REverse LuNg Airway and Vascular RemOdeling in Asthma ReMission (ReNORM)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorWestern University, Canada

About this trial

In this program of research, the investigators aim to answer the question: In patients with asthma aged 18-80, how do the lung airways and vessels respond to biologic therapy and what role does age and asthma duration have in this response? While about 4.6 million Canadians live with asthma, \~5-10% of patients have severe asthma meaning that multiple inhaled and systemic oral corticosteroid treatments have failed to improve symptoms and exacerbations, leading to lost work and school days and substantially diminished ability to participate in normal life. For such people, the vast majority of whom are middle aged and remember asthma as part of their entire lifespan, biologic immunomodulator therapies, which block the function of asthma inflammatory pathways, provide a final step-up therapy option. There is emerging evidence that prescribed in the right patient at the right time, the right biologic can result in clinical remission of asthma. While spontaneous clinical remission of asthma is rare, it has been documented in children in whom lung growth and remodeling is still possible. It remains unknown whether clinical remission in adults is accompanied by the reversal of pathologic remodeling, at the level of the airways and pulmonary vessels. This is critical to elucidate as investigators and physicians move forward with currently proposed criteria for "complete asthma remission". The inconvenient truth about asthma and age is that in older adult lungs, exposed to years of infection, exacerbations, smooth muscle remodeling and pulmonary vascular shunt, the mechanisms by which complete pathologic remission may be achieved are complex and poorly understood.

To address this knowledge gap, the investigators will evaluate 150 patients (Vancouver, Ottawa, Hamilton, London) (in three age tertiles 18-29; 30-59; 60-80) with severe asthma and 50 age- and sex matched healthy volunteers over 2-years using chest CT, MRI and pulmonary function tests. The investigators will use the pulmonary imaging measurements to generate an imaging-index of normal airway structure and function which will be compared with and significantly correlate with MR-guided bronchoscopic sample measurements made before and after 1-/2-years of treatment. The investigators will reveal the pathobiologic relationship between age, asthma duration, clinical remission and imaging normalization with direct comparison to histology-based airway measurements.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Participant understands study procedures and is willing to participate in the study as indicated by the patient's signature.

Provision of written, informed consent prior to any study specific procedures.

Males and females aged 18 to 80 years.

Either diagnosed with severe asthma (GINA Step 5) and newly eligible for biologic therapy (based on ACQ-5, current treatment, exacerbation history, and blood eosinophils in accordance with approved criteria for omalizumab, mepolizumab, benralizumab, dupilumab, or tezepelumab), or a healthy volunteer with no history of chronic lung disease, matched by age and sex. Healthy participants must have a lifetime combustible tobacco and/or cannabis (including vaping) consumption of ≤5 pack-years.

Disqualifiers

Patient has an implanted mechanically, electrically, or magnetically activated device or any metal in their body which cannot be removed, including but not limited to pacemakers, neurostimulators, biostimulators, implanted insulin pumps, aneurysm clips, bioprosthesis, artificial limb, metallic fragment or foreign body, shunt, surgical staples (including clips or metallic sutures and/or ear implants) (at the discretion of the MRI Technologist).

In the investigator's opinion, subject suffers from any physical, psychological or other condition(s) that might prevent performance of the MRI or CT, such as severe claustrophobia.

Participants who are pregnant, breastfeeding or have a positive pregnancy test at initial screening visit.

Participant is unable to perform spirometry or plethysmography maneuvers.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Biologic Therapy

    Biological/Vaccine

    Participants with severe asthma (GINA 5) who are eligible to begin biologic therapy. Participants will undergo serial assessment with pulmonary imaging (CT, MRI), lung function testing, sputum collection, and symptom questionnaires. A subset of participants (\~15%) will be randomized to undergo MRI-guided bronchoscopy with airway sampling at baseline and 2 years.

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Asthma - Biologic TherapyExperimental treatment 1 intervention
Group B: Healthy ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Determine extent of imaging-based remission in patients with severe asthma following 1 and 2 years of biologic therapy

Measured using 129Xe ventilation defect percent (VDP)

Time frame
from baseline to year 1 and year 2
2

Measure the extent and timing of clinical remission in patients with severe asthma as measured by changes in spirometry measurements of FEV1 and FVC

Measured using forced expiratory volume in 1 second and forced vital capacity

Time frame
from baseline to 1 year and 2 years
3

To determine the extent and timing of clinical remission in patients with severe asthma using symptoms scores of ACQ-5 and ACT

Measured using changes in asthma control questionnaire and asthma control test

Time frame
From baseline to 1 year and 2 years
4

Determine the extent and timing of imaging-based remission in patients with severe asthma using CT airway and vessel morphology

Measured using computed tomography (CT) airway and vessel metrics

Time frame
From baseline to 1 year and 2 years

Secondary outcomes

1

Timing and proportion of patients achieving clinical remission after biologic treatment as measured by FEV1 and FVC.

Measured using forced expiratory volume at 1 second and forced vital capacity.

Time frame
From baseline to 1 year and 2 years
2

To determine the timing and proportion of patients achieving clinical remission as measured by ACQ-5 and ACT questionnaires.

Measured by asthma control questionnaire and asthma control test questionnaire scores.

Time frame
From baseline to 1 year and 2 years
3

Determine the timing and proportion of patients with severe asthma achieving clinical remission after biologic treatment using FeNO.

Measured using fractional exhaled nitric oxide (FeNO)

Time frame
From baseline to 1 year and 2 years
4

Determine the timing and proportion of patients with severe asthma achieving clinical remission using DLco.

Measured using diffusing capacity of the lung for carbon monoxide (DLco)

Time frame
From baseline to 1 year and 2 years

Other outcomes

1

Quantify the relationships of imaging and pathologic markers of remodeling and develop a non-invasive imaging-index lung normalization.

Measured using bronchoscopic airway histology (epithelial thickness, smooth muscle mass, vascularity).

Time frame
From baseline (Day 0) to year 2
2

Quantify the relationships of imaging and pathologic markers of remodeling and develop a non-invasive imaging-index lung normalization using MRI/CT correlations with histologic changes

Measured using MRI, CT and histology values

Time frame
From baseline to 2 years.
3

Quantify the relationships of imaging and pathologic markers of remodeling and develop a non-invasive imaging-index lung normalization using MRI/CT fusion data

Measured using MRI and CT measurements

Time frame
From baseline to 2 years.

Sponsors and contacts

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Western University, Canada

Lead sponsor

Canadian Institutes of Health Research (CIHR)

Collaborator

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