Volume 125, Issue 1 , Pages 131-138.e7, January 2010
Long-term clinical efficacy in grass pollen–induced rhinoconjunctivitis after treatment with SQ-standardized grass allergy immunotherapy tablet
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 1 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-Abelló, Hørsholm, 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 1 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 1 year after treatment, which is indicative of disease modification and associated long-term benefits.
Key words: Allergy immunotherapy tablet, disease modification, grass pollen, immunotherapy, sublingual, sustained efficacy, rhinoconjunctivitis, placebo controlled, Phleum pratense
Abbreviation used: AIT, Allergy immunotherapy tablet
The trial is sponsored by ALK-Abelló, Hørsholm, Denmark. S.R.D. has consultant arrangements with, has received grant support from, and is on the speakers' bureau for ALK-Abelló. A.K. has consultant arrangements with DPC; has received grant support from Novartis, Astellas, UCB, ALK-Abelló, and DPC; and is on the speakers' bureau for Novartis, Astellas, UCB, and ALK. J.G.R.d.M. has received a grant from ALK-Abelló. S.R. has received grant support from the Swedish Asthma and Allergy Association. R.D. has consultant arrangements with Altana, GlaxoSmithKline, Boehringer Ingelheim, Novartis, and Fertin and has received grant support from Altana, GlaxoSmithKline, Boehringer Ingelheim, Novartis, AstraZeneca, ALK-Abelló, Roche, and Pfizer. G.K.S. has been on advisory boards and is on the speakers' bureau for ALK-Abelló and is advisor and speaker for Schering-Plough. J.S.A. and B.R. are employed by ALK-Abelló.
Disclosure of potential conflict of interest: S. R. Durham has received research support from ALK-Abelló and GlaxoSmithKline. W. Emminger and A. Kapp have received research support from ALK-Abelló. J. G. R. de Monchy has received research support from Novartis, Organon (Schering-Plough), and ALK-Abelló. S. Rak has received honoraria from Stallergenes, ALK-Abelló, and Allergopharma and has received research support from ALK-Abelló and Allergopharma. G. K. Scadding is on an advisory board for and has given lectures sponsored by ALK-Abelló and has received research support from ALK-Abelló and GlaxoSmithKline. J. S. Andersen and B. Riis are employees of ALK-Abelló. G. Colombo has declared that she has no conflict of interest.
PII: S0091-6749(09)01583-8
doi:10.1016/j.jaci.2009.10.035
© 2010 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 125, Issue 1 , Pages 131-138.e7, January 2010
