Early Serum Galactomannan Trend as a Predictor of Outcome of Invasive Aspergillosis

被引:72
作者
Chai, Louis Y. A. [1 ,5 ]
Kullberg, Bart-Jan [1 ]
Johnson, Elizabeth M. [6 ]
Teerenstra, Steven [2 ]
Khin, Lay Wai [7 ]
Vonk, Alieke G. [8 ]
Maertens, Johan [9 ]
Lortholary, Olivier [10 ,11 ,12 ]
Donnelly, Peter J. [3 ,4 ,14 ]
Schlam, Haran T. [13 ]
Troke, Peter F.
Netea, Mihai G. [1 ]
Herbrecht, Raoul [15 ]
机构
[1] Radboud Univ Nijmegen, Dept Med, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Dept Epidemiol Biostat & Hlth Technol Assessment, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Dept Hematol, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[4] Nijmegen Inst Infect Inflammat & Immun N4i, Nijmegen, Netherlands
[5] Natl Univ Hlth Syst, Univ Med Cluster, Div Infect Dis, Singapore, Singapore
[6] Hlth Protect Agcy, Mycol Reference Lab, Bristol, Avon, England
[7] Natl Univ Singapore, Invest Med Unit, Natl Univ Hlth Syst, Singapore 117548, Singapore
[8] Erasmus MC, Univ Med Ctr Rotterdam, Dept Med Microbiol & Infect Dis, Rotterdam, Netherlands
[9] Katholieke Univ Leuven Hosp, Dept Hematol, Louvain, Belgium
[10] Inst Pasteur, Unite Mycol Mol, Ctr Natl Reference Mycol & Antifong, Paris, France
[11] CNRS, URA3012, Paris, France
[12] Univ Paris 05, Hop Necker Enfants Malad, APHP,IHU Imagine, Serv Malad Infect & Trop,Ctr Infectiol Necker Pas, Paris, France
[13] Pfizer Global Res & Dev, New York, NY USA
[14] Old Court, Broadstairs, Kent, England
[15] Hop Univ Strasbourg, Dept Hematol & Oncol, Strasbourg, France
基金
英国医学研究理事会;
关键词
CELL TRANSPLANT RECIPIENTS; SURROGATE END-POINT; ENZYME-IMMUNOASSAY; CIRCULATING GALACTOMANNAN; NEUTROPENIC PATIENTS; ANTIFUNGAL THERAPY; FUNGAL-INFECTION; DIAGNOSIS; ANTIGENEMIA; EPIDEMIOLOGY;
D O I
10.1128/JCM.06513-11
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:2330 / 2336
页数:7
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