Long-term Safety and Efficacy of Reslizumab in Patients with Eosinophilic Asthma

被引:109
|
作者
Murphy, Kevin [1 ]
Jacobs, Joshua [2 ]
Bjermer, Leif [3 ]
Fahrenholz, John M. [4 ]
Shalit, Yael [5 ]
Garin, Margaret [6 ]
Zangrilli, James [6 ]
Castro, Mario [7 ]
机构
[1] Boys Town Natl Res Hosp, Allergy Asthma & Pulm Res, Boys Town, NE USA
[2] Bay Area Inc, Allergy & Asthma Med Grp, Allergy & Asthma Clin Res, Walnut Creek, CA USA
[3] Skane Univ Hosp, Dept Resp Med & Allergol, Lund, Sweden
[4] Dept Vet Affairs Med Ctr, Sect Allergy & Immunol, Nashville, TN 37212 USA
[5] Teva Pharmaceut, Global Patient Safety & Pharmacovigilance, Petah Tiqwa, Israel
[6] Teva Pharmaceut, Global Resp R&D, Philadelphia, PA USA
[7] Washington Univ, Sch Med, Div Pulm & Crit Care Med, St Louis, MO USA
来源
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE | 2017年 / 5卷 / 06期
关键词
Reslizumab; Asthma; Eosinophil; Anti-IL-5; Long-term safety; Open-label extension study; HUMAN INTERLEUKIN-5; PERSISTENT ASTHMA; MEPOLIZUMAB; COUNTS; ANTIBODY; PHASE-3;
D O I
10.1016/j.jaip.2017.08.024
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: In placebo-controlled trials, reslizumab, an anti-IL-5 monoclonal antibody, significantly reduced asthma exacerbations and improved lung function and asthma control in patients with eosinophilic asthma. OBJECTIVE: This open-label extension study evaluated safety and efficacy of reslizumab for up to 24 months. METHODS: After participation in 1 of 3 placebo-controlled, phase III trials in moderate-to-severe eosinophilic asthma, patients received reslizumab 3.0 mg/kg intravenously every 4 weeks for up to 24 months. Adverse events (AEs), lung function, and patient-reported asthma control were evaluated. RESULTS: In the open-label extension, 1,051 patients received >= 1 reslizumab dose (480 reslizumab-naive, 571 reslizumabexperienced); median (range) exposure was 319 (36-840) and 343 (36-863) days in reslizumab-naive and reslizumab-experienced patients, respectively. Continuous exposure, including during the placebo-controlled studies, was >= 12 months for 740 patients and >= 24 months for 249 patients. The most common AEs were worsening of asthma and nasopharyngitis. Serious AEs affected 78 of 1,051 (7%) patients; 18 of 1,051 (2%) discontinued treatment because of AEs; and there were 3 deaths (all non-treatment-related). Fifteen adult patients (15 of 1,023; 1%) had malignancies of diverse tissue types. Reslizumab-experienced patients maintained improved lung function and asthma control; reslizumab-naive patients had improvements in these measures throughout open-label treatment. Blood eosinophil counts appeared to be returning to baseline after reslizumab discontinuation. CONCLUSIONS: In patients with moderate-to-severe eosinophilic asthma, intravenous reslizumab 3.0 mg/kg displays favorable long-term safety and sustained long-term efficacy. Initial improvements in lung function and asthma control were maintained for up to 2 years. These findings substantially add to our understanding of the long-term safety and efficacy of anti-IL-5 strategies. (C) 2017 The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.
引用
收藏
页码:1572 / +
页数:13
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