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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
来源:
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.
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页码:252 / 255
页数:4
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