Chai, Louis Y. A.;
Kullberg, Bart-Jan;
Johnson, Elizabeth M.;
Teerenstra, Steven;
Khin, Lay Wai;
Vonk, Alieke G.;
Maertens, Johan;
Lortholary, Olivier;
Donnelly, Peter J.;
Schlamm, Haran T.;
Troke, Peter F.;
Netea, Mihai G.;
Herbrecht, Raoul
Early Serum Galactomannan Trend as a Predictor of Outcome of Invasive Aspergillosis
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Media type:
E-Article
Title:
Early Serum Galactomannan Trend as a Predictor of Outcome of Invasive Aspergillosis
Contributor:
Chai, Louis Y. A.;
Kullberg, Bart-Jan;
Johnson, Elizabeth M.;
Teerenstra, Steven;
Khin, Lay Wai;
Vonk, Alieke G.;
Maertens, Johan;
Lortholary, Olivier;
Donnelly, Peter J.;
Schlamm, Haran T.;
Troke, Peter F.;
Netea, Mihai G.;
Herbrecht, Raoul
Published:
American Society for Microbiology, 2012
Published in:
Journal of Clinical Microbiology, 50 (2012) 7, Seite 2330-2336
Language:
English
DOI:
10.1128/jcm.06513-11
ISSN:
0095-1137;
1098-660X
Origination:
Footnote:
Description:
ABSTRACT 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 ≥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 >35% between baseline and week 1 predicted a probability of a satisfactory clinical response. For IA patients with pretreatment GMIs of <0.5 ( n = 131; 64.9%), GMI ought to remain low during treatment, and a rising absolute GMI to >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.