Severe Asthma(s): Can THEY be prevented or reversed?

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Severe Asthma(s): Can THEY be prevented or reversed? Sally Wenzel, MD Professor of Medicine UPMC Chair in Translational Airway Biology Disclosures Sally Wenzel, M.D. Grant/Research Support: Boehringer-Ingelheim, Sanofi, GSK, Genentech, AstraZeneca Consultant: Knopp, Aerocrine Umbrella Definition: Severe Asthma Chung et al ERJ 214 requires treatment with high dose inhaled corticosteroids (ICS) ( 1 µg fluticasone propionate or equivalent) plus a second controller (and/or systemic CS) to prevent it from becoming uncontrolled or remains uncontrolled despite this therapy

The Severe Asthmas Severe asthma not a single disease Most clear phenotypes: Childhood onset allergic Always severe Worsening in adulthood Uncommon to slowly progress to severe asthma Adult onset/nasal polyposis Comorbidity associated Autoimmunity/asthmatic granulomatosis Each may require different approaches to prevention/reversal Common Elements of Prevention Have normal lung function at birth and during infancy Pick your parents wisely Genetics of asthma/lung function Make sure Mom doesn t smoke during pregnancy Avoid certain viruses (RSV/RV), especially if you re premature Pick your parents wisely: Genetics of lung function Select mutations in HHIP, PTCH1, FAM13A1, PID1, NOTCH4 associated with lower FEV1 Additive effect of mutations in all 5 associated with lowest FEV1 and highest % severe dz Li, X.E. Bleecker J Allergy Clin Immunol 211

Avoid viral infections (or get preventive immunizations) Fewer asthma attacks, school days missed Wenzel Am J Med 22 Severe bronchiolitis associated with asthma risk, esp in those with asthma FH Sigurs et al AJRCCM 25 Premature infants at risk for RSV and treated with RSV immunoglobulin had less asthma/better lung function 1 yrs later Childhood onset allergic asthma: Genetics and presence of asthma >1, asthma/16, controls Highest p-values for any region were in 17q12-21 in association with CHILDHOOD onset asthma (<16 yrs old) Not seen with adult onset asthma Gene x environment interactions: Dogs protective Moffatt MF et al. A Large Scale Consortium-Based Genomewide Association Study of Asthma N Engl J Med 21;363:1211-1221 Avoid comorbid conditions Holguin F, J Allergy Clin Immunol 211 Adult onset disease associated with both smoking and obesity Obesity in adult onset asthma not associated with disease duration (as it is in childhood onset) Holguin JACI 211 Obesity associated with poorly controlled asthma Both preventable

Can any treatment prevent severe asthma? Early ICS Rx does not prevent asthma progression in children Those who best responded to ICS suffered the most on withdrawal Trials of specific biologics at very early age are needed Guilbert TW et al. N Engl J Med 26;354:1985-1997. Reversal: Type-2 Hi vs Not? Asthma Symptoms Exacerbations FEV1 Type 2 inflammation No/less Type 2 inflammation The promise of biologics? What does it mean to reverse? Prevent progression Bring poorly controlled asthma back to well controlled asthma Permanently improve lung function or remodeling elements Improve asthma control AND reduce medication requirements Likely only modest evidence to suggest can bring poorly controlled asthma back to well controlled

Anti-IL-4Rα in Eos/T2Hi Asthma Multinational, randomized, placebo-controlled study in patients with uncontrolled asthma despite background therapy with medium- to highdose ICS and LABA Patients stratified by blood eosinophil count Hi Eos defined as >3/ul, Lo Eos all others n = 15 Dupilumab 3 mg q2w with loading dose (6 mg) n = 15 Dupilumab 2 mg q2w with loading dose (4 mg) Screening period (14 21 days) Randomization (1:1:1:1:1) n = 15 Dupilumab 3 mg q4w with loading dose (6 mg) Dupilumab was used as add-on therapy to ICS and LABA n = 15 Dupilumab 2 mg q4w with loading dose (4 mg) n = 15 Placebo 24-week treatment period Wenzel, Castro, Corren et al Lancet e-pub 216 q2w, every 2 weeks; q4w, every 4 weeks. Primary endpoint: Change in FEV1 in patients with 3 eos/µl Placebo (n = 68) Dup 2 mg q2w (n = 65) Dup 3 mg q2w (n = 64) LS mean change in FEV 1, L (± SE).5.4.3.2.1 Eos 3 cells/µl 2 4 8 12 Week Wenzel, Castro, Corren et al Lancet e-pub 216 ~75% reduction in steroid requiring asthma exacerbations (6mos) Adjusted annualized severe exacerbation rate, estimate (95% CI) 1.4 1.2 1..8.6.4.2 95% CI.57, 1.9 Placebo (n = 68) 66% 95% CI.16,.81 2 mg q4w (n = 59) Eos 3 cells/µl 35% 95% CI.36, 1.29 3 mg q4w (n = 66) 71% 95% CI.13,.68 95% CI.8,.52 2 mg q2w (n = 64) 81% 3 mg q2w (n = 64) Wenzel, Castro, Corren et et al al Lancet e-pub 216

Could there be immune modification as well? Dupilumab increases blood eos, esp in those with high #s However, after 4-5 mos on Rx, they are back to baseline and perhaps even lower Associated decrease in T2 biomarkers Could inhibition of IL-4R reduce T2 activity? Alternative Type-2: adult onsetnasal polyp/eosinophilic disease Wu, JACI 214 BAL Eosinophil % Mepolizumab consistently effective in 3 large trials of eosinophilic patients Targeted patients with blood eosinophils >~28/ml Reductions in exacerbations of 4-5% Recent studies show impact on FEV1/ACQ as well Responses improve with increasing eosinophils (and likely nasal polyposis/sinus dz) Recently approved by FDA Similar data with reslizumab, benralizumab (anti-il5receptor antibody) Castro Lancet Resp Med 214 and 215 Ortega HG et al. N Engl J Med 214;371:1198-127.

The more blood eos present the better the response (anti-il5r) 19 Anti-IL-5 as CS sparing agent Investigational Product SC every 4 weeks Primary Efficacy Endpoint assessed at week 24 (Exit Visit) Visit 1 Visit 2 Week 4 8 12 16 2 24 Visit 3 4 5 6 7 8 9 OCS Optimisation Phase Induction Phase OCS Reduction Phase Maintenance Phase -8 to -3 weeks Mepolizumab 1mg SC Placebo SC Bel E, et al, N Engl J Med Sept 214 Improvement in asthma control despite reduction in corticosteroids Mean ACQ-5 Score p=.4

Despite persistent eos, >1/3 of SA could not reduce CS dose % study population % Reduction Strata 4% vs 18% OR= 2.39 (95% CI, 1.25-4.56) P=.8 BUT, 3-4% with no/minimal reduction despite starting eosinophilia Other: no decrease in OCS dose, or lack of control during weeks 2-24 or withdrawal from treatment Very severe disease: Beyond Type-2 alone? BAL Eosinophil % BAL Neutrophil % BAL Neutrophils % Higher IFN-γ/Th1 protein in Severe Asthma Compared to Milder Asthma IFN-γ IL-17A IL-5 IL-13 ng/ml 5 2.5.95 ng/ml 2 1.4.2 NS 12 pg/ml 8 4 NS pg/ml 2 15 1 5 Mild-Mod Severe Mild-Mod Severe Mild-Mod Severe Mild-Mod Severe % CD4 + IFN-γ + cells 4 3 2 1 Mild-Mod Severe % CD4 + IL-17A + cells 8 6 4 2 Mild-Mod Severe Voraphani Mucosal Immunol 213, Raundhal et al J Clin Invest 215

Complex (Autoimmune?) Type- 2 reactive airway disease First reported Asthmatic Granulomatosis 212 1 severe asthma pts (now ~35) who met asthma diagnosis (reversibility or + methacholine) All on systemic corticosteroids (1 mg or above) Often adult onset or adult worsening Modest obstruction with decrease in FVC and DLCO Hi FeNO (and blood eos) despite systemic CSs Associated with autoimmune family history in ~7% All underwent VATS surgical biopsies Wenzel Am J Resp Crit Care Med 212 Small airway inflammation and granulomas: complex immunity When associated with personal or family history of autoimmunity respond well to azathioprine Doberer ATS 215 Type 2-Lo Asthma Much less well defined than Type-2 HI Defined as apparent absence of Type 2 No definite endotypes, but many confounders including obesity, post infectious, smoking, long disease duration likely to play a role omics may provide some clues All associated with poor CS response Macrolides, thermoplasty, weight loss

Type 2-Lo late onset obese asthma reverses to weight loss 23 obese asthmatics evaluated before and 12 mos after bariatric surgery Roughly phenotyped patients by median IgE levels (25 vs 35 IU/ml) Late onset asthma=lower IgE Later onset/low IgE obese asthmatics improved PC2 while no effect seen in low IgE/early onset Suggest weight loss will be more effective in some phenotypes Dixon AE et al J Allergy Clin Immunol 211 Unlike anti-il5, anti-il-4rα effective in those with low eos low Type-2?? Placebo Dup 2 mg q2w Dup 3 mg q2w LS mean % change in FEV 1 (± SE) 4 35 3 25 2 15 1 5 Eos 3 cells/µl 2 4 8 12 16 2 24 Week LS mean % change in FEV 1 (± SE) 4 35 3 25 2 15 1 5 Eos < 3 cells/µl 2 4 8 12 16 2 24 Week Efficacy of to IL-4Rα blockade in absence of Type-2 biomarker suggests better biomarkers required!! Wenzel, Castro, Corren Lancet e pub 216 Reduction in FeNO, even in low eos patients on ICS, supports suppression of ongoing Type-2 inflammation LS mean % change in FeNO (± SE) 4 3 2 1 1 2 3 4 5 6 Eos 3 cells/µl 2 4 8 12 16 2 24 Week Placebo Dup 2 mg q2w Dup 3 mg q2w LS mean % change in FeNO (± SE) 4 3 2 1 1 2 3 4 5 6 Eos < 3 cells/µl 2 4 8 12 16 2 24 Week Suggests residual, corticosteroid responsive Type-2 inflammation in large % of patients

Wechsler JACI 213 Thermoplasty: Disease modifying? Short term data reports improvement in AQLQ, possibly exacerbations Longterm data without control group FEV1 declines in 1 st 2 yrs (no statistics given for decline from Baseline to Year 2) Conclusions Prevention of severe asthma(s) is likely dependent on aspects that are difficult to control although maintaining healthy weight in adult hood and never smoking are likely to be helpful Reversal depends on definition Biologics may get us closer by greatly improving outcomes, but ultimate disease modification not yet observed