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Omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria

BACKGROUND: Chronic spontaneous/idiopathic urticaria (CSU/CIU) has substantial detrimental effects on health‐related quality of life (HRQoL) with an effect comparable to or worse than many other skin diseases. OBJECTIVE: To assess the effect of omalizumab on CSU patients' HRQoL, measured by the...

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Autores principales: Finlay, A.Y., Kaplan, A.P., Beck, L.A., Antonova, E.N., Balp, M.‐M., Zazzali, J., Khalil, S., Maurer, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697571/
https://www.ncbi.nlm.nih.gov/pubmed/28573683
http://dx.doi.org/10.1111/jdv.14384
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author Finlay, A.Y.
Kaplan, A.P.
Beck, L.A.
Antonova, E.N.
Balp, M.‐M.
Zazzali, J.
Khalil, S.
Maurer, M.
author_facet Finlay, A.Y.
Kaplan, A.P.
Beck, L.A.
Antonova, E.N.
Balp, M.‐M.
Zazzali, J.
Khalil, S.
Maurer, M.
author_sort Finlay, A.Y.
collection PubMed
description BACKGROUND: Chronic spontaneous/idiopathic urticaria (CSU/CIU) has substantial detrimental effects on health‐related quality of life (HRQoL) with an effect comparable to or worse than many other skin diseases. OBJECTIVE: To assess the effect of omalizumab on CSU patients' HRQoL, measured by the Dermatology Life Quality Index (DLQI) in three phase III studies ASTERIA I, ASTERIA II and GLACIAL. METHODS: A post hoc analysis examined changes in DLQI scores, distribution of patients across DLQI bands and the proportion reaching minimal clinically important difference (MCID) following omalizumab vs. placebo. RESULTS: Omalizumab 300 mg significantly improved total DLQI scores vs. placebo, with a mean decrease from baseline to week 12 of −10.3 vs. −6.1 (P < 0.0001) in ASTERIA I, −10.2 vs. −6.1 (P = 0.0004) in ASTERIA II and −9.7 vs. −5.1 (P < 0.0001) in GLACIAL. A significant shift from high disease impact on life at baseline towards less impact at week 12 was seen with omalizumab 300 mg vs. placebo (P < 0.001; all studies). The proportion of patients where change in mean total DLQI score from baseline to week 12 reached an MCID of ≥4 was 74.1%, 76.0% and 77.2% in ASTERIA I, II and GLACIAL, respectively (P < 0.01; all studies). LIMITATIONS: Maximum duration of omalizumab treatment was 24 weeks. CONCLUSION: This additional analysis assessed the impact of CSU and benefit of treatment with omalizumab by exploring different facets of DLQI data by treatment arm at multiple assessment points. The original aspects of analysis included applying the concept of the recently validated score for the MCID of the DLQI, changes in DLQI domain scores and in the distribution of subjects based on validated total DLQI score bands. It showed consistently that omalizumab provides significant and clinically relevant improvements in many aspects of HRQoL that are important to patients with CSU. These results contribute to a better understanding of the impact of CSU and its treatment on patients and can support clinical decision‐making in routine medical practice.
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spelling pubmed-56975712017-11-28 Omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria Finlay, A.Y. Kaplan, A.P. Beck, L.A. Antonova, E.N. Balp, M.‐M. Zazzali, J. Khalil, S. Maurer, M. J Eur Acad Dermatol Venereol Original Articles and Short Reports BACKGROUND: Chronic spontaneous/idiopathic urticaria (CSU/CIU) has substantial detrimental effects on health‐related quality of life (HRQoL) with an effect comparable to or worse than many other skin diseases. OBJECTIVE: To assess the effect of omalizumab on CSU patients' HRQoL, measured by the Dermatology Life Quality Index (DLQI) in three phase III studies ASTERIA I, ASTERIA II and GLACIAL. METHODS: A post hoc analysis examined changes in DLQI scores, distribution of patients across DLQI bands and the proportion reaching minimal clinically important difference (MCID) following omalizumab vs. placebo. RESULTS: Omalizumab 300 mg significantly improved total DLQI scores vs. placebo, with a mean decrease from baseline to week 12 of −10.3 vs. −6.1 (P < 0.0001) in ASTERIA I, −10.2 vs. −6.1 (P = 0.0004) in ASTERIA II and −9.7 vs. −5.1 (P < 0.0001) in GLACIAL. A significant shift from high disease impact on life at baseline towards less impact at week 12 was seen with omalizumab 300 mg vs. placebo (P < 0.001; all studies). The proportion of patients where change in mean total DLQI score from baseline to week 12 reached an MCID of ≥4 was 74.1%, 76.0% and 77.2% in ASTERIA I, II and GLACIAL, respectively (P < 0.01; all studies). LIMITATIONS: Maximum duration of omalizumab treatment was 24 weeks. CONCLUSION: This additional analysis assessed the impact of CSU and benefit of treatment with omalizumab by exploring different facets of DLQI data by treatment arm at multiple assessment points. The original aspects of analysis included applying the concept of the recently validated score for the MCID of the DLQI, changes in DLQI domain scores and in the distribution of subjects based on validated total DLQI score bands. It showed consistently that omalizumab provides significant and clinically relevant improvements in many aspects of HRQoL that are important to patients with CSU. These results contribute to a better understanding of the impact of CSU and its treatment on patients and can support clinical decision‐making in routine medical practice. John Wiley and Sons Inc. 2017-07-19 2017-10 /pmc/articles/PMC5697571/ /pubmed/28573683 http://dx.doi.org/10.1111/jdv.14384 Text en © 2017 The Authors. Journal of the European Academy of Dermatology and Venereology published by John Wiley & Sons Ltd on behalf of European Academy of Dermatology and Venereology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles and Short Reports
Finlay, A.Y.
Kaplan, A.P.
Beck, L.A.
Antonova, E.N.
Balp, M.‐M.
Zazzali, J.
Khalil, S.
Maurer, M.
Omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria
title Omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria
title_full Omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria
title_fullStr Omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria
title_full_unstemmed Omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria
title_short Omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria
title_sort omalizumab substantially improves dermatology‐related quality of life in patients with chronic spontaneous urticaria
topic Original Articles and Short Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5697571/
https://www.ncbi.nlm.nih.gov/pubmed/28573683
http://dx.doi.org/10.1111/jdv.14384
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