4.5 Article

ECIL recommendations for the use of biological markers for the diagnosis of invasive fungal diseases in leukemic patients and hematopoietic SCT recipients

Journal

BONE MARROW TRANSPLANTATION
Volume 47, Issue 6, Pages 846-854

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/bmt.2011.178

Keywords

galactomannan; beta-glucan; Cryptococcus Ag; mannan; anti-mannan; Aspergillus PCR; invasive fungal diseases

Funding

  1. Foundation for the Advancement in Medical Microbiology and Infectious Diseases, FAMMID, Lausanne, Switzerland
  2. Associates of Cape Code
  3. BioMerieux-Cepheid
  4. Bio-Rad
  5. Wako
  6. Roche Diagnostics
  7. Astellas Pharma
  8. Bristol-Myers Squibb
  9. Cephalon
  10. Gilead Sciences
  11. Glaxo-Smith Kline Beecham
  12. MSD
  13. Novartis
  14. Pfizer
  15. Schering-Plough
  16. Wyeth
  17. Zeneus-Pharma

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As culture-based methods for the diagnosis of invasive fungal diseases (IFD) in leukemia and hematopoietic SCT patients have limited performance, non-culture methods are increasingly being used. The third European Conference on Infections in Leukemia (ECIL-3) meeting aimed at establishing evidence-based recommendations for the use of biological tests in adult patients, based on the grading system of the Infectious Diseases Society of America. The following biomarkers were investigated as screening tests: galactomannan (GM) for invasive aspergillosis (IA); beta-glucan (BG) for invasive candidiasis (IC) and IA; Cryptococcus Ag for cryptococcosis; mannan (Mn) Ag/anti-mannan (A-Mn) Ab for IC, and PCR for IA. Testing for GM, Cryptococcus Ag and BG are included in the revised EORTC/MSG (European Organization for Research and Treatment of Cancer/Mycoses Study Group) consensus definitions for IFD. Strong evidence supports the use of GM in serum (A II), and Cryptococcus Ag in serum and cerebrospinal fluid (CSF) (A II). Evidence is moderate for BG detection in serum (B II), and the combined Mn/A-Mn testing in serum for hepatosplenic candidiasis (B III) and candidemia (C II). No recommendations were formulated for the use of PCR owing to a lack of standardization and clinical validation. Clinical utility of these markers for the early management of IFD should be further assessed in prospective randomized interventional studies. Bone Marrow Transplantation (2012) 47, 846-854; doi:10.1038/bmt.2011.178; published online 19 September 2011

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