-Ruiz, Juan-Ignacio Mataix Díaz J Montesinos Villaescusa E Miralles-Botella, Julia Garcia-Fernandez, Laura Martorell Calatayud A Belinchon, I. Sánchez Carazo JL Pérez Ferriols A |
| author_role |
author |
| author2 |
Saneleuterio Temporal M Magdaleno Tapial J Manel VP Conrad PM Sahuquillo Torralba A Mateu-Puchades, Almudena Pitarch-Bort, Gerard Mari-Ruiz, Juan-Ignacio Mataix Díaz J Montesinos Villaescusa E Miralles-Botella, Julia Garcia-Fernandez, Laura Martorell Calatayud A Belinchon, I. Sánchez Carazo JL Pérez Ferriols A |
| author2_role |
author author author author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
IL-17 biologic therapy psoriasis secukinumab |
| topic |
IL-17 biologic therapy psoriasis secukinumab |
| description |
BACKGROUND: Secukinumab is a first-in-class interleukin 17A monoclonal antibody that has demonstrated an excellent safety and efficacy profile in phase 3 studies. OBJECTIVE: To evaluate the effectiveness of secukinumab in daily clinical practice and to understand the clinical and epidemiologic characteristics of patients treated with secukinumab in clinical settings. METHODS: In this multicenter prospective observational study, we recruited adult patients with moderate-to-severe plaque psoriasis from 12 hospitals in Spain during January-December 2016. These patients were treated with secukinumab and prospectively followed at 12-week intervals for 52 weeks. RESULTS: In total, 158 patients were recruited to the study. A Psoriasis Area and Severity Index (PASI) score improvement =75% over baseline (PASI-75) was achieved by 57%, 83.5%, 89%, and 78.5% of patients at weeks 4, 12, 24, and 52, respectively. PASI-90 was achieved in 27.8%, 62%, 64.6%, and 63.2% of patients at weeks 4, 12, 24, and 52, respectively; PASI-75 and PASI-90 responders were significantly more common among patients with a body mass index <30 kg/cm(2) and patients without previous biologic therapy failures. LIMITATIONS: Observational study. Time from onset of psoriasis was not evaluated. CONCLUSION: Secukinumab is a safe treatment with effectiveness rates similar to those found in its phase 3 studies. These rates endure up to a year from start of treatment. |
| publishDate |
2019 |
| dc.date.none.fl_str_mv |
2019 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://fisabio.portalinvestigacion.com/publicaciones/3341 |
| url |
https://fisabio.portalinvestigacion.com/publicaciones/3341 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
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openAccess |
| dc.publisher.none.fl_str_mv |
MOSBY-ELSEVIER |
| publisher.none.fl_str_mv |
MOSBY-ELSEVIER |
| dc.source.none.fl_str_mv |
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY ISSN: 01909622 ISSNe: 10976787 reponame:r-FISABIO. Repositorio Institucional de Producción Científica instname:Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO) |
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Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO) |
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r-FISABIO. Repositorio Institucional de Producción Científica |
| collection |
r-FISABIO. Repositorio Institucional de Producción Científica |
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|
| repository.mail.fl_str_mv |
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15,81155 |