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    <title>Herbrecht, R.</title>
    <link>http://repub.eur.nl/res/aut/27491/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
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    <item>
      <title>Early Serum Galactomannan Trend as a Predictor of Outcome of
Invasive Aspergillosis (Article)</title>
      <link>http://repub.eur.nl/res/pub/32909/</link>
      <pubDate>2012-07-01T00:00:00Z</pubDate>
      <description>The monitoring and prediction of treatment responses to invasive aspergillosis
      (IA) are difficult. We determined whether serum galactomannan index (GMI) trends 
      early in the course of disease may be useful in predicting eventual clinical
      outcomes. For the subjects recruited into the multicenter Global Aspergillosis
      Study, serial GMIs were measured at baseline and at weeks 1, 2, and 4 following
      antifungal treatment. Clinical response and survival at 12 weeks were the outcome
      measures. GMI trends were analyzed by using the generalized estimation equation
      approach. GMI cutoffs were evaluated by using receiver-operating curve analyses
      incorporating pre- and posttest probabilities. Of the 202 study patients
      diagnosed with IA, 71 (35.1%) had a baseline GMI of &gt;/=0.5. Week 1 GMI was
      significantly lower for the eventual responders to treatment at week 12 than for 
      the nonresponders (GMIs of 0.62 +/- 0.12 and 1.15 +/- 0.22, respectively; P =
      0.035). A GMI reduction of &gt;35% between baseline and week 1 predicted a
      probability of a satisfactory clinical response. For IA patients with
      pretreatment GMIs of &lt;0.5 (n = 131; 64.9%), GMI ought to remain low during
      treatment, and a rising absolute GMI to &gt;0.5 at week 2 despite antifungal
      treatment heralded a poor clinical outcome. Here, every 0.1-unit increase in the 
      GMI between baseline and week 2 increased the likelihood of an unsatisfactory
      clinical response by 21.6% (P = 0.018). In summary, clinical outcomes may be
      anticipated by charting early GMI trends during the first 2 weeks of antifungal
      therapy. These findings have significant implications for the management of IA.
</description>
    </item> <item>
      <title>Early proinflammatory cytokines and C-reactive protein trends as predictors of outcome in invasive aspergillosis (Article)</title>
      <link>http://repub.eur.nl/res/pub/22099/</link>
      <pubDate>2010-11-01T00:00:00Z</pubDate>
      <description>Background. Monitoring treatment response in invasive aspergillosis is challenging, because an immunocompromised host may not exhibit reliable symptoms and clinical signs. Cytokines play a pivotal role in mediating host immune response to infection; therefore, the profiling of biomarkers may be an appropriate surrogate for disease status. Methods. We studied, in a cohort of 119 patients with invasive aspergillosis who were recruited in a multicenter clinical trial, serum interleukin (IL)-6, IL-8, IL-10, interferon-γ, and C-reactive protein (CRP) trends over the first 4 weeks of therapy and correlated these trends to clinical outcome parameters. Results. Circulating IL-6 and CRP levels were high at initiation of therapy and generally showed a downward trend with antifungal treatment. However, subjects with adverse outcomes exhibited a distinct lack of decline in IL-6 and CRP levels at week 1, compared with responders (P = .02, for both IL-6 and CRP). Nonresponders also had significantly elevated IL-8 levels (P = .001). Conclusions. High initial IL-8 and persistently elevated IL-6, IL-8, and CRP levels after initiation of treatment may be early predictors of adverse outcome in invasive aspergillosis. Cytokine and CRP profiles could be used for early identification of patients with a poor response to antifungal treatment who may benefit from more-aggressive antimicrobial regimens. © 2010 by the Infectious Diseases Society of America. All rights reserved.</description>
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