Efficacy and safety of the SQ-standardized grass allergy immunotherapy tablet in mono- and polysensitized subjects

被引:81
|
作者
Nelson, H. [1 ]
Blaiss, M. [2 ,3 ]
Nolte, H. [4 ]
Wurtz, S. O. [5 ]
Andersen, J. S. [5 ]
Durham, S. R. [6 ]
机构
[1] Natl Jewish Hlth, Div Allergy & Immunol, Dept Med, Denver, CO USA
[2] Univ Tennessee, Ctr Hlth Sci, Dept Pediat, Memphis, TN 38163 USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Med, Memphis, TN 38163 USA
[4] Merck Res Labs, Kenilworth, NJ USA
[5] ALK Abello, Global Clin Dev, DK-2970 Horsholm, Denmark
[6] Univ London Imperial Coll Sci Technol & Med, NHLI, Sect Allergy & Clin Immunol, London, England
基金
美国国家卫生研究院;
关键词
grass allergy; Phleum pratense; polysensitization; rhinoconjunctivitis; sublingual immunotherapy; SUBLINGUAL IMMUNOTHERAPY; RHINOCONJUNCTIVITIS; RHINITIS; CHILDREN; EXTRACT;
D O I
10.1111/all.12074
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
The efficacy of single-allergen-specific immunotherapy in polysensitized subjects is a matter of debate. We therefore performed a post hoc analysis of pooled data from six randomized, double-blind, placebo-controlled trials (N = 1871) comparing the efficacy and safety of the SQ-standardized grass allergy immunotherapy tablet (AIT), Grazax (Phleum pratense 75 000 SQ-T/2800 BAU, ALK, Denmark), in mono- and polysensitized subjects. A statistically significant reduction in the mean total combined symptom/medication score (TCS) of 27% was demonstrated in actively treated subjects compared with placebo (P < 0.0001). This was not dependent on sensitization status (P = 0.5772), suggesting a similar treatment effect in mono- and polysensitized subjects (i.e. reductions of the TCSs of 28% and 26%, respectively, both P < 0.0001). Finally, a comparable and favourable safety profile of grass AIT was demonstrated in the two subgroups. Thus, no difference in efficacy and safety of single-allergen grass AIT was observed between mono- and polysensitized subjects.
引用
收藏
页码:252 / 255
页数:4
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