Bimekizumab in the Treatment of Plaque Psoriasis
Psoriasis is a chronic systemic inflammatory disease that significatively impairs patients' quality of life. Biological treatments are highly effective and safe and have led to breakthroughs in the management of patients with moderate-to-severe psoriasis. However, therapeutic response can be un...
| Autores: | , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2023 |
| País: | España |
| Institución: | Universitat Autònoma de Barcelona |
| Repositorio: | Dipòsit Digital de Documents de la UAB |
| Idioma: | inglés |
| OAI Identifier: | oai:ddd.uab.cat:303475 |
| Acceso en línea: | https://ddd.uab.cat/record/303475 https://dx.doi.org/urn:doi:10.2147/PPA.S350760 |
| Access Level: | acceso abierto |
| Palabra clave: | Bimekizumab Biological therapy Interleukin-17 Patient compliance Patient selection Psoriasis |
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Bimekizumab in the Treatment of Plaque PsoriasisFocus on Patient Selection and PerspectivesCamiña-Conforto, Gemma|||0009-0008-2183-9397Mateu Arrom, Laura|||0000-0001-8522-4748López Ferrer, Anna|||0000-0002-2121-963XPuig Sanz, Lluís|||0000-0001-6083-0952BimekizumabBiological therapyInterleukin-17Patient compliancePatient selectionPsoriasisPsoriasis is a chronic systemic inflammatory disease that significatively impairs patients' quality of life. Biological treatments are highly effective and safe and have led to breakthroughs in the management of patients with moderate-to-severe psoriasis. However, therapeutic response can be unsatisfactory or lost with time, leading to discontinuation of treatment. Bimekizumab is a humanized monoclonal antibody that specifically inhibits both interleukin (IL)-17A and IL-17F. The efficacy and safety of bimekizumab in moderate-to-severe plaque psoriasis has been demonstrated in Phase 2 and Phase 3 clinical trials. Bimekizumab may offer some advantages over other biological treatments, making it especially indicated for certain patients. This narrative review aims to summarize the latest published evidence on the use of bimekizumab for the treatment of moderate-severe plaque psoriasis, focusing on patient selection and therapeutic perspectives. Bimekizumab has been shown to be more efficacious than adalimumab, secukinumab and ustekinumab in clinical trials, with high estimated probabilities of achieving complete (approximately 60%) or almost complete clearance (approximately 85%) of psoriasis at weeks 10-16, and a good safety profile. Response to bimekizumab is usually fast and maintained in the long term for both biologic-naive patients and those resistant to previous biologic treatments. The usual maintenance dose of 320 mg every 8 weeks makes bimekizumab especially convenient for non-compliant patients. Moreover, the efficacy and safety of bimekizumab have also been demonstrated in psoriasis affecting challenging-to-treat areas, psoriatic arthritis and hidradenitis suppurativa. In conclusion, dual inhibition of IL-17A and IL-17F with bimekizumab is a good therapeutic option for moderate-to-severe psoriasis.Universitat Autònoma de Barcelona 22023-01-0120232023-01-01Article de revisióhttp://purl.org/coar/resource_type/c_dcae04bcVoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/303475https://dx.doi.org/urn:doi:10.2147/PPA.S350760reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengopen accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original.https://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:3034752026-06-06T12:50:31Z |
| dc.title.none.fl_str_mv |
Bimekizumab in the Treatment of Plaque Psoriasis Focus on Patient Selection and Perspectives |
| title |
Bimekizumab in the Treatment of Plaque Psoriasis |
| spellingShingle |
Bimekizumab in the Treatment of Plaque Psoriasis Camiña-Conforto, Gemma|||0009-0008-2183-9397 Bimekizumab Biological therapy Interleukin-17 Patient compliance Patient selection Psoriasis |
| title_short |
Bimekizumab in the Treatment of Plaque Psoriasis |
| title_full |
Bimekizumab in the Treatment of Plaque Psoriasis |
| title_fullStr |
Bimekizumab in the Treatment of Plaque Psoriasis |
| title_full_unstemmed |
Bimekizumab in the Treatment of Plaque Psoriasis |
| title_sort |
Bimekizumab in the Treatment of Plaque Psoriasis |
| dc.creator.none.fl_str_mv |
Camiña-Conforto, Gemma|||0009-0008-2183-9397 Mateu Arrom, Laura|||0000-0001-8522-4748 López Ferrer, Anna|||0000-0002-2121-963X Puig Sanz, Lluís|||0000-0001-6083-0952 |
| author |
Camiña-Conforto, Gemma|||0009-0008-2183-9397 |
| author_facet |
Camiña-Conforto, Gemma|||0009-0008-2183-9397 Mateu Arrom, Laura|||0000-0001-8522-4748 López Ferrer, Anna|||0000-0002-2121-963X Puig Sanz, Lluís|||0000-0001-6083-0952 |
| author_role |
author |
| author2 |
Mateu Arrom, Laura|||0000-0001-8522-4748 López Ferrer, Anna|||0000-0002-2121-963X Puig Sanz, Lluís|||0000-0001-6083-0952 |
| author2_role |
author author author |
| dc.contributor.none.fl_str_mv |
Universitat Autònoma de Barcelona |
| dc.subject.none.fl_str_mv |
Bimekizumab Biological therapy Interleukin-17 Patient compliance Patient selection Psoriasis |
| topic |
Bimekizumab Biological therapy Interleukin-17 Patient compliance Patient selection Psoriasis |
| description |
Psoriasis is a chronic systemic inflammatory disease that significatively impairs patients' quality of life. Biological treatments are highly effective and safe and have led to breakthroughs in the management of patients with moderate-to-severe psoriasis. However, therapeutic response can be unsatisfactory or lost with time, leading to discontinuation of treatment. Bimekizumab is a humanized monoclonal antibody that specifically inhibits both interleukin (IL)-17A and IL-17F. The efficacy and safety of bimekizumab in moderate-to-severe plaque psoriasis has been demonstrated in Phase 2 and Phase 3 clinical trials. Bimekizumab may offer some advantages over other biological treatments, making it especially indicated for certain patients. This narrative review aims to summarize the latest published evidence on the use of bimekizumab for the treatment of moderate-severe plaque psoriasis, focusing on patient selection and therapeutic perspectives. Bimekizumab has been shown to be more efficacious than adalimumab, secukinumab and ustekinumab in clinical trials, with high estimated probabilities of achieving complete (approximately 60%) or almost complete clearance (approximately 85%) of psoriasis at weeks 10-16, and a good safety profile. Response to bimekizumab is usually fast and maintained in the long term for both biologic-naive patients and those resistant to previous biologic treatments. The usual maintenance dose of 320 mg every 8 weeks makes bimekizumab especially convenient for non-compliant patients. Moreover, the efficacy and safety of bimekizumab have also been demonstrated in psoriasis affecting challenging-to-treat areas, psoriatic arthritis and hidradenitis suppurativa. In conclusion, dual inhibition of IL-17A and IL-17F with bimekizumab is a good therapeutic option for moderate-to-severe psoriasis. |
| publishDate |
2023 |
| dc.date.none.fl_str_mv |
2 2023-01-01 2023 2023-01-01 |
| dc.type.none.fl_str_mv |
Article de revisió http://purl.org/coar/resource_type/c_dcae04bc VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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article |
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https://ddd.uab.cat/record/303475 https://dx.doi.org/urn:doi:10.2147/PPA.S350760 |
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https://ddd.uab.cat/record/303475 https://dx.doi.org/urn:doi:10.2147/PPA.S350760 |
| dc.language.none.fl_str_mv |
Inglés eng |
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Inglés |
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eng |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by-nc/4.0/ |
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info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by-nc/4.0/ |
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openAccess |
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application/pdf |
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