Invasive Aspergillosis Clinical Trial
Official title:
An Observational Assessment of the Correlation Between Circulating Galactomannan and Beta-D-glucan and Clinical Outcome in the Setting of Invasive Aspergillosis in Patients With an Underlying Hematological Disorder
The investigators hypothesize that early galactomannan and beta-D-glucan features, namely the height of the initial value at the time of diagnosis and the subsequent rate of marker decay within the first week(s) following therapy (day 7, day 14) are important factors in predicting clinical outcome.
A major challenge in the development of antifungal therapies for invasive fungal infections
is the difficulty in assessing early treatment response and clinical prognosis. Mycological
endpoints are often unreliable, reflected by the low sensitivity of fungal cultures to
diagnose infection (20% for aspergillosis). Radiographic endpoints can be misleading,
particularly when assessed early following treatment initiation. Clinical endpoints can be
ambiguous indicators of treatment response, and generally include categorization of patient
outcome as better, stable or worse. Furthermore, clinical assessments are likely confounded
by the underlying diseases predisposing to fungal infection. Thus, a biomarker interposed
between the initiation of antifungal therapy and patient outcome would bring much needed
precision in the evaluation of novel antifungal drugs and thus serve as a valuable tool to
guide decision-taking regarding ineffective treatments and dose selection in product
development. The current absence of such biomarkers represents a critical capability gap. To
date, only few studies have examined the prognostic value of fungal biomarkers in invasive
aspergillosis on clinical outcome and have been limited by sample seize. To address this
issue, the current study will examine the correlation between the fungal biomarkers
galactomannan and beta-D-glucan with clinical outcome in invasive aspergillosis. The study
will also incorporate C-reactive protein (CRP) levels, as they seem to be a useful surrogate
marker of IL-6 production.
The investigator contains a sample database of 100+ patients with either probable or proven
invasive aspergillosis for which daily marker levels and CRP (during the first two weeks of
antifungal therapy) were measured and clinical assessment data at (2, 4 and ) 6 weeks
post-treatment.
The study will evaluate whether serial serum measurements of galactomannan/beta-D-glucan
during the first week(s) of antifungal therapy can distinguish between successful clinical
outcome and failed clinical outcome at 6 weeks in patients with proven and probable invasive
aspergillosis.
The study aims also at exploring various cut points for galactomannan/beta-D-glucan
measurements at two weeks after initiation of antifungal therapy and at exploring the
sensitivity and specificity for predicting clinical outcome at 6 and 12 weeks in patients
with proven and probable invasive aspergillosis.
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Observational Model: Cohort, Time Perspective: Retrospective
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