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A case of refractory, severe, steroid-dependent asthma Please help! Bruce S. Bochner, M.D. • 24 y/o AA female referred in 2/99 from southern Maryland for evaluation and management of uncontrolled asthma • At the time, 20 weeks pregnant (G5, P4) • Last two pregnancies were complicated by uncontrolled asthma and oral steroid use throughout the pregnancy • H/O asthma since age 12, frequent episodes of wheezing & cough without any obvious triggers or seasonal pattern • Review of accompanying records revealed that her FEV1 can range from 30% to 80% predicted on any given visit • Early on, exacerbations 1x/yr, necessitating ER visits • Initially treated with Cromolyn, Vanceril and Albuterol • Since 1992, worsening asthma, increased ER visits and for 1998 at least 6 hospitalizations • In 1992, found to have multiple positive skin tests, tried on ImTx w/o improvement; in fact, exacerbations of wheezing with most shots • Frequent courses of antibiotics for bronchitis or sinusitis • At the time of her 2/99 visit: – – – – Daily nocturnal symptoms Wheezing with minimal activity Normal CXR managed with Prednisone 30 mg qAM, Flovent 110 2 puffs BID, Serevent 2 puffs BID, Alupent 2 puffs q3h and nebs PRN, Atrovent 4 puffs BID, Accolate 20 mg BID, and Cromolyn q3h • Drug allergy Hx: acute rashes from Penicillin, Codeine, Ceclor; Erythromycin caused GI upset • Environ. Hx: Born and raised in MD, lives in a separate home, no pets • Family Hx: All of her four kids (two different fathers) have asthma; current pregnancy is with a third father • PE: – Vitals: BP 105/66, P 112, RR 18, Wt 168 lbs, peak flow best effort 130 liters/min – GEN: Mild Cushingoid facies, no rashes – HEENT: Nasal exam normal, no lymphadenopathy or thyromegaly – LUNGS: Diffuse expiratory wheezing and prolonged expiratory phase; sounds were in chest but not neck – HEART: Normal S1, S2. – EXTREMITIES: No peripheral edema • SPIROMETRY – FEV1: 1.1 liters (36% predicted), FVC: 1.62 liters (42% predicted), ratio 0.68. Post-bronchodilator FEV1 1.89 liters (79% increase), FVC 2.34 liters (44% increase) • TREATMENT CHANGES – At this visit, patient was switched from Flovent to Pulmicort 4 puffs bid – The rest of her medications were continued – Inhaler technique was observed to be correct – Husband verified medication adherence. • Delivered the baby on continuous nebs. Baby and Mom did fine. 5 weeks postpartum admitted to Hopkins Bayview for 5 days for worsening SOB, wheezing and leg pain • On admission, wheezing; PEF 100 liters/min • V/Q scan and leg dopplers normal • FEV1 28% predicted; flow-volume loops normal • CT scan of sinuses revealed pan-sinusitis • 24-hr pH probe documented significant GERD • Discharged on 24-day steroid taper with markedly improved lung function at discharge; started on antibiotics and Prilosec • Since 2000, multiple ER visits – two prolonged intubations in 2000 and 2001 • 2000: complicated by full respiratory arrest and persistent doll’s eyes • 2001: complicated by bilateral pneumothoraces requiring chest tubes and a DVT; s/p IVC filter • Multiple meds tried in 2000-2001 included Advair, Pulmicort respules, Theophylline, and Methotrexate. None had a significant impact on our ability to taper oral steroids. • In 10/01, sent for an outpatient evaluation by me to National Jewish (made possible through philanthropic help from NJC, AAFA and her local church) with dx of severe, labile steroid-dependent asthma • Diagnosis quickly confirmed when she required admission for worsening SOB and wheezing • • • • • • • • • Skin tests positive to dust mites, grasses, alternaria Alpha-1 antitrypsin: normal CF genotyping: normal No peripheral blood eosinophilia Total IgE: 123 IU/ml Chest CT: no interstitial disease Bone densitometry: normal Sinus CT: mild sinusitis Oral steroid kinetics normal • Seen by Drs. Barry Make and Sally Wenzel • After stabilization with IV steroids and nebs, underwent bronchoscopy • Found to have some collapsibility of her larynx with exhalation which they felt would be helped with CPAP • Sleep study found sleep apnea for which CPAP was also recommended • Bronchoscopy (on IV steroids) revealed prominent basal lamina thickening and a mild inflammatory infiltrate, primarily lymphocytic • After 3 weeks, sent back to Baltimore on the following regimen: – – – – – – – – – – – Serevent 3 puffs q12 QVAR 6 puffs bid Atrovent 4 puffs qid Uniphyl 400 mg qhs Singulair 10 mg qhs Zyflo 600 mg qid Prilosec 40 mg qd Supplemental Calcium Prednisone 40 mg q am, 20 mg q afternoon Nasonex 1 spray bid CPAP • Within 2 months, back to pre-Denver management • 2002 to 2003 – Managed primarily with Prednisone (40-80 mg/day), Prilosec and Albuterol – Extremely Cushingoid; now weighs 240 lbs – Tried Xopenex w/o any additional benefit • September 2003 – Started Xolair one vial q month (completely covered by her insurer) – Still had ER visits but no hospitalizations while on Xolair – Despite this, after seven months, Prenisone, q3h albuteral requirements and FEV1 remained unchanged – She became frustrated, so we discussed other options (Enbrel) and stopped Xolair Pathophysiology of allergic airway inflammation Epithelium Antigen Mast Cell Dendritic Cell TNF IL-1 Activation of Endothelium Chemical Mediators Histamine Leukotrienes, PGD2 Neuropeptides Inflammatory Cytokines TNF, IL-1, GM-CSF "Allergic" Cytokines IL-4, IL-5, IL-9, IL-13 Chemokines Eotaxins, MDC, TARC Enzymes/Toxins Recruitment of Allergic Inflammatory Cells Basophil TH2 Cell Eosinophil End Organ Responses Vascular Leak Smooth Muscle Contraction Mucus Secretion Mast cells as a source of TNFa • Murine mast cells release TNFa following triggering of FceRI – Nature 346:274, 1990 – JEM 174:103, 1991 • Human mast cells release TNFa following triggering of FceRI – PNAS 88:4220, 1991 Model of IgE-dependent acute and chronic allergic inflammatory reactions Acute Chronic Leukocyte recruitment in allergic disease Tissue cells IL-4 IL-5 IL-9 IL-13 ALLERGEN TH2 TNF-a Tissue Blood Vessel Eotaxin Eotaxin-2 RANTES MCP-4 Tissue cells Mast cell TARC MDC TNF-a PGD2 I-309 Tissue cells MDC Eos Baso CCR3 VCAM-1 TH2 Eos Baso Eotaxin-3 Soluble Tumour Necrosis Factor Alpha (TNF-a) Receptor (Enbrel) as an Effective Therapeutic Strategy in Chronic Severe Asthma Babu KS, Arshad SH, Howarth PH, Chauhan AJ, Bell EJ, Puddicombe S, Davies DE, Holgate ST Respiratory Cell & Molecular Biology Southampton University Hospital Southampton, UK JACI 2003 (abstract) Study design • Open label, single center study • Subjects with chronic severe asthma on oral corticosteroids, high dose inhaled corticosteroids, salmeterol, and/or theophylline • 25 mg of Enbrel administered subcutaneous twice a week for 12 weeks Study Design • • • • Subjects aged 18-65 years FEV1 of at least 50% predicted Demonstrated a reversibility of at least 9% Lung function, methacholine response performed before and after treatment • Asthma control symptom questionnaire completed before and after the trial • Diary cards issued to assess peak flows and use of rescue medication Results • • • • • • 15 subjects enrolled in the trial 11 female, 4 male Mean age of the patients: 41 yrs Mean duration of asthma: 24 years Mean dose of oral prednisolone: 12.1mg/day Mean dose of inhaled corticosteroids – 2500 µg/day of beclomethasone or equivalent • Mean dose of nebulised albuterol: 8 mg/day Changes in FEV1 with Enbrel 120 3.00 FEV1 (% predicted) P=0.01 100 2.00 FEV1 % FEV1 (liters) 2.50 1.50 1.00 0.50 0.00 WEEK 1 WEEK 12 80 60 40 20 0 WEEK 1 WEEK 12 Week 1 Week 12 P value FEV1 1.91 2.16 0.01 FVC 2.55 2.88 0.03 Changes in Methacholine Reactivity with Enbrel Methacholine PC20 1000 P=0.033 Log PC20 100 * 10 (1.25) 1 (0.25) 0.1 0.01 WEEK 1 Methacholine AUC WEEK 12 Week 1 Week 12 1.45 (0.98-4.3) 10.6 (3.74-42.61) Changes in Symptom Scores with Enbrel Symptom (Juniper Scale) scoreScores Symptom 35 P<0.001 30 25 20 15 10 5 0 WEEK 1 Symptom score (Juniper Scale) WEEK 12 Week 1 23.8 ± 7.0 Week 12 12.7 ± 8.4 Adverse effects • Skin rashes (4) • Injection site reactions (4) • Respiratory tract infections (7) • Weakly positive ANA (3) Conclusions Treatment with Enbrel in patients with chronic severe asthma: • Improves lung function (FEV1, FEV1/FVC, morning and evening PEF) • Markedly improves asthma control • Markedly improves airway hyperresponsiveness • Markedly reduces the need for rescue medications as all the subjects completely withdrew from their nebulised albuterol by the end of the study • April - early June 2004 – Started Enbrel 25 mg sq twice weekly (completely covered by her insurer) after PPD was negative; husband trained on administration technique – Two weeks later, she was admitted for an asthma exacerbation associated with nausea, fatigue, myalgias and unexplained fevers to 102° despite Enbrel and prednisone; discovered Prilosec had been stopped – Infectious workup unrevealing; IV steroids given – Enbrel dosing held for 2 weeks, fever resolved – Enbrel restarted and 1 week later she was admitted for another asthma exacerbation – Enbrel discontinued • June 21: planned to restart Xolair but got admitted again • Discharged June 22 • Seen June 23 – – – – FEV1 60%; FVC 93% Diffuse wheezing on Prednisone 80 mg Restarted Xolair 300 mg q 4 weeks Restarted Serevent diskus 1 puff BID • What next???? Our ongoing work on TNFa and allergic inflammation • There is a tissue-specific pattern of chemokines/cytokines/adhesion molecules involved in human allergic inflammation • This pattern is TNF-a dependent • The primary source of TNF-a released in human allergic inflammation is the mast cell Etanercept in late phase cutaneous allergic inflammation: study overview • Randomized DBPC Trial • To evaluate effects of etanercept (Enbrel) on cutaneous allergen LPR in 10 perennial allergic rhinitis/dust mite sensitive patients • 15 visits to JHAAC over 8.5 wks • Lead investigators: Lisa Beck, Ed Conner, Bruce Bochner Study Purpose • To evaluate the clinical effects of etanercept on cutaneous allergen challenge late phase responses • To evaluate the effects of etanercept on the allergen dose response • To characterize a variety of biomarkers in the cutaneous late phase responses • To assess limited pharmacokinetic data of etanercept in the serum and nasal washings DBRPC Crossover Study Design 10 pts c DM PAR 7 d Rx Enbrel x 3 vs placebo Overnight Allergen ID titration, blood, nasal washing, skin bx (2 hrs) Baseline eval – skin testing, allergen titration, blood, PPD, sputum, skin bx 25-30 d washout/ recovery Next day 5 PM 7 d Rx Enbrel x 3 vs placebo (crossover) Next day 5 PM Allergen ID titration, blood, nasal washing, skin bx (2 hrs) 9 AM Skin bx (16 hrs) Overnight 9 AM Skin bx (16 hrs)