Long-term clinical efficacy in grass pollen-induced rhinoconjunctivitis after treatment with SQ-standardized grass allergy immunotherapy tablet

被引:272
作者
Durham, Stephen R. [1 ,2 ]
Emminger, Waltraud [3 ]
Kapp, Alexander [4 ]
Colombo, Giselda [5 ]
de Monchy, Jan G. R. [6 ]
Rak, Sabina [7 ]
Scadding, Glenis K. [8 ]
Andersen, Jens S. [9 ]
Riis, Bente [9 ]
Dahl, Ronald [10 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sect Allergy & Clin Immunol, Natl Heart & Lung Inst, London SW3 6LY, England
[2] Royal Brompton Hosp, London SW3 6LY, England
[3] Allergie Ambulatorium Rennweg, Vienna, Austria
[4] Hannover Med Sch, Dept Dermatol & Allergol, Hannover, Germany
[5] Sci Univ Inst San Raffaele Monte Tabor, Sect Allergy, Milan, Italy
[6] Univ Groningen, Univ Med Ctr Groningen, Sect Allergol Internal Med, Groningen, Netherlands
[7] Sahlgrens Univ Hosp, Sect Allergy, Gothenburg, Sweden
[8] Royal Natl Throat Nose & Ear Hosp, London WC1X 8DA, England
[9] ALK Abello AS, Res & Dev, Horsholm, Denmark
[10] Aarhus Univ Hosp, Dept Resp Dis, Aarhus, Denmark
基金
英国医学研究理事会;
关键词
Allergy immunotherapy tablet; disease modification; grass pollen; immunotherapy; sublingual; sustained efficacy; rhinoconjunctivitis; placebo controlled; Phleum pratense; 6-YEAR FOLLOW-UP; HOUSE-DUST MITE; SUBLINGUAL IMMUNOTHERAPY; IMMUNOLOGICAL CHANGES; CONTROLLED-TRIAL; RHINITIS; SAFETY; CHILDREN; PERFORMANCE; BURDEN;
D O I
10.1016/j.jaci.2009.10.035
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Sustained and disease-modifying effects of sublingual immunotherapy have never before been confirmed in a large-scale randomized, double-blind, placebo-controlled trial. Objective: We sought to investigate sustained efficacy I year after a 3-year period of daily treatment with the SQ-standardized grass allergy immunotherapy tablet Grazax (Phleum pratense 75,000 SQ-T/2,800 BAU; ALK-Abello, Horsholm, Denmark). Methods: A randomized, double-blind, placebo-controlled, phase III trial including adults with a history of moderate-to-severe grass pollen induced rhinoconjunctivitis inadequately controlled by symptomatic medications. The analysis set comprised 257 subjects at the follow-up. Efficacy end points were rhinoconjunctivitis symptom and medication scores, quality of life, and percentages of symptom and medication free days. Immunologic end points included grass pollen-specific serum IgG4 and IgE-blocking factor. Safety was assessed based on adverse events. Results: Significant improvements in efficacy were consistently shown during 3 years' treatment. One year after treatment, the active group showed sustained reductions in mean rhinoconjunctivitis symptom scores (26%, P < .001) and medication scores (29%, P = .022) when compared with placebo. This level was similar to the efficacy observed during the 3-year treatment period. The differences in percentages of symptom- and medication-free days were significant during and I year after treatment. The active group also reported sustained and significant improvements in quality of life. Sustained clinical benefit was accompanied by immunologic changes. No safety issues were identified. Conclusion: Three years of treatment with the SQ-standardized grass allergy immunotherapy tablet resulted in consistent clinical improvement and accompanying immunologic changes that were sustained I year after treatment, which is indicative of disease modification and associated long-term benefits. (J Allergy Clin Immunol 2010;125:131-38.)
引用
收藏
页码:131 / 138
页数:8
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