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Small, Prospective, Observational, Pilot Study in Patients with Severe Asthma after Discontinuation of Omalizumab Treatment
Omalizumab has demonstrated clinical efficacy in severe allergic asthma by reducing exacerbation rates and increasing quality of life. However, data concerning its sustained effect after treatment discontinuation are still needed. : This analysis was an observational pilot study (simple within-subje...
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Published in: | Clinical therapeutics 2018-11, Vol.40 (11), p.1942-1953 |
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creator | Krčmová, Irena Novosad, Jakub Malá, Eva Krejsek, Jan |
description | Omalizumab has demonstrated clinical efficacy in severe allergic asthma by reducing exacerbation rates and increasing quality of life. However, data concerning its sustained effect after treatment discontinuation are still needed.
: This analysis was an observational pilot study (simple within-subjects design) of 12 patients experiencing severe asthma, treated with omalizumab, for 1 year after treatment discontinuation. We prospectively analyzed clinical measurements (pulmonary functions, inhaled corticosteroid [ICS] doses, Asthma Control Test [ACT] scores, skin prick test [SPT] positivity, fraction of exhaled nitric oxide, and exacerbation rates) and laboratory test results (eosinophils and total immunoglobulin E levels) at the time of discontinuation and 6 and 12 months thereafter. Baseline data (before the treatment period; range, 11–61 months) were collected retrospectively. The treatment effect until discontinuation was calculated. To determine its persistence, repeated measures were compared with baseline levels and analyzed by using a general linear model for repeated measures or the Friedman ANOVA, and χ2 tests in case of normality assumption violation or frequencies. Post hoc analysis was applied by using a simple or repeated contrasts analysis or Wilcoxon signed rank test with Bonferroni correction.
: We proved a significant reduction in ICS doses and SPT reactivity and an increase in ACT score during the retrospective treatment phase. Moreover, persistence of these statistically significant effects was recorded 6 months after treatment discontinuation. ACT score and ICS doses (but not SPT reactivity) remained improved for 12 months after discontinuation of omalizumab treatment.
Omalizumab treatment exhibited sustained treatment benefit after its discontinuation for patients experiencing severe allergic asthma. |
doi_str_mv | 10.1016/j.clinthera.2018.09.004 |
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: This analysis was an observational pilot study (simple within-subjects design) of 12 patients experiencing severe asthma, treated with omalizumab, for 1 year after treatment discontinuation. We prospectively analyzed clinical measurements (pulmonary functions, inhaled corticosteroid [ICS] doses, Asthma Control Test [ACT] scores, skin prick test [SPT] positivity, fraction of exhaled nitric oxide, and exacerbation rates) and laboratory test results (eosinophils and total immunoglobulin E levels) at the time of discontinuation and 6 and 12 months thereafter. Baseline data (before the treatment period; range, 11–61 months) were collected retrospectively. The treatment effect until discontinuation was calculated. To determine its persistence, repeated measures were compared with baseline levels and analyzed by using a general linear model for repeated measures or the Friedman ANOVA, and χ2 tests in case of normality assumption violation or frequencies. Post hoc analysis was applied by using a simple or repeated contrasts analysis or Wilcoxon signed rank test with Bonferroni correction.
: We proved a significant reduction in ICS doses and SPT reactivity and an increase in ACT score during the retrospective treatment phase. Moreover, persistence of these statistically significant effects was recorded 6 months after treatment discontinuation. ACT score and ICS doses (but not SPT reactivity) remained improved for 12 months after discontinuation of omalizumab treatment.
Omalizumab treatment exhibited sustained treatment benefit after its discontinuation for patients experiencing severe allergic asthma.</description><identifier>ISSN: 0149-2918</identifier><identifier>EISSN: 1879-114X</identifier><identifier>DOI: 10.1016/j.clinthera.2018.09.004</identifier><identifier>PMID: 30391022</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Allergies ; Asthma ; Asthma Control Test ; Clinical trials ; Corticosteroids ; Data collection ; FDA approval ; Immunoglobulin E ; Immunotherapy ; Inflammation ; inhaled corticosteroids ; Laboratories ; Laboratory tests ; Leukocytes (eosinophilic) ; Monoclonal antibodies ; Nitric oxide ; Normality ; omalizumab ; Patients ; Pulmonary functions ; Quality of life ; Rank tests ; severe asthma ; skin prick test ; Skin tests ; Statistical analysis ; Variance analysis</subject><ispartof>Clinical therapeutics, 2018-11, Vol.40 (11), p.1942-1953</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Nov 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c399t-b6db3835b273f0df2d7e5c763594f6d295bf5d0c7eeeefa8c81f77eb3bfda7793</citedby><cites>FETCH-LOGICAL-c399t-b6db3835b273f0df2d7e5c763594f6d295bf5d0c7eeeefa8c81f77eb3bfda7793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30391022$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krčmová, Irena</creatorcontrib><creatorcontrib>Novosad, Jakub</creatorcontrib><creatorcontrib>Malá, Eva</creatorcontrib><creatorcontrib>Krejsek, Jan</creatorcontrib><title>Small, Prospective, Observational, Pilot Study in Patients with Severe Asthma after Discontinuation of Omalizumab Treatment</title><title>Clinical therapeutics</title><addtitle>Clin Ther</addtitle><description>Omalizumab has demonstrated clinical efficacy in severe allergic asthma by reducing exacerbation rates and increasing quality of life. However, data concerning its sustained effect after treatment discontinuation are still needed.
: This analysis was an observational pilot study (simple within-subjects design) of 12 patients experiencing severe asthma, treated with omalizumab, for 1 year after treatment discontinuation. We prospectively analyzed clinical measurements (pulmonary functions, inhaled corticosteroid [ICS] doses, Asthma Control Test [ACT] scores, skin prick test [SPT] positivity, fraction of exhaled nitric oxide, and exacerbation rates) and laboratory test results (eosinophils and total immunoglobulin E levels) at the time of discontinuation and 6 and 12 months thereafter. Baseline data (before the treatment period; range, 11–61 months) were collected retrospectively. The treatment effect until discontinuation was calculated. To determine its persistence, repeated measures were compared with baseline levels and analyzed by using a general linear model for repeated measures or the Friedman ANOVA, and χ2 tests in case of normality assumption violation or frequencies. Post hoc analysis was applied by using a simple or repeated contrasts analysis or Wilcoxon signed rank test with Bonferroni correction.
: We proved a significant reduction in ICS doses and SPT reactivity and an increase in ACT score during the retrospective treatment phase. Moreover, persistence of these statistically significant effects was recorded 6 months after treatment discontinuation. ACT score and ICS doses (but not SPT reactivity) remained improved for 12 months after discontinuation of omalizumab treatment.
Omalizumab treatment exhibited sustained treatment benefit after its discontinuation for patients experiencing severe allergic asthma.</description><subject>Allergies</subject><subject>Asthma</subject><subject>Asthma Control Test</subject><subject>Clinical trials</subject><subject>Corticosteroids</subject><subject>Data collection</subject><subject>FDA approval</subject><subject>Immunoglobulin E</subject><subject>Immunotherapy</subject><subject>Inflammation</subject><subject>inhaled corticosteroids</subject><subject>Laboratories</subject><subject>Laboratory tests</subject><subject>Leukocytes (eosinophilic)</subject><subject>Monoclonal antibodies</subject><subject>Nitric oxide</subject><subject>Normality</subject><subject>omalizumab</subject><subject>Patients</subject><subject>Pulmonary functions</subject><subject>Quality of life</subject><subject>Rank tests</subject><subject>severe asthma</subject><subject>skin prick test</subject><subject>Skin tests</subject><subject>Statistical analysis</subject><subject>Variance analysis</subject><issn>0149-2918</issn><issn>1879-114X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkUtvEzEUhS0EoiHwF8ASGxadwY-ZeLyMylOqlEopEjvLY18rjmbGwfYEFf48TlO6YIM3tnS_e451DkJvKKkpoav3-9oMfso7iLpmhHY1kTUhzRO0oJ2QFaXN96doQWgjKyZpd4FepLQnhHDZsufogpcHJYwt0O_tqIfhEt_EkA5gsj_CJd70CeJRZx8mfZr5IWS8zbO9w37CN2UAU074p887vIUjRMDrlHejxtpliPiDTyZM2U_zvQYODm-Kjf81j7rHtxF0HovCS_TM6SHBq4d7ib59-nh79aW63nz-erW-rgyXMlf9yva8423PBHfEOmYFtEaseCsbt7JMtr1rLTECynG6Mx11QkDPe2e1EJIv0buz7iGGHzOkrMbyQRgGPUGYk2KUE9LKVnQFffsPug9zLCncUw1rJSnGSyTOlCmppQhOHaIfdbxTlKhTP2qvHvtRp34Ukar0UzZfP-jP_Qj2ce9vIQVYnwEogRw9RJVMSduA9bHUo2zw_zX5A1PbqAU</recordid><startdate>201811</startdate><enddate>201811</enddate><creator>Krčmová, Irena</creator><creator>Novosad, Jakub</creator><creator>Malá, Eva</creator><creator>Krejsek, Jan</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>201811</creationdate><title>Small, Prospective, Observational, Pilot Study in Patients with Severe Asthma after Discontinuation of Omalizumab Treatment</title><author>Krčmová, Irena ; Novosad, Jakub ; Malá, Eva ; Krejsek, Jan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c399t-b6db3835b273f0df2d7e5c763594f6d295bf5d0c7eeeefa8c81f77eb3bfda7793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Allergies</topic><topic>Asthma</topic><topic>Asthma Control Test</topic><topic>Clinical trials</topic><topic>Corticosteroids</topic><topic>Data collection</topic><topic>FDA approval</topic><topic>Immunoglobulin E</topic><topic>Immunotherapy</topic><topic>Inflammation</topic><topic>inhaled corticosteroids</topic><topic>Laboratories</topic><topic>Laboratory tests</topic><topic>Leukocytes (eosinophilic)</topic><topic>Monoclonal antibodies</topic><topic>Nitric oxide</topic><topic>Normality</topic><topic>omalizumab</topic><topic>Patients</topic><topic>Pulmonary functions</topic><topic>Quality of life</topic><topic>Rank tests</topic><topic>severe asthma</topic><topic>skin prick test</topic><topic>Skin tests</topic><topic>Statistical analysis</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krčmová, Irena</creatorcontrib><creatorcontrib>Novosad, Jakub</creatorcontrib><creatorcontrib>Malá, Eva</creatorcontrib><creatorcontrib>Krejsek, Jan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krčmová, Irena</au><au>Novosad, Jakub</au><au>Malá, Eva</au><au>Krejsek, Jan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Small, Prospective, Observational, Pilot Study in Patients with Severe Asthma after Discontinuation of Omalizumab Treatment</atitle><jtitle>Clinical therapeutics</jtitle><addtitle>Clin Ther</addtitle><date>2018-11</date><risdate>2018</risdate><volume>40</volume><issue>11</issue><spage>1942</spage><epage>1953</epage><pages>1942-1953</pages><issn>0149-2918</issn><eissn>1879-114X</eissn><abstract>Omalizumab has demonstrated clinical efficacy in severe allergic asthma by reducing exacerbation rates and increasing quality of life. However, data concerning its sustained effect after treatment discontinuation are still needed.
: This analysis was an observational pilot study (simple within-subjects design) of 12 patients experiencing severe asthma, treated with omalizumab, for 1 year after treatment discontinuation. We prospectively analyzed clinical measurements (pulmonary functions, inhaled corticosteroid [ICS] doses, Asthma Control Test [ACT] scores, skin prick test [SPT] positivity, fraction of exhaled nitric oxide, and exacerbation rates) and laboratory test results (eosinophils and total immunoglobulin E levels) at the time of discontinuation and 6 and 12 months thereafter. Baseline data (before the treatment period; range, 11–61 months) were collected retrospectively. The treatment effect until discontinuation was calculated. To determine its persistence, repeated measures were compared with baseline levels and analyzed by using a general linear model for repeated measures or the Friedman ANOVA, and χ2 tests in case of normality assumption violation or frequencies. Post hoc analysis was applied by using a simple or repeated contrasts analysis or Wilcoxon signed rank test with Bonferroni correction.
: We proved a significant reduction in ICS doses and SPT reactivity and an increase in ACT score during the retrospective treatment phase. Moreover, persistence of these statistically significant effects was recorded 6 months after treatment discontinuation. ACT score and ICS doses (but not SPT reactivity) remained improved for 12 months after discontinuation of omalizumab treatment.
Omalizumab treatment exhibited sustained treatment benefit after its discontinuation for patients experiencing severe allergic asthma.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30391022</pmid><doi>10.1016/j.clinthera.2018.09.004</doi><tpages>12</tpages></addata></record> |
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subjects | Allergies Asthma Asthma Control Test Clinical trials Corticosteroids Data collection FDA approval Immunoglobulin E Immunotherapy Inflammation inhaled corticosteroids Laboratories Laboratory tests Leukocytes (eosinophilic) Monoclonal antibodies Nitric oxide Normality omalizumab Patients Pulmonary functions Quality of life Rank tests severe asthma skin prick test Skin tests Statistical analysis Variance analysis |
title | Small, Prospective, Observational, Pilot Study in Patients with Severe Asthma after Discontinuation of Omalizumab Treatment |
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