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Approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence

BACKGROUND: Efalizumab is a humanised recombinant monoclonal IgG1 antibody for the treatment of moderate-to-severe plaque psoriasis. When treatment discontinuation is necessary, however, some patients may experience inflammatory recurrence of the disease, which can progress to rebound if untreated....

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Autores principales: Papp, Kim A, Toth, Darryl, Rosoph, Les
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636659/
https://www.ncbi.nlm.nih.gov/pubmed/17067371
http://dx.doi.org/10.1186/1471-5945-6-9
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author Papp, Kim A
Toth, Darryl
Rosoph, Les
author_facet Papp, Kim A
Toth, Darryl
Rosoph, Les
author_sort Papp, Kim A
collection PubMed
description BACKGROUND: Efalizumab is a humanised recombinant monoclonal IgG1 antibody for the treatment of moderate-to-severe plaque psoriasis. When treatment discontinuation is necessary, however, some patients may experience inflammatory recurrence of the disease, which can progress to rebound if untreated. This analysis evaluated approaches for managing inflammatory recurrence after discontinuation of efalizumab. METHODS: An open-label, multicentre, investigational study was performed in 41 patients with moderate-to-severe plaque psoriasis who had recently completed clinical studies with efalizumab and had developed signs of inflammatory recurrence following abrupt cessation of treatment. Patients were assigned by the attending physicians to receive one of five standardised alternative systemic psoriasis treatment regimens for 12 weeks. Efficacy of the different therapy options was assessed using the physician's global assessment (PGA) of change over time. RESULTS: More favourable PGA responses were observed in patients changing to cyclosporin (PGA of 'good', 'excellent' or 'cleared': 7/10 patients, 70.0%) or methotrexate (9/20, 45.0%), compared with those receiving systemic corticosteroids (2/8, 25.0%), retinoids (0/1, 0.0%) or combined corticosteroids plus methotrexate (0/2, 0.0%). While the majority (77.8%) of patients showed inflammatory morphology at baseline, following 12 weeks of the alternative therapies the overall prevalence of inflammatory disease was decreased to 19.2%. CONCLUSION: Inflammatory recurrence after discontinuation of efalizumab therapy is a manageable event, with a number of therapies and approaches available to physicians, including short courses of cyclosporin or methotrexate.
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spelling pubmed-16366592006-11-16 Approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence Papp, Kim A Toth, Darryl Rosoph, Les BMC Dermatol Research Article BACKGROUND: Efalizumab is a humanised recombinant monoclonal IgG1 antibody for the treatment of moderate-to-severe plaque psoriasis. When treatment discontinuation is necessary, however, some patients may experience inflammatory recurrence of the disease, which can progress to rebound if untreated. This analysis evaluated approaches for managing inflammatory recurrence after discontinuation of efalizumab. METHODS: An open-label, multicentre, investigational study was performed in 41 patients with moderate-to-severe plaque psoriasis who had recently completed clinical studies with efalizumab and had developed signs of inflammatory recurrence following abrupt cessation of treatment. Patients were assigned by the attending physicians to receive one of five standardised alternative systemic psoriasis treatment regimens for 12 weeks. Efficacy of the different therapy options was assessed using the physician's global assessment (PGA) of change over time. RESULTS: More favourable PGA responses were observed in patients changing to cyclosporin (PGA of 'good', 'excellent' or 'cleared': 7/10 patients, 70.0%) or methotrexate (9/20, 45.0%), compared with those receiving systemic corticosteroids (2/8, 25.0%), retinoids (0/1, 0.0%) or combined corticosteroids plus methotrexate (0/2, 0.0%). While the majority (77.8%) of patients showed inflammatory morphology at baseline, following 12 weeks of the alternative therapies the overall prevalence of inflammatory disease was decreased to 19.2%. CONCLUSION: Inflammatory recurrence after discontinuation of efalizumab therapy is a manageable event, with a number of therapies and approaches available to physicians, including short courses of cyclosporin or methotrexate. BioMed Central 2006-10-26 /pmc/articles/PMC1636659/ /pubmed/17067371 http://dx.doi.org/10.1186/1471-5945-6-9 Text en Copyright © 2006 Papp et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Papp, Kim A
Toth, Darryl
Rosoph, Les
Approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence
title Approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence
title_full Approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence
title_fullStr Approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence
title_full_unstemmed Approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence
title_short Approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence
title_sort approaches to discontinuing efalizumab: an open-label study of therapies for managing inflammatory recurrence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1636659/
https://www.ncbi.nlm.nih.gov/pubmed/17067371
http://dx.doi.org/10.1186/1471-5945-6-9
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