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Long-term Safety and Efficacy of Reslizumab in Patients with Eosinophilic Asthma
被引:108
|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
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.
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页码:1572 / +
页数:13
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