Efficacy and safety of 5-grass-pollen sublingual immunotherapy tablets in pediatric allergic rhinoconjunctivitis

被引:270
作者
Wahn, Ulrich [1 ]
Tabar, Ana [2 ]
Kuna, Piotr [3 ]
Halken, Susanne [4 ]
Montagut, Armelle [5 ]
de Beaumont, Olivier [6 ]
Le Gall, Martine [6 ]
机构
[1] Charite Campus Virchow Klinikum, Berlin Childrens Hosp, D-13353 Berlin, Germany
[2] Hosp Virgen del Camino, Secc Alergia, Pamplona, Spain
[3] Med Univ Lodz, Div Internal Med Asthma & Allergy, Barlicki Univ Hosp, Lodz, Poland
[4] Odense Univ Denmark, Dept Pediat, Odense, Denmark
[5] Delta Consultants, Meylan, France
[6] Stallergenes SA, Dept Med, Antony, France
关键词
Allergic rhinoconjunctivitis; grass pollen allergy; optimal dose; sublingual tablet; sublingual immunotherapy; children; adolescents; DOUBLE-BLIND; FOLLOW-UP; RHINITIS; ASTHMA; CHILDREN; SYMPTOMS; COLLABORATION; METAANALYSIS;
D O I
10.1016/j.jaci.2008.10.009
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: The efficacy and safety of the 300-index of reactivity (IR) dose of 5-grass-pollen sublingual immunotherapy (SLIT) tablets (Stallergenes, Antony, France) have been demonstrated for the treatment of hay fever in adults. Objective: We sought to assess the efficacy and safety of this tablet in children and adolescents with grass pollen-related allergic rhinitis. Methods: In this multinational, randomized, double-blind, placebo-controlled study, 278 children (5-17 years of age) with grass pollen-related rhinoconjunctivitis (confirmed by means of a positive grass pollen skin prick test response and serum-specific IgE measurement) received once-daily SLIT tablets or placebo. Treatment was initiated 4 months before the estimated pollen season and continued throughout the season. The primary outcome was the rhinoconjunctivitis total symptom score (RTSS), a sum of 6 individual symptom scores: sneezing, runny nose, itchy nose, nasal congestion, watery eyes, and itchy eyes. Secondary end points included rescue medication intake, individual scores, and safety. Results: The intent-to-treat population included 266 children (mean age, 10.9 +/- 3.22 years). The RTSS for the 300-IR group was highly significantly different from that of the placebo group (P = .001). The 300-IR group showed a mean improvement for the RTSS of 28.0% over that seen with placebo and a median improvement of 39.3%. Significant differences between the 300-IR and placebo groups were also observed regarding rescue medication score and proportion of days using rescue medication during the pollen season (P = .0064 and P = .0146, respectively). Adverse events were generally mild or moderate in intensity and expected. No serious side effects were reported. Conclusion: Five-grass-pollen SLIT tablets (300 IR) reduce both symptom scores and rescue medication use in children and adolescents with grass pollen-related rhinoconjunctivitis. (J Allergy Clin Immunol 2009;123:160-6.)
引用
收藏
页码:160 / 166
页数:7
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