Invasive Aspergillosis Clinical Trial
Official title:
The Application of an Electronic Nose in the Early Detection of Aspergillosis II
Although the clinical outcome in patients with Invasive Aspergillosis (IA) is largely
dependent on early initiation of effective treatment with antifungal drugs, diagnosing IA is
still a critical problem. Symptoms are non-specific and available diagnostic tools are either
invasive or have low sensitivity and specificity. This often results in a diagnostic delay,
with patients developing more extensive disease. Furthermore, as long as IA is present,
oncological follow-up treatment is not feasible. Inaccuracy in diagnosing IA can cause
serious treatment delay and increased mortality. However, an empirical strategy with
prophylactic anti-mould therapy is not feasible considering both possible side effects and
costs. In order to safely continue the use of a pre-empirical strategy, improved
(non-invasive) diagnostic tools are desirable.
In a pilot study de Heer et al. showed that it is possible to discriminate between patients
with IA and their neutropenic controls by exhaled breath analysis using an electronic nose
(eNose). In this study the investigators aim to test whether an eNose could be useful as a
diagnostic tool in a prospective setting.
The gold standard in exhaled breath analysis is Gas Chromatography - Mass Spectrometry
(GC-MS). This technique enables identification of volatile organic compounds (VOCs) in breath
of patients. It is possible that there are Aspergillus specific VOCs in the breath of
patients with IA.
The composition of the lung microbiome seems to be an important factor in both health and
disease. It is likely that the microbiome of the lung changes in prolonged neutropenia,
therefore possibly creating a niche for molds and yeasts. Comparing the microbiome of
patients with prolonged neutropenia who develop IA with those who do not, can learn us more
about the pathogenesis of this disease. This knowledge could be used to investigate new
treatment options for Invasive Aspergillosis.
Hypothesis The investigators hypothesize that airway microbial (viral, bacterial) presence
and exhaled molecular profiles as obtained from patients with prolonged neutropenia due to
treatment of hematological malignancies, are different between patients who develop IA and
patients who do not.
Aims
1. To compare the exhaled molecular profiles (GC-MS and eNose) between neutropenic patients
who develop IA and neutropenic controls.
2. To investigate whether exhaled molecular profiles can serve as surrogate to predict IA
at an early stage.
3. To compare the alterations in the viral/bacterial microbial profiles during the
neutropenic episode between patients who develop IA and controls.
4. To examine the relationship between microbial and molecular profiles in order to
generate mechanistic hypotheses.
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