Sustained 3-year efficacy of pre- and coseasonal 5-grass-pollen sublingual immunotherapy tablets in patients with grass pollen-induced rhinoconjunctivitis

被引:135
|
作者
Didier, Alain [1 ]
Worm, Margitta [3 ]
Horak, Friedrich [4 ]
Sussman, Gordon [5 ]
de Beaumont, Olivier [6 ]
Le Gall, Martine [6 ]
Melac, Michel [6 ]
Malling, Hans-Jorgen [2 ]
机构
[1] Rangueil Larrey Hosp, Dept Resp Dis, F-31059 Toulouse 9, France
[2] Natl Univ Hosp, Copenhagen, Denmark
[3] Univ Med Berlin, Ctr Allerg, Charite, Berlin, Germany
[4] Allergy Ctr Vienna W, Vienna, Austria
[5] Univ Toronto, Toronto, ON M5S 1A1, Canada
[6] Stallergenes SA, Antony, France
关键词
Rhinoconjunctivitis; sublingual immunotherapy; grass pollen; allergen; pre- and coseasonal treatment; ALLERGIC RHINITIS; ORGANIZATION; SAFETY;
D O I
10.1016/j.jaci.2011.06.022
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Seasonal allergic rhinoconjunctivitis affects millions of persons. The efficacy of allergen sublingual immunotherapy (SLIT) was demonstrated in previous short-term studies. Objectives: We sought to evaluate the sustained efficacy of 2 dosing regimens of a pre- and coseasonal treatment with 300 IR (index of reactivity) 5-grass-pollen SLIT tablets (Oralair) compared with placebo assessed by using the average adjusted symptom score (AAdSS) at season 3 in adults with grass pollen-induced rhinoconjunctivitis. Methods: Six hundred thirty-three patients were treated for either 2 or 4 months before and then during the grass pollen season with active or placebo treatment for 3 consecutive seasons. The primary outcome was the AAdSS, a symptom score adjusted for rescue medication use, after 3 consecutive treatment seasons. Secondary outcomes were symptoms and rescue medication score, quality-of-life, and safety assessments. Results: The mean AAdSS was reduced by 36.0% and 34.5% at season 3 in the 2- and 4-month pre- and coseasonal active treatment groups, respectively, compared with that in the placebo group (P < .0001 for both). Reductions were observed in total symptom scores and ISSs and the medication score, with a marked improvement in quality of life for both active groups compared with the placebo group at season 3. Most treatment-emergent adverse events were local reactions expected with SLIT, decreasing in number and intensity in each treatment season. Conclusions: Sustained efficacy of 2- and 4-month pre- and coseasonal treatment with the 300 IR tablet over 3 pollen seasons was demonstrated, with reduction in symptoms and rescue medication use. The treatment was well tolerated. Adverse events decreased in number and intensity over the 3 seasons. (J Allergy Clin Immunol 2011;128:559-66.)
引用
收藏
页码:559 / 566
页数:8
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