Short course of grass allergen peptides immunotherapy over 3 weeks reduces seasonal symptoms in allergic rhinoconjunctivitis with/without asthma: A randomized, multicenter, double-blind, placebo-controlled trial
Jazyk angličtina Země Dánsko Médium print-electronic
Typ dokumentu klinické zkoušky, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
Grantová podpora
G1000758
Medical Research Council - United Kingdom
PubMed
29512827
PubMed Central
PMC6175232
DOI
10.1111/all.13433
Knihovny.cz E-zdroje
- Klíčová slova
- Lolium perenne *, clinical trial *, grass pollen *, peptide immunotherapy *, subcutaneous immunotherapy *,
- MeSH
- alergeny aplikace a dávkování imunologie MeSH
- bronchiální astma komplikace imunologie terapie MeSH
- desenzibilizace imunologická * škodlivé účinky metody MeSH
- kvalita života MeSH
- lidé MeSH
- lipnicovité škodlivé účinky MeSH
- peptidy aplikace a dávkování imunologie MeSH
- pyl imunologie MeSH
- roční období MeSH
- rozvrh dávkování léků MeSH
- sezónní alergická rýma komplikace imunologie terapie MeSH
- studie případů a kontrol MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- alergeny MeSH
- peptidy MeSH
BACKGROUND: Immunotherapy with peptide hydrolysates from Lolium perenne (LPP) is an alternative treatment for seasonal allergic rhinitis with or without asthma. The aim of this study was to assess the clinical efficacy and safety of a cumulative dose of 170 μg LPP administered subcutaneously over 3 weeks. METHODS: In a randomized, double-blind, placebo-controlled trial, 554 adults with grass pollen rhinoconjunctivitis were randomized (1:2 ratio) to receive 8 subcutaneous injections of placebo or 170 μg LPP administered in increasing doses in 4 visits over 3 weeks. The primary outcome was the combined symptom and medication score (CSMS) measured over the peak pollen season. Reactivity to conjunctival provocation test (CPT) and quality of life (QOL) was assessed as secondary endpoints. RESULTS: The mean reduction in CSMS in the LPP vs placebo group was -15.5% (P = .041) during the peak period and -17.9% (P = .029) over the entire pollen season. LPP-treated group had a reduced reactivity to CPT (P < .001) and, during the pollen season, a lower rhinoconjunctivitis QOL global score (P = .005) compared with placebo group. Mostly mild and WAO grade 1 early systemic reaction (ESR) were observed ≤30 minutes in 10.5% of LPP-treated patients, whereas 3 patients with a medical history of asthma (<1%) experienced a serious ESR that resolved with rescue medication. CONCLUSION: Lolium perenne pollen peptides administered over 3 weeks before the grass pollen season significantly reduced seasonal symptoms and was generally safe and well-tolerated.
Center for Rhinology and Allergology Wiesbaden Germany
Freelance Biostatistics Consultant Waterloo Belgium
Institute of Medical Statistics Informatics and Epidemiology Cologne Germany
Upper Airways Research Laboratory Ghent University Hospital Ghent Belgium
Zobrazit více v PubMed
Meltzer EO, Blaiss MS, Derebery MJ, et al. Burden of allergic rhinitis: results from the Pediatric Allergies in America survey. J Allergy Clin Immunol. 2009;124(3 suppl):S43‐S70. PubMed
Salo PM, Calatroni A, Gergen PJ, et al. Allergy‐related outcomes in relation to serum IgE: results from the National Health and Nutrition Examination Survey 2005‐2006. J Allergy Clin Immunol. 2011;127:1226‐1235. PubMed PMC
Seidman MD, Gurgel RK, Lin SY, et al. Clinical practice guideline: allergic rhinitis. Otolaryngol Head Neck Surg. 2015;152:S1‐S43. PubMed
Didier A, Malling HJ, Worm M, Horak F, Sussman GL. Prolonged efficacy of the 300IR 5‐grass pollen tablet up to 2 years after treatment cessation, as measured by a recommended daily combined score. Clin Transl Allergy. 2015;5:12. PubMed PMC
Jutel M, Agache I, Bonini S, et al. International consensus on allergy immunotherapy. J Allergy Clin Immunol. 2015;136:556‐568. PubMed
Pfaar O, Bachert C, Bufe A, Buhl R, Ebner C, et al. Guideline on allergen‐specific immunotherapy in IgE‐mediated allergic diseases: S2k Guideline of the German Society for Allergology and Clinical Immunology (DGAKI), the Society for Pediatric Allergy and Environmental Medicine (GPA), the Medical Association of German Allergologists (AeDA), the Austrian Society for Allergy and Immunology (OGAI), the Swiss Society for Allergy and Immunology (SGAI), the German Society of Dermatology (DDG), the German Society of Oto‐ Rhino‐Laryngology, Head and Neck Surgery (DGHNO‐KHC), the German Society of Pediatrics and Adolescent Medicine (DGKJ), the Society for Pediatric Pneumology (GPP), the German Respiratory Society (DGP), the German Association of ENT Surgeons (BV‐HNO), the Professional Federation of Paediatricians and Youth Doctors (BVKJ), the Federal Association of Pulmonologists (BDP) and the German Dermatologists Association (BVDD). Allergo J Int. 2014;23:282‐319. PubMed PMC
Musa F, Al‐Ahmad M, Arifhodzic N, Al‐Herz W. Compliance with allergen immunotherapy and factors affecting compliance among patients with respiratory allergies. Hum Vaccin Immunother. 2017;13:514‐517. PubMed PMC
Reisacher WR, Visaya JM. Patient adherence to allergy immunotherapy. Curr Opin Otolaryngol Head Neck Surg. 2013;21:256‐262. PubMed
Kiel MA, Röder E, van Wijk RG, Al MJ, Hop WCJ, Rutten‐van Mölken MP. Real‐life compliance and persistence among users of subcutaneous and sublingual allergen immunotherapy. J Allergy Clin Immunol. 2013;132:353‐360. PubMed
Moldaver D, Larche M. Immunotherapy with peptides. Allergy. 2011;66:784‐791. PubMed
Shamji MH, Ceuppens J, Bachert C, et al. Lolium perenne peptides for the treatment of grass pollen allergy: a randomized double blind placebo‐controlled clinical trial. J Allergy Clin Immunol. 2018;141:448‐451. PubMed
Mösges R, Kasche EM, Raskopf E, et al. A randomized, double‐blind, placebo‐controlled, dose‐finding trial with Lolium perenne peptide immunotherapy. Lolium perenne peptides: significant efficacy in 3 weeks. Allergy. 2018;73:896‐904. PubMed PMC
Pfaar O, Demoly P, Gerth van Wijk R, et al. Recommendations for the standardization of clinical outcomes used in allergen immunotherapy trials for allergic rhinoconjunctivitis: an EAACI Position Paper. Allergy. 2014;69:854‐867. PubMed
Bousquet J, Van Cauwenberge P, Khaltaev N. Allergic rhinitis and its impact on asthma. J Allergy Clin Immunol. 2001;108:S147‐S334. PubMed
Global Initiative for Asthma . Global strategy for asthma management and prevention. 2014. http://bcrt.ca/wp-content/uploads/2014/05/GINA_Report_2014.pdf. Accessed 10th of June 2017.
Cox L, Larenas‐Linnemann D, Lockey RF, Passalacqua G. Speaking the same language: the world allergy organization subcutaneous immunotherapy systemic reaction grading system. J Allergy Clin Immunol. 2010;125:569‐574. PubMed
Riechelmann H, Epple B, Gropper G. Comparison of conjunctival and nasal provocation test in allergic rhinitis to house dust mite. Int Arch Allergy Immunol. 2003;130:51‐59. PubMed
Dogan S, Astvatsatourov A, Deserno TM, et al. Objectifying the conjunctival provocation test: photography‐based rating and digital analysis. Int Arch Allergy Immunol. 2014;163:59‐68. PubMed
Juniper EF, Thompson AK, Ferrie PJ, Roberts JN. Validation of the standardized version of the Rhinoconjunctivitis Quality of life Questionnaire. J Allergy Clin Immunol. 1999;104:364‐369. PubMed
Juniper EF, Rohrbaugh T, Meltzer EO. A questionnaire to measure quality of life in adults with nocturnal allergic rhinoconjunctivitis. J Allergy Clin Immunol. 2003;111:484‐490. PubMed
European Medicines Agency Committee for Medicinal Products for Human Use . Guideline on Missing Data in Confirmatory Clinical Trials. EMA/CPMP/EWP/1776/99 Rev. 1. 2010. http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2010/09/WC500096793.pdf. Accessed 10th of June 2017.
Pfaar O, Bastl K, Berger U, Buters J, Calderon MA, et al. Defining pollen exposure times for clinical trials of allergen immunotherapy for pollen‐induced rhinoconjunctivitis — an EAACI position paper. Allergy. 2017;72:713‐722. PubMed
Durham SR, Nelson HS, Nolte H, Bernstein DI, Creticos PS, et al. Magnitude of efficacy measurements in grass allergy immunotherapy trials is highly dependent on pollen exposure. Allergy. 2014;69:617‐623. PubMed PMC
Corrigan CJ, Kettner J, Doemer C, Cromwell O, Narkus A. Efficacy and safety of preseasonal‐specific immunotherapy with an aluminium‐adsorbed six‐grass pollen allergoid. Allergy. 2005;60:801‐807. PubMed
DuBuske LM, Frew AJ, Horak F, et al. Ultrashort‐specific immunotherapy successfully treats seasonal allergic rhinoconjunctivitis to grass pollen. Allergy Asthma Proc. 2011;32:239‐247. PubMed
Pfaar O, Urry Z, Robinson DS, et al. A randomized placebo‐controlled trial of rush preseasonal depigmented polymerized grass pollen immunotherapy. Allergy. 2012;67:272‐279. PubMed
Alvarez‐Cuesta E, Bousquet J, Canonica GM, Durham SR, Maling HJ, Valovirta E, EAACI Immunotherapy Task force . Standards for practical allergen‐specific immunotherapy. Allergy. 2006;61:1‐20. PubMed
Iglesias‐Cadarso A, Hernandez‐Weigand P. Risk factors for systemic reactions to allergen immunotherapy. Curr Opin Allergy Clin Immunol. 2011;11:579‐585. PubMed
Dhami S, Nurmatov U, Arasi S, Khan T, Asaria M, et al. Allergen immunotherapy for allergic rhinoconjunctivitis: a systematic review and meta‐analysis. Allergy. 2017;72:1597‐1631. PubMed
Frew AJ, Powell RJ, Corrigan CJ, Durham SR, UK Immunotherapy Study Group . Efficacy and safety of specific immunotherapy with SQ allergen extract in treatment‐resistant seasonal allergic rhinoconjunctivitis. J Allergy Clin Immunol. 2006;117:319‐325. PubMed