Efficacy and safety of sublingual immunotherapy with grass allergen tablets for seasonal allergic rhinoconjunctivitis

被引:361
作者
Dahl, Ronald
Kapp, Alexander
Colombo, Giselda
deMonchy, Jan G. R.
Rak, Sabina
Emminger, Waltraud
Rivas, Montserrat Fernandez
Ribel, Mette
Durham, Stephen R.
机构
[1] Royal Brompton Hosp,Imperial Coll, MRC & Asthma UK Ctr Allerg Mech Asthma, Allergy & Clin Immunol Sect, Natl Heart & Lung Inst, London SW3 6LY, England
[2] Aarhus Univ Hosp, Dept Resp Dis, DK-8000 Aarhus, Denmark
[3] Hannover Med Sch, Dept Dermatol & Allergol, Hannover, Germany
[4] Osped San Raffaele, I-20127 Milan, Italy
[5] Univ Groningen, Div Allergol, NL-9700 AB Groningen, Netherlands
[6] Sahlgrens Univ Hosp, Sect Allergy, Gothenburg, Sweden
[7] Allergie Ambulatorium Rennweg, Vienna, Austria
[8] Fdn Hosp Alcorcon, Madrid, Spain
[9] ALK Abello AS, Grp Clin Dev, Horsholm, Denmark
基金
英国医学研究理事会;
关键词
allergy; asthma; grass pollen; immunotherapy; sublingual; rhinoconjunctivitis; tablet-based; double-blind; placebo-controlled; Phleum pratense;
D O I
10.1016/j.jaci.2006.05.003
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Allergen immunotherapy (desensitization) by injection is effective for seasonal allergic rhinitis and has been shown to induce long-term disease remission. The sublingual route also has potential, although definitive evidence from large randomized controlled trials has been lacking. Objective: The aim was to confirm the efficacy of a rapidly dissolving grass allergen tablet (GRAZAX, ALK-Abello, Horsholm, Denmark) compared with placebo in patients with seasonal rhinoconjunctivitis. Methods: A longitudinal, double-blind, placebo-controlled, parallel-group study that included 51 centers from 8 countries. Subjects were randomized (1:1) to receive a grass allergen tablet or placebo once daily. A total of 634 subjects with a history of grass pollen-induced rhinoconjunctivitis for at least 2 years and confirmation of IgE sensitivity (positive skin prick test and serum-specific IgE) were included in the study. Subjects commenced treatment at least 16 weeks before the grass pollen season, and treatment was continued throughout the entire season. Results: The primary efficacy analysis showed a reduction of 30% in rhinoconjunctivitis symptom score (P < .0001) and a reduction of 38% in rhinoconjunctivitis medication score (P < .0001) compared with placebo. Side effects mainly comprised mild itching and swelling in the mouth that was in general well tolerated and led to treatment withdrawal in less than 4% of participants. There were no serious local side effects and no severe systemic adverse events. Conclusion: Sublingual immunotherapy with grass allergen tablets was effective in grass pollen-induced rhinoconjunctivitis. The tablet was well tolerated with minor local side effects. Clinical implications: The grass allergen tablet represents a safe alternative to injection immunotherapy suitable for home use.
引用
收藏
页码:434 / 440
页数:7
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