COPD is a preventable and treatable disease with patients showing a great disease
heterogeneity with respect to risk of exacerbations, symptomatology and health status.
Dual bronchodilation has been suggested by the recent Global Initiative for Obstructive
Lung Disease guideline as the cornerstone of treatment for COPD, limiting the value
of inhaled corticosteroids (ICS) only for patients exacerbating on dual bronchodilators
or possibly in those with frequent exacerbations.1 Elevated blood eosinophil count
has been suggested as a useful biomarker to guide treatment decisions as its finding
is considered consistent with a good ICS response to treatment,2–4 although this has
been questioned in a recent post hoc analysis of the FLAME study.5 The practicing
physician wants a biomarker to assess the risk of exacerbations and guide treatment
accordingly; are blood eosinophils the answer?
It is important to recognize that we are discussing patients with COPD and without
asthma whose blood eosinophil count is less than 600, as it was in the FLAME study.6
Patients with very high blood eosinophils should be looked at differently (perhaps
as if they have a component of asthma), albeit they were not in the exclusion criterion
in older trials such as WISDOM (>95% of patients had a blood eos <600),7 ISOLDE,8
INSPIRE9 or in a meta-analysis of some of previous studies of budesonide/formoterol.10
In COPD studies wherein asthma was excluded, a blood eosinophil cutoff level of 2%
has been proposed as this shows high sensitivity for predicting sputum eosinophilia.11
Elevation of sputum eosinophils has shown predictability as a marker of ICS response
which has led to the interest in using blood eosinophil count as a surrogate measurement.
However, despite this being biologically plausible, the evidence of the consistency
of blood with sputum/tissue eosinophils is conflicting. Negewo et al showed that blood
eosinophils can help identify the presence or absence of sputum eosinophils,12 while
Turato et al study showed that blood eosinophilia does not reflect tissue eosinophils.13
However, sputum eosinophil count >3% is observed in up to 28% of cases with acute
exacerbations.11 The studies by Negewo et al12 and Bafadhel study10 showed a eosinophil
count of more than 2% in blood served as a biomarker of eosinophil count of >3% in
sputum, and 40% of patients showed a discordance between sputum and blood at the blood
eosinophil cutoff point of 0.3×109/L.11,12 Therefore, there remains significant doubt
as to whether blood eosinophils actually depict tissue and sputum eosinophils.
The Copenhagen Lung Study was recently reviewed, and the results showed an increase
in exacerbations when blood eosinophilia count was above 0.34.14 Conversely, a meta-analysis
by Ho et al which included 14 observational and randomized controlled trials with
parallel groups comparing COPD patients with an elevated blood eosinophil count defined
as having more than 2% of eosinophils, either in the blood or sputum, revealed a similar
risk of both exacerbation at 12 months and in-hospital mortality with or without elevated
blood eosinophil.15
Moreover, a recent study by Casanova et al using data from the CHAIN and BODE cohort
showed that exacerbation rates did not differ in patients with and without eosinophil
counts above 300 cells/μL16 consistent with the ECLISPE study.17 Zysman et al reported
that for all cutoffs, 2% versus <2%, ≥3% versus <3%, and ≥4% versus <4%, there was
no difference between Eos+ and Eos− groups in exacerbation rate, history of asthma,
or three-year survival.18
Eosinophils are not stable throughout the life of a patient with COPD,17,19 and it
has also been reported that blood eosinophil counts vary within the same person at
different times of day and on different days even in healthy subjects.20 This lack
of stability could result in the blood eosinophil not being a reliable biomarker.
A biomarker is only useful if it could be used to assist in disease management. Many
studies have suggested ICS in patients with elevated blood eosinophil count defined
as >2% of total white cells or of a total eosinophils of >300 cells/μL.2–4 However
in most of these studies, the ICS were used in combination with a long-acting beta-agonist
(LABA).3,4 A recent post hoc analysis showed that level of eosinophils may also be
correlated with the response to bronchodilators.21 Similarly, a post hoc analysis
of the FLAME study tested several blood eosinophil cutoff levels and found that there
was no cutoff level to show the ICS-containing salmeterol/fluticasone to be superior
to indacaterol/glycopyrronium (IND/GLY) (ie, LABA/long-acting muscarinic-agonist [LAMA]
with no ICS) in terms of reduction in moderate/severe exacerbation rate or time to
first exacerbation.5 This study did suggest that because IND/GLY is always superior
in patients with low blood eosinophils but of similar efficacy in the groups with
high eosinophil level, blood eosinophils may have a role in identifying patients who
benefit from ICS in addition to LABA/LAMA.5
Elevated blood eosinophil counts are associated with a wide variety of allergic, rheumatologic,
infectious, neoplastic, and rare idiopathic disorders.22 There are many therapies
that can raise eosinophil counts, including medications, nutritional supplements,
and alternative therapies.22,23 COPD patients are multi-morbid and require many non-respiratory
treatments.24 Many commonly prescribed drugs such as amphetamines (used as appetite
suppressants), antibiotics (penicillins, cephalosporins, and sulfonamides), NSAIDs,
ranitidine, allopurinol, antirheumatics, anticonvulsants, aspirin, and tranquilizers
can cause elevated eosinophil counts.22,23 On the other hand, the use of systemic
steroids can decrease eosinophil counts. Therefore, in order for the clinician to
use the blood eosinophil as a biomarker, a complete medication history including over-the-counter
medications, supplements, herbal preparations, and vitamins is necessary.22,23 Future
studies also need to take this into consideration.
While we have been discussing the measurement of blood eosinophils as a percentage
of the total white blood cell counts, most hematology evaluations and treatments are
done based on an absolute count. For instance, in the evaluation of febrile neutropenia,
the absolute neutrophil count is what is used to drive treatment decisions.25 The
absolute eosinophil count refers to the number of circulating eosinophils in the peripheral
blood (in cells/μL). It is determined by multiplying the total white blood cell count
by the percentage of eosinophils. Eosinophil counts are reported differently around
the world, and the clinician may need to calculate the eosinophil count prior to its
use.
Conclusively, while it is exciting to postulate that the blood eosinophils could be
an easily available biomarker to guide the treatment of COPD, in particular to predict
the response to ICS, there are some potential barriers to their use. These include
comorbidities, current medications and treatments, the extra efforts needed to calculate
the eosinophil level, the inconsistency of blood eosinophils with sputum and tissue
eosinophils, the relationship with recent exacerbations, the instability in the level
of blood eosinophils within the same patient at different times of day, and the conditions
and effect of current or recent steroid treatment. Perhaps, we need to recognize that
there is a limitation to this biomarker and tread cautiously in recommending its use.