Reslizumab for Poorly Controlled, Eosinophilic Asthma: A Randomized, Placebo-controlled Study
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- Mario Castro
- Washington University School of Medicine, St. Louis, Missouri
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- Sameer Mathur
- University of Wisconsin, Madison, Madison, Wisconsin
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- Frederick Hargreave
- McMaster University, Hamilton, Ontario, Canada
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- Louis-Philippe Boulet
- Institut Universitaire de Cardiologie et de Pneumologie de Québec, Québec, Canada
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- Fang Xie
- Cephalon, Inc., Frazer, Pennsylvania; and
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- James Young
- United BioSource Corporation, Ann Arbor, Michigan
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- H. Jeffrey Wilkins
- Cephalon, Inc., Frazer, Pennsylvania; and
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- Timothy Henkel
- Cephalon, Inc., Frazer, Pennsylvania; and
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- Parameswaran Nair
- McMaster University, Hamilton, Ontario, Canada
書誌事項
- 公開日
- 2011-11
- 権利情報
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- https://academic.oup.com/pages/standard-publication-reuse-rights
- DOI
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- 10.1164/rccm.201103-0396oc
- 公開者
- Oxford University Press (OUP)
この論文をさがす
説明
<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Rationale</jats:title> <jats:p>Eosinophilic asthma is a phenotype of asthma characterized by the persistence of eosinophils in the airways. IL-5 is involved in the activation and survival of eosinophils.</jats:p> </jats:sec> <jats:sec> <jats:title>Objectives</jats:title> <jats:p>To evaluate the effect of the antibody to IL-5, reslizumab, in patients with eosinophilic asthma that is poorly controlled with high-dose inhaled corticosteroid.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>Patients were randomly assigned to receive infusions of reslizumab at 3.0 mg/kg (n = 53) or placebo (n = 53) at baseline and at Weeks 4, 8, and 12, with stratification by baseline Asthma Control Questionnaire (ACQ) score less than or equal to 2 or greater than 2. The primary efficacy measure was the difference between the reslizumab and placebo groups in the change in ACQ score from baseline to end of therapy (Week 15 or early withdrawal).</jats:p> </jats:sec> <jats:sec> <jats:title>Measurements and Main Results</jats:title> <jats:p>Mean changes from baseline to end of therapy in ACQ score were –0.7 in the reslizumab group and –0.3 in the placebo group (P = 0.054) and in FEV1 were 0.18 and –0.08 L, respectively (P = 0.002). In those patients with nasal polyps, the changes in ACQ score were –1.0 and –0.1, respectively (P = 0.012). Median percentage reductions from baseline in sputum eosinophils were 95.4 and 38.7%, respectively (P = 0.007). Eight percent of patients in the reslizumab group and 19% of patients in the placebo group had an asthma exacerbation (P = 0.083). The most common adverse events with reslizumab were nasopharyngitis, fatigue, and pharyngolaryngeal pain.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>Patients receiving reslizumab showed significantly greater reductions in sputum eosinophils, improvements in airway function, and a trend toward greater asthma control than those receiving placebo. Reslizumab was generally well tolerated.</jats:p> </jats:sec>
収録刊行物
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- American Journal of Respiratory and Critical Care Medicine
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American Journal of Respiratory and Critical Care Medicine 184 (10), 1125-1132, 2011-11
Oxford University Press (OUP)