Bronchitis Clinical Trial
Official title:
Mepolizumab in COPD With Eosinophilic Bronchitis: A Randomized Clinical Trial
Some patients with chronic obstructive pulmonary diseases (COPD) have large number of
specific white blood cells called eosinophils in their airways. These cells are also
responsible for causing episodes of worsened respiratory symptoms (exacerbations) and often
cause irreversible damage to the airways . This subset of COPD patients often require oral
steroids to bring down the number of eosinophils in their airways. Steroids have harmful
effects on several of our body systems like bones, blood pressure, blood glucose control and
can cause recurrent infections. Mepolizumab is a drug that specifically targets eosinophils
reducing the number in the airway. This drug has been shown to be effective in decreasing
exacerbation rates and time to exacerbation in asthma patients with eosinophils in their
airways. Targeting eosinophils in COPD patients has been shown to reduce severe
exacerbations. Hence it is likely that COPD patients with eosinophils in their airways will
benefit similarly and have reduced rates and time to exacerbation.
Study Hypothesis:Does mepolizumab decrease sputum eosinophils in patients with fixed airflow
obstruction (COPD) and eosinophilic bronchitis?
The current standard of care of patients with moderate to severe COPD is a combination of
inhaled corticosteroids, long-acting beta agonist and a long-acting muscarinic agonist (3-5).
This treatment recommendation does not consider the heterogeneity of bronchitis in patients
with COPD. A third of patients with COPD without asthma may have an eosinophilic bronchitis
that is likely to respond to inhaled corticosteroids or prednisone. Approximately 1 in 5
exacerbations are also likely to be associated with an eosinophilic exacerbation (6). This is
unlikely to be controlled or prevented by the current recommendations that do not examine
bronchitis at the time of exacerbations. None of the major clinical trials that have
evaluated treatments that form the basis of current guidelines have examined bronchitis at
the time of exacerbations.
Quantitative cell counts in sputum provide a reliable method to assess bronchitis. Sputum can
be safely induced with hypertonic saline even in patients with moderate and severe COPD.
Similarly to asthma (7), the presence of eosinophils in sputum is a predictor of short-term
response in forced expiratory volume at one second (FEV1) and quality of life to inhaled (8)
and oral corticosteroids (9). A single study has demonstrated that normalizing eosinophils in
sputum in patients with COPD reduces severe exacerbations and hospitalizations by
approximately 60% (10). The relative risk reduction in this study is greater than that
demonstrated by any study conducted so far in COPD. Long-term studies have not been
conducted.
Our recent experience with mepolizumab demonstrated that specifically targeting eosinophils
in patient with severe asthma had a prednisone-sparing effect (11) and decrease exacerbations
(11,12). In this study it also improved their lung function including in those patients with
associated COPD. This is not surprising given that persistent airway eosinophilia can
contribute to airway remodeling (13). Indeed, the improvement in FEV1 was associated with a
decrease in sputum hyaluron (14) over the six month treatment period. Changes in lung
function and symptoms have not been consistently observed in previous mepolizumab trials
(12,15). This is clearly related to how precise the patients where phenotyped in terms of
sputum eosinophilia. In studies that recruited patients who had persistent sputum
eosinophilia, decrease in exacerbations were associated with improvements in FEV1 (16).
It is thus likely that a specific treatment such as anti-IL5 directed against eosinophils
would be superior to the current standard treatment in decreasing exacerbations in patients
with COPD who continue to have eosinophils in their airway and whose airway disease has an
eosinophil-driven component as evidenced by persistent airway eosinophilia.
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