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RECOMMENDATIONS FOR APPROPRIATE SLIT TRIALS Giovanni Passalacqua

RECOMMENDATIONS FOR APPROPRIATE SLIT TRIALS Giovanni Passalacqua. Allergy & Respiratory Diseases Dept.Internal Medicine- IRCCS S.Martino – IST - University of Genoa ITALY CHICAGO-WAO-2013. ISHIZAKA. IgE. NOON. UK CSM. 1986. 2012. Randomized trials. EMPIRICAL USE. 1928.

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RECOMMENDATIONS FOR APPROPRIATE SLIT TRIALS Giovanni Passalacqua

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  1. RECOMMENDATIONS FOR APPROPRIATE SLIT TRIALS Giovanni Passalacqua Allergy & RespiratoryDiseases Dept.Internal Medicine- IRCCS S.Martino – IST - University of Genoa ITALY CHICAGO-WAO-2013

  2. ISHIZAKA IgE NOON UK CSM 1986 2012 Randomized trials EMPIRICAL USE 1928 1960 ROMAGNANI WHO Pos Pap DNA- ITS Mechanisms Allergoids Th1/Th2 SLIT ILIT EPIT Recombinants Liposomes Adjuvants Peptides 1986 1990 1998 2012 DURHAM

  3. Where does IT preferentially works? INFLAMMATION IgE REACTION Atopic dermatitis Hymenoptera Allergy Seasonal rhinitis Asthma Food Allergy Perennial rhinitis

  4. Factors to be evaluate in SIT prescription • 1 IgE mediated disease • 2 Clear identification of the responsible allergen • 3 Severity and duration of symptoms • 4 Efficacy of pharmacological treatment • 5 Compliance • 6 Availability of standardized products • demonstration of the efficacy

  5. WHO Pos Pap. Therapeutical vaccines for allergic diseases Allergy 1998 Standards for practical allergen-specific immunotherapy. Allergy 2006 Allergen immunotherapy: A practice parameter second update JACI 2011

  6. A Meta-analysis and Systematic reviews DBPC trials E.B.M. Evidence Based Medicine Randomized Trials Cohort Studies Case series Case Report, Ideas Editorials, Expert Opinion D EBM Hierarchy

  7. CERTAINTIES - EVIDENCE GREY AREAS UNMET NEEDS UNKNOWN

  8. Tabella meta analisi

  9. JACI 2013

  10. JAMA, 2013

  11. WAO POS PAP 2013

  12. JACI 2011

  13. Symptom Score Rhintis

  14. JACI 2010

  15. CERTAINTIES - EVIDENCE DOUBTFUL UNMET NEEDS UNKNOWN

  16. Quesito clinico (es. efficacia trattamento) GRADE: Grading of Recommendation Assessment, Developing and Evaluation ESAME LETTERATURA Valutazione della qualità della prova sperimentale Sicurezza Preferenza Costo RACCOMANDAZIONE DEBOLE RACCOMANDAZIONE FORTE

  17. Allergic Rhinitis and its Impact on Asthma (ARIA) guidelines: 2010 revision Should subcutaneous specific immunotherapy be used for treatment of AR in adults without concomitant ASTHMA? Recommendation We suggest subcutaneous allergen specific immunotherapy in adults with seasonal AR (conditional recommendation | moderate-quality evidence) and persistent AR caused by mites (conditional recommendation | low-quality evidence). Should subcutaneous specific immunotherapy be used for treatment of in children without concomitant ASTHMA? Recommendation In children with , we suggest subcutaneous specific immunotherapy (conditional recommendation | low-quality evidence).

  18. Allergic Rhinitis and its Impact on Asthma (ARIA) guidelines: 2010 revision Should subcutaneous allergen-specific immunotherapy be used in patients with AR and concomitant asthma? Recommendation In patients with AR and asthma , we suggest subcutaneous specific immunotherapy for treatment of asthma (conditional recommendation | moderate-quality evidence). Should sublingual allergen-specific immunotherapy be used in patients with AR and concomitant asthma ? Recommendation In patients with AR and asthma, we suggest sublingual specific immunotherapy for treatment of asthma (conditional recommendation | low-quality evidence).

  19. JACI 2013

  20. Curr Opin Allergy Clin Immunol 2012

  21. Pham Ti, PAI 2007

  22. March 2009

  23. PROBLEMS: The majority of the trials were not designed and sized for asthma as primary outcome Heterogeneity of study designs, duration, dose and evaluation parameters. Few studies had functional parameters evaluated

  24. Implications for clinical trials: If asthma is investigated, the trial should consider asthma as primary outcome Functional parameters (FEV1, VEMS, oscillometry) should be evaluated Patients should be symptomatic, or therapeutic control should be evaluated.

  25. EIFAN

  26. Implications for clinical trials: The optimal study design to compare SLIT and SCIT is the DB DD RPC fashion This is not currently feasible, due to economic limitations.

  27. ANAPHYLAXES DUE TO SLIT AUTHOR Antico Dunsky Eifan Blazowski Rodriguez De Groot De Groot Buyukozurk Buyukozurk Rodriguez Rodriguez SEX M F F F M M F M M M F AGE 36 31 11 16 11 13 27 28 35 27 7 ALLERG Latex Mix Mix Mite Mite Grass Grass Latex Latex Mite Mite EPINEPH ? N N Y N Y Y Y Y Y Y

  28. JACI 2013

  29. Implications for clinical trials: Adverse events should be described, graded and classified in a standardized fashion Adverse events should be notified promptly, to monitoring authorities or manufacuturers

  30. CERTAINTIES - EVIDENCE DOUBTFUL UNMET NEEDS UNKNOWN

  31. UNSOLVED QUESTIONS Optimal maintenance regimen (continuous VS pre-coseasonal) Dose and extract standardization? Better drugs or SIT? Polysensitized? Optimal maintenance SLIT dose for other allergens

  32. METHODOLOGICAL ISSUES • HETEROGENEITY OF TRIALS • DOSES • PATIENTS’ SELECTION • PRIMARY OUTCOME/ANALYSIS • SAMPLE SIZE CALCULATION • ADHERENCE • REPORTING

  33. Patients with symptoms out of the season

  34. Efficacy and safety of 5-grass-pollen sublingual immunotherapy tablets in pediatric allergic rhinoconjunctivitis Wahn 2009 VS PLACEBO Symptoms • 28% (-39%) Medications - 24% (-48%)

  35. Efficacy and safety of sublingual immunotherapy with grass allergen tablets for seasonal allergic rhinoconjunctivitis. Dahl et al, JACI 2006 VERSUS PLACEBO: SYMPTOM REDUCTION - 30% MEDICATION REDUCTION - 38% 634 PATIENTS !!!

  36. Sastre, Clin Exp Allergy 2010

  37. GRASS Phl p 1 Phl p 5 Phl p 6 Phl p 7 (profilin) Phl p 12 (CBP) BIRCH Bet v 1 Bet v 2 (profilin) Bet v 3 (CBP) PARIETARIA Par j 1 Par j 2 Par j 3 (profilin)

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