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Combination of omalizumab and specific immunotherapy is superior to immunotherapy in patients with seasonal allergic rhinoconjunctivitis and co-morbid seasonal allergic asthma
- Source :
- Clinical & Experimental Allergy. 39:271-279
- Publication Year :
- 2009
- Publisher :
- Wiley, 2009.
-
Abstract
- Summary Background The treatment of allergic asthma by specific immunotherapy (SIT) is hampered by potential side-effects. Objective The aim of this study was to study the effect of omalizumab, a monoclonal anti-IgE antibody, in combination with SIT in patients with seasonal allergic rhinoconjunctivitis (SAR) and co-morbid seasonal allergic asthma (SAA) incompletely controlled by conventional pharmacotherapy. Methods A randomized, double-blind, placebo-controlled, multi-centre trial was performed to assess the efficacy and safety of omalizumab (Xolair®) vs. placebo in combination with depigmented SIT (Depigoid®) during the grass pollen season. Omalizumab or placebo was started 2 weeks before SIT; the whole treatment lasted 18 weeks. Primary endpoint was daily ‘symptom load’, the sum of daily scores for symptom severity and rescue medication use. Results A total of 140 patients (age 11–46 years) were randomized; and a total of 130 finished the study. Combination therapy reduced the symptom load by 39% (P=0.0464, Wilcoxon test) over SIT monotherapy. This difference was mainly due to reduced symptom severity (P=0.0044), while rescue medication use did not change significantly. Combination therapy also improved asthma control (Asthma Control Questionnaire, P=0.0295) and quality of life in the case of asthma (Asthma Quality of Life Questionnaire, P=0.0293) and rhinoconjunctivitis (Rhinoconjunctivitis Quality of Life Questionnaire, P=0.0537). Numbers of patients with ‘excellent or good’ treatment efficacy according to ratings of investigators (75.0% vs. 36.9%) or patients (78.5% vs. 46.1%) were markedly higher in the combination group than under SIT alone. Conclusion Combination of omalizumab with SIT for treatment of patients with SAR and co-morbid SAA was safe and reduced the symptom load in a statistically significant and clinically meaningful manner.
- Subjects :
- Adult
Male
medicine.medical_specialty
Adolescent
Combination therapy
Immunology
Omalizumab
Antibodies, Monoclonal, Humanized
Placebo
law.invention
Young Adult
Pharmacotherapy
Double-Blind Method
Randomized controlled trial
law
Forced Expiratory Volume
Internal medicine
Anti-Allergic Agents
medicine
Clinical endpoint
Humans
Immunology and Allergy
Child
Conjunctivitis, Allergic
Asthma
Plant Extracts
business.industry
Antibodies, Monoclonal
Rhinitis, Allergic, Seasonal
Antigens, Plant
Middle Aged
medicine.disease
Combined Modality Therapy
Antibodies, Anti-Idiotypic
Respiratory Function Tests
Treatment Outcome
Desensitization, Immunologic
Asthma Control Questionnaire
Quality of Life
Physical therapy
Pollen
Female
business
medicine.drug
Subjects
Details
- ISSN :
- 13652222 and 09547894
- Volume :
- 39
- Database :
- OpenAIRE
- Journal :
- Clinical & Experimental Allergy
- Accession number :
- edsair.doi.dedup.....591ad9778012c7a9f1c773b0afd1ad4c
- Full Text :
- https://doi.org/10.1111/j.1365-2222.2008.03121.x