Semin Respir Crit Care Med 2024; 45(01): 069-087
DOI: 10.1055/s-0043-1777769
Review Article

Acute Invasive Pulmonary Aspergillosis: Clinical Presentation and Treatment

Jannes Heylen*
1   Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium
,
Yuri Vanbiervliet*
1   Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium
3   Department of Haematology, University Hospitals Leuven, Leuven, Belgium
,
Johan Maertens
1   Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium
3   Department of Haematology, University Hospitals Leuven, Leuven, Belgium
,
Bart Rijnders
4   Department of Internal Medicine and Infectious Diseases, Erasmus MC, University Medical Center, Rotterdam, The Netherlands
,
Joost Wauters
1   Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium
› Author Affiliations

Abstract

Among all clinical manifestations of pulmonary aspergillosis, invasive pulmonary aspergillosis (IPA) is the most acute presentation. IPA is caused by Aspergillus hyphae invading the pulmonary tissue, causing either tracheobronchitis and/or bronchopneumonia. The degree of fungal invasion into the respiratory tissue can be seen as a spectrum, going from colonization to deep tissue penetration with angio-invasion, and largely depends on the host's immune status. Patients with prolonged, severe neutropenia and patients with graft-versus-host disease are at particularly high risk. However, IPA also occurs in other groups of immunocompromised and nonimmunocompromised patients, like solid organ transplant recipients or critically ill patients with severe viral disease. While a diagnosis of proven IPA is challenging and often warranted by safety and feasibility, physicians must rely on a combination of clinical, radiological, and mycological features to assess the likelihood for the presence of IPA. Triazoles are the first-choice regimen, and the choice of the drug should be made on an individual basis. Adjunctive therapy such as immunomodulatory treatment should also be taken into account. Despite an improving and evolving diagnostic and therapeutic armamentarium, the burden and mortality of IPA still remains high. This review aims to give a comprehensive and didactic overview of the current knowledge and best practices regarding the epidemiology, clinical presentation, diagnosis, and treatment of acute IPA.

* Jannes Heylen and Yuri Vanbiervliet have contributed equally to the manuscript.




Publication History

Article published online:
11 January 2024

© 2024. Thieme. All rights reserved.

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  • References

  • 1 van de Veerdonk FL, Gresnigt MS, Romani L, Netea MG, Latgé JP. Aspergillus fumigatus morphology and dynamic host interactions. Nat Rev Microbiol 2017; 15 (11) 661-674
  • 2 Donnelly JP, Chen SC, Kauffman CA. et al. Revision and update of the consensus definitions of invasive fungal disease from the European Organization for Research and Treatment of Cancer and the Mycoses Study Group Education and Research Consortium. Clin Infect Dis 2020; 71 (06) 1367-1376
  • 3 Cornillet A, Camus C, Nimubona S. et al. Comparison of epidemiological, clinical, and biological features of invasive aspergillosis in neutropenic and nonneutropenic patients: a 6-year survey. Clin Infect Dis 2006; 43 (05) 577-584
  • 4 Vandewoude KH, Blot SI, Depuydt P. et al. Clinical relevance of Aspergillus isolation from respiratory tract samples in critically ill patients. Crit Care 2006; 10 (01) R31
  • 5 Meersseman W, Vandecasteele SJ, Wilmer A, Verbeken E, Peetermans WE, Van Wijngaerden E. Invasive aspergillosis in critically ill patients without malignancy. Am J Respir Crit Care Med 2004; 170 (06) 621-625
  • 6 Baddley JW, Stephens JM, Ji X, Gao X, Schlamm HT, Tarallo M. Aspergillosis in intensive care unit (ICU) patients: epidemiology and economic outcomes. BMC Infect Dis 2013; 13 (01) 29
  • 7 Taccone FS, Van den Abeele AM, Bulpa P. et al; AspICU Study Investigators. Epidemiology of invasive aspergillosis in critically ill patients: clinical presentation, underlying conditions, and outcomes. Crit Care 2015; 19 (01) 7
  • 8 Bulpa P, Dive A, Sibille Y. Invasive pulmonary aspergillosis in patients with chronic obstructive pulmonary disease. Eur Respir J 2007; 30 (04) 782-800
  • 9 Lahmer T, Peçanha-Pietrobom PM, Schmid RM, Colombo AL. Invasive fungal infections in acute and chronic liver impairment: a systematic review. Mycoses 2022; 65 (02) 140-151
  • 10 Wauters J, Baar I, Meersseman P. et al. Invasive pulmonary aspergillosis is a frequent complication of critically ill H1N1 patients: a retrospective study. Intensive Care Med 2012; 38 (11) 1761-1768
  • 11 Schauwvlieghe AFAD, Rijnders BJA, Philips N. et al; Dutch-Belgian Mycosis study group. Invasive aspergillosis in patients admitted to the intensive care unit with severe influenza: a retrospective cohort study. Lancet Respir Med 2018; 6 (10) 782-792
  • 12 Gangneux JP, Dannaoui E, Fekkar A. et al. Fungal infections in mechanically ventilated patients with COVID-19 during the first wave: the French multicentre MYCOVID study. Lancet Respir Med 2022; 10 (02) 180-190
  • 13 Prattes J, Wauters J, Giacobbe DR. et al; ECMM-CAPA Study Group. Risk factors and outcome of pulmonary aspergillosis in critically ill coronavirus disease 2019 patients-a multinational observational study by the European Confederation of Medical Mycology. Clin Microbiol Infect 2022; 28 (04) 580-587
  • 14 Janssen NAF, Nyga R, Vanderbeke L. et al. Multinational observational cohort study of COVID-19-associated pulmonary aspergillosis. Emerg Infect Dis 2021; 27 (11) 2892-2898
  • 15 Kluge S, Strauß R, Kochanek M, Weigand MA, Rohde H, Lahmer T. Aspergillosis: emerging risk groups in critically ill patients. Med Mycol 2021; 60 (01) myab064
  • 16 Brown GD, Denning DW, Gow NAR, Levitz SM, Netea MG, White TC. Hidden killers: human fungal infections. Sci Transl Med 2012; 4 (165) 165rv13
  • 17 World Health Organization. WHO fungal priority pathogens list to guide research, development and public health action. 2022 Accessed November 24, 2023 at: https://www.who.int/publications/i/item/9789240060241
  • 18 Bongomin F, Gago S, Oladele RO, Denning DW. Global and multi-national prevalence of fungal diseases-estimate precision. J Fungi (Basel) 2017; 3 (04) 57
  • 19 Ascioglu S, Rex JH, de Pauw B. et al; Invasive Fungal Infections Cooperative Group of the European Organization for Research and Treatment of Cancer, ; Mycoses Study Group of the National Institute of Allergy and Infectious Diseases. Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: an international consensus. Clin Infect Dis 2002; 34 (01) 7-14
  • 20 De Pauw B, Walsh TJ, Donnelly JP. et al; European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group, ; National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group. Revised definitions of invasive fungal disease from the European Organization for Research and Treatment of Cancer/Invasive Fungal Infections Cooperative Group and the National Institute of Allergy and Infectious Diseases Mycoses Study Group (EORTC/MSG) Consensus Group. Clin Infect Dis 2008; 46 (12) 1813-1821
  • 21 Latgé J-P. Aspergillus fumigatus and aspergillosis. Clin Microbiol Rev 1999; 12 (02) 310-350
  • 22 Gerson SL, Talbot GH, Hurwitz S, Strom BL, Lusk EJ, Cassileth PA. Prolonged granulocytopenia: the major risk factor for invasive pulmonary aspergillosis in patients with acute leukemia. Ann Intern Med 1984; 100 (03) 345-351
  • 23 Wald A, Leisenring W, van Burik JA, Bowden RA. Epidemiology of aspergillus infections in a large cohort of patients undergoing bone marrow transplantation. J Infect Dis 1997; 175 (06) 1459-1466
  • 24 Marr KA, Carter RA, Boeckh M, Martin P, Corey L. Invasive aspergillosis in allogeneic stem cell transplant recipients: changes in epidemiology and risk factors. Blood 2002; 100 (13) 4358-4366
  • 25 Jantunen E, Ruutu P, Niskanen L. et al. Incidence and risk factors for invasive fungal infections in allogeneic BMT recipients. Bone Marrow Transplant 1997; 19 (08) 801-808
  • 26 Kontoyiannis DP, Marr KA, Park BJ. et al. Prospective surveillance for invasive fungal infections in hematopoietic stem cell transplant recipients, 2001-2006: overview of the Transplant-Associated Infection Surveillance Network (TRANSNET) Database. Clin Infect Dis 2010; 50 (08) 1091-1100
  • 27 Denning DW, Marinus A, Cohen J. et al; EORTC Invasive Fungal Infections Cooperative Group. An EORTC multicentre prospective survey of invasive aspergillosis in haematological patients: diagnosis and therapeutic outcome. J Infect 1998; 37 (02) 173-180
  • 28 Lin SJ, Schranz J, Teutsch SM. Aspergillosis case-fatality rate: systematic review of the literature. Clin Infect Dis 2001; 32 (03) 358-366
  • 29 Tortorano AM, Dho G, Prigitano A. et al; ECMM-FIMUA Study Group. Invasive fungal infections in the intensive care unit: a multicentre, prospective, observational study in Italy (2006-2008). Mycoses 2012; 55 (01) 73-79
  • 30 Thevissen K, Jacobs C, Holtappels M, Toda M, Verweij P, Wauters J. International survey on influenza-associated pulmonary aspergillosis (IAPA) in intensive care units: responses suggest low awareness and potential underdiagnosis outside Europe. Crit Care 2020; 24 (01) 84
  • 31 Roosen J, Frans E, Wilmer A, Knockaert DC, Bobbaers H. Comparison of premortem clinical diagnoses in critically ill patients and subsequent autopsy findings. Mayo Clin Proc 2000; 75 (06) 562-567
  • 32 Winters B, Custer J, Galvagno Jr SM. et al. Diagnostic errors in the intensive care unit: a systematic review of autopsy studies. BMJ Qual Saf 2012; 21 (11) 894-902
  • 33 Vanderbeke L, Jacobs C, Feys S. et al. A pathology-based case series of influenza- and COVID-19-associated pulmonary aspergillosis: the proof is in the tissue. Am J Respir Crit Care Med 2023; 208 (03) 301-311
  • 34 Tejerina EE, Abril E, Padilla R. et al. Invasive aspergillosis in critically ill patients: an autopsy study. Mycoses 2019; 62 (08) 673-679
  • 35 Global Initiative for Chronic Obstructive Lung Disease (GOLD). Global strategy for prevention, diagnosis and management of COPD: 2023 Report. Accessed November 24, 2023 at: https://goldcopd.org/2023-gold-report-2/
  • 36 Mir T, Uddin M, Khalil A. et al. Mortality outcomes associated with invasive aspergillosis among acute exacerbation of chronic obstructive pulmonary disease patient population. Respir Med 2022; 191: 106720
  • 37 Guinea J, Torres-Narbona M, Gijón P. et al. Pulmonary aspergillosis in patients with chronic obstructive pulmonary disease: incidence, risk factors, and outcome. Clin Microbiol Infect 2010; 16 (07) 870-877
  • 38 Hammond EE, McDonald CS, Vestbo J, Denning DW. The global impact of Aspergillus infection on COPD. BMC Pulm Med 2020; 20 (01) 241
  • 39 Denning DW. Calling upon all public health mycologists : to accompany the country burden papers from 14 countries. Eur J Clin Microbiol Infect Dis 2017; 36 (06) 923-924
  • 40 Garnacho-Montero J, Olaechea P, Alvarez-Lerma F. et al. Epidemiology, diagnosis and treatment of fungal respiratory infections in the critically ill patient. Rev Esp Quimioter 2013; 26 (02) 173-188
  • 41 Lionakis MS, Kontoyiannis DP. Glucocorticoids and invasive fungal infections. Lancet 2003; 362 (9398) 1828-1838
  • 42 Barouky R, Badet M, Denis MS, Soubirou JL, Philit F, Guerin C. Inhaled corticosteroids in chronic obstructive pulmonary disease and disseminated aspergillosis. Eur J Intern Med 2003; 14 (06) 380-382
  • 43 Leav BA, Fanburg B, Hadley S. Invasive pulmonary aspergillosis associated with high-dose inhaled fluticasone. N Engl J Med 2000; 343 (08) 586-586
  • 44 Peter E, Bakri F, Ball DM, Cheney RT, Segal BH. Invasive pulmonary filamentous fungal infection in a patient receiving inhaled corticosteroid therapy. Clin Infect Dis 2002; 35 (05) e54-e56
  • 45 Bulpa P, Bihin B, Dimopoulos G. et al; AspICU study investigators. Which algorithm diagnoses invasive pulmonary aspergillosis best in ICU patients with COPD?. Eur Respir J 2017; 50 (03) 1700532
  • 46 Patel DA, Gao X, Stephens JM, Forshag MS, Tarallo M. US hospital database analysis of invasive aspergillosis in the chronic obstructive pulmonary disease non-traditional host. J Med Econ 2011; 14 (02) 227-237
  • 47 Barberan J, Sanz F, Hernandez JL. et al. Clinical features of invasive pulmonary aspergillosis vs. colonization in COPD patients distributed by gold stage. J Infect 2012; 65 (05) 447-452
  • 48 Delsuc C, Cottereau A, Frealle E. et al. Putative invasive pulmonary aspergillosis in critically ill patients with chronic obstructive pulmonary disease: a matched cohort study. Crit Care 2015; 19 (01) 421
  • 49 Albillos A, Lario M, Álvarez-Mon M. Cirrhosis-associated immune dysfunction: distinctive features and clinical relevance. J Hepatol 2014; 61 (06) 1385-1396
  • 50 Irvine KM, Ratnasekera I, Powell EE, Hume DA. Causes and consequences of innate immune dysfunction in cirrhosis. Front Immunol 2019; 10: 293
  • 51 Thursz M, Gual A, Lackner C. et al; European Association for the Study of the Liver. Electronic address: easloffice@easloffice.eu, ; European Association for the Study of the Liver. EASL clinical practice guidelines: management of alcohol-related liver disease. J Hepatol 2018; 69 (01) 154-181
  • 52 Verma N, Singh S, Taneja S. et al. Invasive fungal infections amongst patients with acute-on-chronic liver failure at high risk for fungal infections. Liver Int 2019; 39 (03) 503-513
  • 53 Lahmer T, Messer M, Schwerdtfeger C. et al. Invasive mycosis in medical intensive care unit patients with severe alcoholic hepatitis. Mycopathologia 2014; 177 (3–4): 193-197
  • 54 Gustot T, Maillart E, Bocci M. et al. Invasive aspergillosis in patients with severe alcoholic hepatitis. J Hepatol 2014; 60 (02) 267-274
  • 55 Levesque E, Ait-Ammar N, Dudau D. et al. Invasive pulmonary aspergillosis in cirrhotic patients: analysis of a 10-year clinical experience. Ann Intensive Care 2019; 9 (01) 31
  • 56 Alshabani K, Haq A, Miyakawa R, Palla M, Soubani AO. Invasive pulmonary aspergillosis in patients with influenza infection: report of two cases and systematic review of the literature. Expert Rev Respir Med 2015; 9 (01) 89-96
  • 57 van de Veerdonk FL, Kolwijck E, Lestrade PPA. et al; Dutch Mycoses Study Group. Influenza-associated aspergillosis in critically ill patients. Am J Respir Crit Care Med 2017; 196 (04) 524-527
  • 58 Vanderbeke L, Janssen NAF, Bergmans DCJJ. et al; Dutch-Belgian Mycosis Study Group. Posaconazole for prevention of invasive pulmonary aspergillosis in critically ill influenza patients (POSA-FLU): a randomised, open-label, proof-of-concept trial. Intensive Care Med 2021; 47 (06) 674-686
  • 59 Shi C, Shan Q, Xia J. et al. Incidence, risk factors and mortality of invasive pulmonary aspergillosis in patients with influenza: a systematic review and meta-analysis. Mycoses 2022; 65 (02) 152-163
  • 60 Wu CJ, Cia CT, Wang HC. et al. Clinical and microbiological characteristics of culture-positive, influenza-associated pulmonary aspergillosis: a single-center study in southern Taiwan, 2016-2019. J Fungi (Basel) 2022; 8 (01) 49
  • 61 Schwartz IS, Friedman DZP, Zapernick L. et al. High rates of influenza-associated invasive pulmonary aspergillosis may not be universal: a retrospective cohort study from Alberta, Canada. Clin Infect Dis 2020; 71 (07) 1760-1763
  • 62 Coste A, Frérou A, Raute A. et al. The extent of aspergillosis in critically ill patients with severe influenza pneumonia: a multicenter cohort study. Crit Care Med 2021; 49 (06) 934-942
  • 63 Martin-Loeches I, , J Schultz M, Vincent JL. et al. Increased incidence of co-infection in critically ill patients with influenza. Intensive Care Med 2017; 43 (01) 48-58
  • 64 Prattes J, Koehler P, Hoenigl M. ECMM-CAPA Study Group. COVID-19 associated pulmonary aspergillosis: regional variation in incidence and diagnostic challenges. Intensive Care Med 2021; 47 (11) 1339-1340
  • 65 Feys S, Almyroudi MP, Braspenning R. et al. A visual and comprehensive review on COVID-19-associated pulmonary aspergillosis (CAPA). J Fungi (Basel) 2021; 7 (12) 1067
  • 66 Agrawal U, Bedston S, McCowan C. et al. Severe COVID-19 outcomes after full vaccination of primary schedule and initial boosters: pooled analysis of national prospective cohort studies of 30 million individuals in England, Northern Ireland, Scotland, and Wales. Lancet 2022; 400 (10360): 1305-1320
  • 67 Fung M, Babik JM. COVID-19 in immunocompromised hosts: what we know so far. Clin Infect Dis 2021; 72 (02) 340-350
  • 68 Sun J, Zheng Q, Madhira V. et al; National COVID Cohort Collaborative (N3C) Consortium. Association between immune dysfunction and COVID-19 breakthrough infection after SARS-CoV-2 vaccination in the US. JAMA Intern Med 2022; 182 (02) 153-162
  • 69 Feys S, Lagrou K, Lauwers HM. et al. High burden of COVID-19-associated pulmonary aspergillosis (CAPA) in severely immunocompromised patients requiring mechanical ventilation. Clin Infect Dis 2023 DOI: 10.1093/cid/ciad546
  • 70 White PL, Dhillon R, Cordey A. et al. A national strategy to diagnose coronavirus disease 2019-associated invasive fungal disease in the intensive care unit. Clin Infect Dis 2021; 73 (07) e1634-e1644
  • 71 Bartoletti M, Pascale R, Cricca M. et al; PREDICO Study Group. Epidemiology of invasive pulmonary aspergillosis among intubated patients with COVID-19: a prospective study. Clin Infect Dis 2021; 73 (11) e3606-e3614
  • 72 Husain S, Mooney ML, Danziger-Isakov L. et al; ISHLT Infectious Diseases Council Working Group on Definitions. A 2010 working formulation for the standardization of definitions of infections in cardiothoracic transplant recipients. J Heart Lung Transplant 2011; 30 (04) 361-374
  • 73 Cahill BC, Hibbs JR, Savik K. et al. Aspergillus airway colonization and invasive disease after lung transplantation. Chest 1997; 112 (05) 1160-1164
  • 74 Singh N, Husain S. AST Infectious Diseases Community of Practice. Aspergillosis in solid organ transplantation. Am J Transplant 2013; 13 (suppl 4): 228-241
  • 75 Felton TW, Roberts SA, Isalska B. et al. Isolation of Aspergillus species from the airway of lung transplant recipients is associated with excess mortality. J Infect 2012; 65 (04) 350-356
  • 76 Nyga R, Maizel J, Nseir S. et al. Invasive tracheobronchial aspergillosis in critically ill patients with severe influenza. a clinical trial. Am J Respir Crit Care Med 2020; 202 (05) 708-716
  • 77 van de Veerdonk FL, Brüggemann RJM, Vos S. et al. COVID-19-associated Aspergillus tracheobronchitis: the interplay between viral tropism, host defence, and fungal invasion. Lancet Respir Med 2021; 9 (07) 795-802
  • 78 Singh N, Husain S. Aspergillus infections after lung transplantation: clinical differences in type of transplant and implications for management. J Heart Lung Transplant 2003; 22 (03) 258-266
  • 79 Koehler P, Bassetti M, Kochanek M, Shimabukuro-Vornhagen A, Cornely OA. Intensive care management of influenza-associated pulmonary aspergillosis. Clin Microbiol Infect 2019; 25 (12) 1501-1509
  • 80 Fernández-Ruiz M, Silva JT, San-Juan R. et al. Aspergillus tracheobronchitis: report of 8 cases and review of the literature. Medicine (Baltimore) 2012; 91 (05) 261-273
  • 81 Denning DW. Invasive aspergillosis. Clin Infect Dis 1998; 26 (04) 781-803 , quiz 804–805
  • 82 Ullmann AJ, Aguado JM, Arikan-Akdagli S. et al. Diagnosis and management of Aspergillus diseases: executive summary of the 2017 ESCMID-ECMM-ERS guideline. Clin Microbiol Infect 2018; 24 (suppl 1): e1-e38
  • 83 Patterson TF, Thompson III GR, Denning DW. et al. Practice guidelines for the diagnosis and management of aspergillosis: 2016 update by the Infectious Diseases Society of America. Clin Infect Dis 2016; 63 (04) e1-e60
  • 84 Park SY, Lim C, Lee SO. et al. Computed tomography findings in invasive pulmonary aspergillosis in non-neutropenic transplant recipients and neutropenic patients, and their prognostic value. J Infect 2011; 63 (06) 447-456
  • 85 Fraser RS. Pulmonary aspergillosis: pathologic and pathogenetic features. Pathol Annu 1993; 28 (Pt 1): 231-277
  • 86 Kibbler CC, Milkins SR, Bhamra A, Spiteri MA, Noone P, Prentice HG. Apparent pulmonary mycetoma following invasive aspergillosis in neutropenic patients. Thorax 1988; 43 (02) 108-112
  • 87 Meziane MA, Hruban RH, Zerhouni EA. et al. High resolution CT of the lung parenchyma with pathologic correlation. Radiographics 1988; 8 (01) 27-54
  • 88 Slevin ML, Knowles GK, Phillips MJ, Stansfeld AG, Lister TA. The air crescent sign of invasive pulmonary aspergillosis in acute leukaemia. Thorax 1982; 37 (07) 554-555
  • 89 Ascah KJ, Hyland RH, Hutcheon MA. et al. Invasive aspergillosis in a “healthy” patient. Can Med Assoc J 1984; 131 (04) 332-335
  • 90 Sassi C, Stanzani M, Lewis RE. et al. The utility of contrast-enhanced hypodense sign for the diagnosis of pulmonary invasive mould disease in patients with haematological malignancies. Br J Radiol 2018; 91 (1083): 20170220
  • 91 Brodoefel H, Vogel M, Hebart H. et al. Long-term CT follow-up in 40 non-HIV immunocompromised patients with invasive pulmonary aspergillosis: kinetics of CT morphology and correlation with clinical findings and outcome. AJR Am J Roentgenol 2006; 187 (02) 404-413
  • 92 Caillot D, Couaillier JF, Bernard A. et al. Increasing volume and changing characteristics of invasive pulmonary aspergillosis on sequential thoracic computed tomography scans in patients with neutropenia. J Clin Oncol 2001; 19 (01) 253-259
  • 93 Alexander BD, Lamoth F, Heussel CP. et al. Guidance on imaging for invasive pulmonary aspergillosis and mucormycosis: from the Imaging Working Group for the Revision and Update of the Consensus Definitions of Fungal Disease from the EORTC/MSGERC. Clin Infect Dis 2021; 72 (suppl 2): S79-S88
  • 94 Douglas A, Thursky K, Spelman T. et al. [18F]FDG-PET-CT compared with CT for persistent or recurrent neutropenic fever in high-risk patients (PIPPIN): a multicentre, open-label, phase 3, randomised, controlled trial. Lancet Haematol 2022; 9 (08) e573-e584
  • 95 Camus V, Edet-Sanson A, Bubenheim M. et al. 18F-FDG-PET/CT imaging in patients with febrile neutropenia and haematological malignancies. Anticancer Res 2015; 35 (05) 2999-3005
  • 96 Prebil SEW, Andrews J, Cribbs SK, Martin GS, Esper A. Safety of research bronchoscopy in critically ill patients. J Crit Care 2014; 29 (06) 961-964
  • 97 Douglas AP, Smibert OC, Bajel A. et al; Australasian Antifungal Guidelines Steering Committee. Consensus guidelines for the diagnosis and management of invasive aspergillosis, 2021. Intern Med J 2021; 51 (suppl 7): 143-176
  • 98 Wormser GP, Stratton C. Manual of Clinical Microbiology, 9th Edition Edited by Patrick R. Murray, Ellen Jo Baron, James H. Jorgensen, Marie Louise Landry, and Michael A. Pfaller Washington, DC: ASM Press, 2007 2488 pp., illustrated. $209.95 (hardcover). Clin Infect Dis 2008; 46 (01) 153
  • 99 Girmenia C, Nucci M, Martino P. Clinical significance of Aspergillus fungaemia in patients with haematological malignancies and invasive aspergillosis. Br J Haematol 2001; 114 (01) 93-98
  • 100 Koehler P, Bassetti M, Chakrabarti A. et al; European Confederation of Medical Mycology, ; International Society for Human Animal Mycology, ; Asia Fungal Working Group, ; INFOCUS LATAM/ISHAM Working Group, ; ISHAM Pan Africa Mycology Working Group, ; European Society for Clinical Microbiology, ; Infectious Diseases Fungal Infection Study Group, ; ESCMID Study Group for Infections in Critically Ill Patients, ; Interregional Association of Clinical Microbiology and Antimicrobial Chemotherapy, ; Medical Mycology Society of Nigeria, ; Medical Mycology Society of China Medicine Education Association, ; Infectious Diseases Working Party of the German Society for Haematology and Medical Oncology, ; Association of Medical Microbiology, ; Infectious Disease Canada. Defining and managing COVID-19-associated pulmonary aspergillosis: the 2020 ECMM/ISHAM consensus criteria for research and clinical guidance. Lancet Infect Dis 2021; 21 (06) e149-e162
  • 101 Roman-Montes CM, Martinez-Gamboa A, Diaz-Lomelí P. et al. Accuracy of galactomannan testing on tracheal aspirates in COVID-19-associated pulmonary aspergillosis. Mycoses 2021; 64 (04) 364-371
  • 102 Verweij PE, Brüggemann RJM, Azoulay E. et al. Taskforce report on the diagnosis and clinical management of COVID-19 associated pulmonary aspergillosis. Intensive Care Med 2021; 47 (08) 819-834
  • 103 Blot S, Rello J, Koulenti D. Diagnosing invasive pulmonary aspergillosis in ICU patients: putting the puzzle together. Curr Opin Crit Care 2019; 25 (05) 430-437
  • 104 Mercier T, Castagnola E, Marr KA, Wheat LJ, Verweij PE, Maertens JA. Defining galactomannan positivity in the updated EORTC/MSGERC consensus definitions of invasive fungal diseases. Clin Infect Dis 2021; 72 (suppl 2): S89-S94
  • 105 Meersseman W, Lagrou K, Maertens J. et al. Galactomannan in bronchoalveolar lavage fluid: a tool for diagnosing aspergillosis in intensive care unit patients. Am J Respir Crit Care Med 2008; 177 (01) 27-34
  • 106 Husain S, Clancy CJ, Nguyen MH. et al. Performance characteristics of the platelia Aspergillus enzyme immunoassay for detection of Aspergillus galactomannan antigen in bronchoalveolar lavage fluid. Clin Vaccine Immunol 2008; 15 (12) 1760-1763
  • 107 Musher B, Fredricks D, Leisenring W, Balajee SA, Smith C, Marr KA. Aspergillus galactomannan enzyme immunoassay and quantitative PCR for diagnosis of invasive aspergillosis with bronchoalveolar lavage fluid. J Clin Microbiol 2004; 42 (12) 5517-5522
  • 108 Maertens J, Maertens V, Theunissen K. et al. Bronchoalveolar lavage fluid galactomannan for the diagnosis of invasive pulmonary aspergillosis in patients with hematologic diseases. Clin Infect Dis 2009; 49 (11) 1688-1693
  • 109 D'Haese J, Theunissen K, Vermeulen E. et al. Detection of galactomannan in bronchoalveolar lavage fluid samples of patients at risk for invasive pulmonary aspergillosis: analytical and clinical validity. J Clin Microbiol 2012; 50 (04) 1258-1263
  • 110 Zou M, Tang L, Zhao S. et al. Systematic review and meta-analysis of detecting galactomannan in bronchoalveolar lavage fluid for diagnosing invasive aspergillosis. PLoS One 2012; 7 (08) e43347
  • 111 Guo YL, Chen YQ, Wang K, Qin SM, Wu C, Kong JL. Accuracy of BAL galactomannan in diagnosing invasive aspergillosis: a bivariate metaanalysis and systematic review. Chest 2010; 138 (04) 817-824
  • 112 Heng SC, Morrissey O, Chen SCA. et al. Utility of bronchoalveolar lavage fluid galactomannan alone or in combination with PCR for the diagnosis of invasive aspergillosis in adult hematology patients: a systematic review and meta-analysis. Crit Rev Microbiol 2015; 41 (01) 124-134
  • 113 Pfeiffer CD, Fine JP, Safdar N. Diagnosis of invasive aspergillosis using a galactomannan assay: a meta-analysis. Clin Infect Dis 2006; 42 (10) 1417-1427
  • 114 Cordonnier C, Botterel F, Ben Amor R. et al. Correlation between galactomannan antigen levels in serum and neutrophil counts in haematological patients with invasive aspergillosis. Clin Microbiol Infect 2009; 15 (01) 81-86
  • 115 Teering S, Verreth A, Peeters A. et al. Prognostic value of serum galactomannan in mixed ICU patients: a retrospective observational study. Anaesthesiol Intensive Ther 2014; 46 (03) 145-154
  • 116 Maertens J, Verhaegen J, Lagrou K, Van Eldere J, Boogaerts M. Screening for circulating galactomannan as a noninvasive diagnostic tool for invasive aspergillosis in prolonged neutropenic patients and stem cell transplantation recipients: a prospective validation. Blood 2001; 97 (06) 1604-1610
  • 117 Leeflang MM, Debets-Ossenkopp YJ, Wang J. et al. Galactomannan detection for invasive aspergillosis in immunocompromised patients. Cochrane Database Syst Rev 2015; 2015 (12) CD007394
  • 118 Arvanitis M, Anagnostou T, Mylonakis E. Galactomannan and polymerase chain reaction-based screening for invasive aspergillosis among high-risk hematology patients: a diagnostic meta-analysis. Clin Infect Dis 2015; 61 (08) 1263-1272
  • 119 Duarte RF, Sánchez-Ortega I, Cuesta I. et al. Serum galactomannan-based early detection of invasive aspergillosis in hematology patients receiving effective antimold prophylaxis. Clin Infect Dis 2014; 59 (12) 1696-1702
  • 120 Buil JB, Huygens S, Dunbar A. et al. Retrospective multicenter evaluation of the VirClia galactomannan antigen assay for the diagnosis of pulmonary aspergillosis with bronchoalveolar lavage fluid samples from patients with hematological disease. J Clin Microbiol 2023; 61 (05) e0004423
  • 121 Calero AL, Alonso R, Gadea I. et al. Comparison of the performance of two galactomannan detection tests: platelia aspergillus ag and aspergillus galactomannan Ag Virclia monotest. Microbiol Spectr 2022; 10 (02) e0262621
  • 122 Sulahian A, Porcher R, Bergeron A. et al. Use and limits of (1-3)-β-d-glucan assay (Fungitell), compared to galactomannan determination (Platelia Aspergillus), for diagnosis of invasive aspergillosis. J Clin Microbiol 2014; 52 (07) 2328-2333
  • 123 Marty FM, Lowry CM, Lempitski SJ, Kubiak DW, Finkelman MA, Baden LR. Reactivity of (1–>3)-β-d-glucan assay with commonly used intravenous antimicrobials. Antimicrob Agents Chemother 2006; 50 (10) 3450-3453
  • 124 Chong GM, van der Beek MT, von dem Borne PA. et al. PCR-based detection of Aspergillus fumigatus Cyp51A mutations on bronchoalveolar lavage: a multicentre validation of the AsperGenius assay® in 201 patients with haematological disease suspected for invasive aspergillosis. J Antimicrob Chemother 2016; 71 (12) 3528-3535
  • 125 Hayette MP, Vaira D, Susin F. et al. Detection of Aspergillus species DNA by PCR in bronchoalveolar lavage fluid. J Clin Microbiol 2001; 39 (06) 2338-2340
  • 126 Tuon FF. A systematic literature review on the diagnosis of invasive aspergillosis using polymerase chain reaction (PCR) from bronchoalveolar lavage clinical samples. Rev Iberoam Micol 2007; 24 (02) 89-94
  • 127 Avni T, Levy I, Sprecher H, Yahav D, Leibovici L, Paul M. Diagnostic accuracy of PCR alone compared to galactomannan in bronchoalveolar lavage fluid for diagnosis of invasive pulmonary aspergillosis: a systematic review. J Clin Microbiol 2012; 50 (11) 3652-3658
  • 128 Sun W, Wang K, Gao W. et al. Evaluation of PCR on bronchoalveolar lavage fluid for diagnosis of invasive aspergillosis: a bivariate metaanalysis and systematic review. PLoS One 2011; 6 (12) e28467
  • 129 Huygens S, Dunbar A, Buil JB. et al. Clinical impact of polymerase chain reaction-based aspergillus and azole resistance detection in invasive aspergillosis: a prospective multicenter study. Clin Infect Dis 2023; 77 (01) 38-45
  • 130 Arvanitis M, Ziakas PD, Zacharioudakis IM, Zervou FN, Caliendo AM, Mylonakis E. PCR in diagnosis of invasive aspergillosis: a meta-analysis of diagnostic performance. J Clin Microbiol 2014; 52 (10) 3731-3742
  • 131 Morton CO, White PL, Barnes RA. et al; EAPCRI. Determining the analytical specificity of PCR-based assays for the diagnosis of IA: What is Aspergillus?. Med Mycol 2017; 55 (04) 402-413
  • 132 White PL, Mengoli C, Bretagne S. et al; European Aspergillus PCR Initiative (EAPCRI). Evaluation of Aspergillus PCR protocols for testing serum specimens. J Clin Microbiol 2011; 49 (11) 3842-3848
  • 133 Rogers TR, Morton CO, Springer J. et al. Combined real-time PCR and galactomannan surveillance improves diagnosis of invasive aspergillosis in high risk patients with haematological malignancies. Br J Haematol 2013; 161 (04) 517-524
  • 134 Aguado JM, Vázquez L, Fernández-Ruiz M. et al; PCRAGA Study Group, ; Spanish Stem Cell Transplantation Group, ; Study Group of Medical Mycology of the Spanish Society of Clinical Microbiology and Infectious Diseases, ; Spanish Network for Research in Infectious Diseases. Serum galactomannan versus a combination of galactomannan and polymerase chain reaction-based Aspergillus DNA detection for early therapy of invasive aspergillosis in high-risk hematological patients: a randomized controlled trial. Clin Infect Dis 2015; 60 (03) 405-414
  • 135 Cruciani M, White PL, Mengoli C. et al; Fungal PCR Initiative. The impact of anti-mould prophylaxis on Aspergillus PCR blood testing for the diagnosis of invasive aspergillosis. J Antimicrob Chemother 2021; 76 (03) 635-638
  • 136 Jenks JD, Gangneux JP, Schwartz IS. et al; European Confederation of Medical Mycology (ECMM) Council Investigators. Diagnosis of breakthrough fungal infections in the clinical mycology laboratory: an ECMM consensus statement. J Fungi (Basel) 2020; 6 (04) 216
  • 137 Blot SI, Taccone FS, Van den Abeele AM. et al; AspICU Study Investigators. A clinical algorithm to diagnose invasive pulmonary aspergillosis in critically ill patients. Am J Respir Crit Care Med 2012; 186 (01) 56-64
  • 138 Verweij PE, Rijnders BJA, Brüggemann RJM. et al. Review of influenza-associated pulmonary aspergillosis in ICU patients and proposal for a case definition: an expert opinion. Intensive Care Med 2020; 46 (08) 1524-1535
  • 139 Verweij PE, Gangneux JP, Bassetti M. et al; European Confederation of Medical Mycology, ; International Society for Human and Animal Mycology, ; European Society for Clinical Microbiology and Infectious Diseases Fungal Infection Study Group, ; ESCMID Study Group for Infections in Critically Ill Patients. Diagnosing COVID-19-associated pulmonary aspergillosis. Lancet Microbe 2020; 1 (02) e53-e55
  • 140 Bassetti M, Azoulay E, Kullberg BJ. et al. EORTC/MSGERC definitions of invasive fungal diseases: summary of activities of the intensive care unit working group. Clin Infect Dis 2021; 72 (suppl 2): S121-S127
  • 141 Koulenti D, Papathanakos G, Blot S. Invasive pulmonary aspergillosis in the ICU: tale of a broadening risk profile. Curr Opin Crit Care 2023; 29 (05) 463-469
  • 142 Gaffney S, Kelly DM, Rameli PM, Kelleher E, Martin-Loeches I. Invasive pulmonary aspergillosis in the intensive care unit: current challenges and best practices. APMIS 2023; 131 (11) 654-667
  • 143 Dellière S, Dudoignon E, Voicu S. et al. Combination of mycological criteria: a better surrogate to identify COVID-19-associated pulmonary aspergillosis patients and evaluate prognosis?. J Clin Microbiol 2022; 60 (03) e0216921
  • 144 Bassetti M, Zuccaro V, Asperges E, Scudeller L, Giacobbe DR. FUNDICU investigators (collaborators). Performance of existing definitions and tests for the diagnosis of invasive aspergillosis in critically ill, non-neutropenic, adult patients: an update including COVID-19 data. J Infect 2022; 85 (05) 573-607
  • 145 Bassetti M, Scudeller L, Giacobbe DR. et al; from the Study Group for Infections in Critically Ill Patients (ESGCIP) and the Fungal Infection Study Group (EFISG) of the European Society of Clinical Microbiology and Infectious Diseases (ESCMID), ; European Society of Intensive Care Medicine (ESICM), ; European Confederation of Medical Mycology (ECMM), ; Mycoses Study Group Education and Research Consortium (MSGERC). Developing definitions for invasive fungal diseases in critically ill adult patients in intensive care units. Protocol of the FUNgal infections Definitions in ICU patients (FUNDICU) project. Mycoses 2019; 62 (04) 310-319
  • 146 Jenks JD, Hoenigl M. Treatment of aspergillosis. J Fungi (Basel) 2018; 4 (03) 98
  • 147 Tissot F, Agrawal S, Pagano L. et al. ECIL-6 guidelines for the treatment of invasive candidiasis, aspergillosis and mucormycosis in leukemia and hematopoietic stem cell transplant patients. Haematologica 2017; 102 (03) 433-444
  • 148 Maertens JA, Raad II, Marr KA. et al. Isavuconazole versus voriconazole for primary treatment of invasive mould disease caused by Aspergillus and other filamentous fungi (SECURE): a phase 3, randomised-controlled, non-inferiority trial. Lancet 2016; 387 (10020): 760-769
  • 149 Cornely OA, Maertens J, Bresnik M. et al; AmBiLoad Trial Study Group. Liposomal amphotericin B as initial therapy for invasive mold infection: a randomized trial comparing a high-loading dose regimen with standard dosing (AmBiLoad trial). Clin Infect Dis 2007; 44 (10) 1289-1297
  • 150 Klatt ME, Eschenauer GA. Review of pharmacologic considerations in the use of azole antifungals in lung transplant recipients. J Fungi (Basel) 2021; 7 (02) 76
  • 151 Zonios D, Yamazaki H, Murayama N. et al. Voriconazole metabolism, toxicity, and the effect of cytochrome P450 2C19 genotype. J Infect Dis 2014; 209 (12) 1941-1948
  • 152 Benitez LL, Carver PL. Adverse effects associated with long-term administration of azole antifungal agents. Drugs 2019; 79 (08) 833-853
  • 153 Cornely OA, Hoenigl M, Lass-Flörl C. et al; Mycoses Study Group Education and Research Consortium (MSG-ERC) and the European Confederation of Medical Mycology (ECMM). Defining breakthrough invasive fungal infection-Position paper of the mycoses study group education and research consortium and the European Confederation of Medical Mycology. Mycoses 2019; 62 (09) 716-729
  • 154 Guegan H, Iriart X, Bougnoux ME, Berry A, Robert-Gangneux F, Gangneux JP. Evaluation of MucorGenius® mucorales PCR assay for the diagnosis of pulmonary mucormycosis. J Infect 2020; 81 (02) 311-317
  • 155 Skiada A, Lanternier F, Groll AH. et al; European Conference on Infections in Leukemia. Diagnosis and treatment of mucormycosis in patients with hematological malignancies: guidelines from the 3rd European Conference on Infections in Leukemia (ECIL 3). Haematologica 2013; 98 (04) 492-504
  • 156 Lestrade PP, Bentvelsen RG, Schauwvlieghe AFAD. et al. Voriconazole resistance and mortality in invasive aspergillosis: a multicenter retrospective cohort study. Clin Infect Dis 2019; 68 (09) 1463-1471
  • 157 Millon L, Caillot D, Berceanu A. et al. Evaluation of serum mucorales polymerase chain reaction (PCR) for the diagnosis of mucormycoses: the MODIMUCOR prospective trial. Clin Infect Dis 2022; 75 (05) 777-785
  • 158 Almyroudis NG, Kontoyiannis DP, Sepkowitz KA, DePauw BE, Walsh TJ, Segal BH. Issues related to the design and interpretation of clinical trials of salvage therapy for invasive mold infection. Clin Infect Dis 2006; 43 (11) 1449-1455
  • 159 Bennett JE. Salvage therapy for aspergillosis. Clin Infect Dis 2005; 41 (suppl 6): S387-S388
  • 160 Marr KA, Schlamm HT, Herbrecht R. et al. Combination antifungal therapy for invasive aspergillosis: a randomized trial. Ann Intern Med 2015; 162 (02) 81-89
  • 161 Maertens J, Raad I, Petrikkos G. et al; Caspofungin Salvage Aspergillosis Study Group. Efficacy and safety of caspofungin for treatment of invasive aspergillosis in patients refractory to or intolerant of conventional antifungal therapy. Clin Infect Dis 2004; 39 (11) 1563-1571
  • 162 Walsh TJ, Hiemenz JW, Seibel NL. et al. Amphotericin B lipid complex for invasive fungal infections: analysis of safety and efficacy in 556 cases. Clin Infect Dis 1998; 26 (06) 1383-1396
  • 163 Kuderer NM, Dale DC, Crawford J, Lyman GH. Impact of primary prophylaxis with granulocyte colony-stimulating factor on febrile neutropenia and mortality in adult cancer patients receiving chemotherapy: a systematic review. J Clin Oncol 2007; 25 (21) 3158-3167
  • 164 Sionov E, Mendlovic S, Segal E. Experimental systemic murine aspergillosis: treatment with polyene and caspofungin combination and G-CSF. J Antimicrob Chemother 2005; 56 (03) 594-597
  • 165 Brummer E, Maqbool A, Stevens DA. In vivo GM-CSF prevents dexamethasone suppression of killing of Aspergillus fumigatus conidia by bronchoalveolar macrophages. J Leukoc Biol 2001; 70 (06) 868-872
  • 166 Price TH, Boeckh M, Harrison RW. et al. Efficacy of transfusion with granulocytes from G-CSF/dexamethasone-treated donors in neutropenic patients with infection. Blood 2015; 126 (18) 2153-2161
  • 167 Wright DG, Robichaud KJ, Pizzo PA, Deisseroth AB. Lethal pulmonary reactions associated with the combined use of amphotericin B and leukocyte transfusions. N Engl J Med 1981; 304 (20) 1185-1189
  • 168 Arnold DE, Chellapandian D, Parikh S. et al. Granulocyte transfusions in patients with chronic granulomatous disease undergoing hematopoietic cell transplantation or gene therapy. J Clin Immunol 2022; 42 (05) 1026-1035
  • 169 Daver N, Kontoyiannis DP. Checkpoint inhibitors and aspergillosis in AML: the double hit hypothesis. Lancet Oncol 2017; 18 (12) 1571-1573
  • 170 International Chronic Granulomatous Disease Cooperative Study Group. A controlled trial of interferon gamma to prevent infection in chronic granulomatous disease. N Engl J Med 1991; 324 (08) 509-516
  • 171 Dignani MC, Rex JH, Chan KW. et al. Immunomodulation with interferon-gamma and colony-stimulating factors for refractory fungal infections in patients with leukemia. Cancer 2005; 104 (01) 199-204
  • 172 Maertens JA, Girmenia C, Brüggemann RJ. et al; European Conference on Infections in Leukaemia (ECIL), a joint venture of the European Group for Blood and Marrow Transplantation (EBMT), the European Organization for Research and Treatment of Cancer (EORTC), the Immunocompromised Host Society (ICHS) and, ; European Conference on Infections in Leukaemia (ECIL), a joint venture of the European Group for Blood and Marrow Transplantation (EBMT), the European Organization for Research and Treatment of Cancer (EORTC), the Immunocompromised Host Society (ICHS) and the European LeukemiaNet (ELN). European guidelines for primary antifungal prophylaxis in adult haematology patients: summary of the updated recommendations from the European Conference on Infections in Leukaemia. J Antimicrob Chemother 2018; 73 (12) 3221-3230
  • 173 Marinelli T, Davoudi S, Foroutan F, Orchanian-Cheff A, Husain S. Antifungal prophylaxis in adult lung transplant recipients: Uncertainty despite 30 years of experience. A systematic review of the literature and network meta-analysis. Transpl Infect Dis 2022; 24 (03) e13832
  • 174 Cornely OA, Maertens J, Winston DJ. et al. Posaconazole vs. fluconazole or itraconazole prophylaxis in patients with neutropenia. N Engl J Med 2007; 356 (04) 348-359
  • 175 Ullmann AJ, Lipton JH, Vesole DH. et al. Posaconazole or fluconazole for prophylaxis in severe graft-versus-host disease. N Engl J Med 2007; 356 (04) 335-347
  • 176 Khatri AM, Natori Y, Anderson A. et al. Breakthrough invasive fungal infections on isavuconazole prophylaxis in hematologic malignancy & hematopoietic stem cell transplant patients. Transpl Infect Dis 2023; e14162: e14162
  • 177 Cidara Therapeutics Inc. A phase 3, multicenter, randomized, double-blind study of the efficacy and safety of rezafungin for injection versus the standard antimicrobial regimen to prevent invasive fungal diseases in adults undergoing allogeneic blood and marrow transplantation (The ReSPECT Study). clinicaltrials.gov; 2023. Accessed January 1, 2023 at: https://clinicaltrials.gov/study/NCT04368559
  • 178 EORTC International Antimicrobial Therapy Cooperative Group. Empiric antifungal therapy in febrile granulocytopenic patients. Am J Med 1989; 86 (6, Pt 1): 668-672
  • 179 Goldberg E, Gafter-Gvili A, Robenshtok E, Leibovici L, Paul M. Empirical antifungal therapy for patients with neutropenia and persistent fever: systematic review and meta-analysis. Eur J Cancer 2008; 44 (15) 2192-2203
  • 180 Cordonnier C, Pautas C, Maury S. et al. Empirical versus preemptive antifungal therapy for high-risk, febrile, neutropenic patients: a randomized, controlled trial. Clin Infect Dis 2009; 48 (08) 1042-1051
  • 181 Girmenia C, Micozzi A, Gentile G. et al. Clinically driven diagnostic antifungal approach in neutropenic patients: a prospective feasibility study. J Clin Oncol 2010; 28 (04) 667-674
  • 182 Pagano L, Caira M, Nosari A. et al; HEMA e-Chart Group. The use and efficacy of empirical versus pre-emptive therapy in the management of fungal infections: the HEMA e-Chart Project. Haematologica 2011; 96 (09) 1366-1370
  • 183 Maertens J, Theunissen K, Verhoef G. et al. Galactomannan and computed tomography-based preemptive antifungal therapy in neutropenic patients at high risk for invasive fungal infection: a prospective feasibility study. Clin Infect Dis 2005; 41 (09) 1242-1250
  • 184 Uneno Y, Imura H, Makuuchi Y, Tochitani K, Watanabe N. Pre-emptive antifungal therapy versus empirical antifungal therapy for febrile neutropenia in people with cancer. Cochrane Database Syst Rev 2022; 11 (11) CD013604
  • 185 Maertens J, Lodewyck T, Donnelly JP. et al; Infectious Diseases Group and the Acute Leukemia Group of the European Organization for Research and Treatment of Cancer. Empiric vs preemptive antifungal strategy in high-risk neutropenic patients on fluconazole prophylaxis: a randomized trial of the European Organization for Research and Treatment of Cancer. Clin Infect Dis 2023; 76 (04) 674-682
  • 186 Schwarzinger M, Sagaon-Teyssier L, Cabaret O, Bretagne S, Cordonnier C. PREVERT Investigators. Performance of serum biomarkers for the early detection of invasive aspergillosis in febrile, neutropenic patients: a multi-state model. PLoS One 2013; 8 (06) e65776
  • 187 Cordonnier C, Rovira M, Maertens J. et al; Voriconazole for Secondary Prophylaxis of Invasive Fungal Infections in Patients With Allogeneic Stem Cell Transplants (VOSIFI) study group, ; Infectious Diseases Working Party, European Group for Blood and Marrow Transplantation. Voriconazole for secondary prophylaxis of invasive fungal infections in allogeneic stem cell transplant recipients: results of the VOSIFI study. Haematologica 2010; 95 (10) 1762-1768
  • 188 de Fabritiis P, Spagnoli A, Di Bartolomeo P. et al. Efficacy of caspofungin as secondary prophylaxis in patients undergoing allogeneic stem cell transplantation with prior pulmonary and/or systemic fungal infection. Bone Marrow Transplant 2007; 40 (03) 245-249
  • 189 Krüger WH, Rüssmann B, de Wit M. et al. Haemopoietic cell transplantation of patients with a history of deep or invasive fungal infection during prophylaxis with liposomal amphotericin B. Acta Haematol 2005; 113 (02) 104-108
  • 190 Segal BH, Herbrecht R, Stevens DA. et al. Defining responses to therapy and study outcomes in clinical trials of invasive fungal diseases: Mycoses Study Group and European Organization for Research and Treatment of Cancer consensus criteria. Clin Infect Dis 2008; 47 (05) 674-683
  • 191 Slavin MA, Chen YC, Cordonnier C. et al. When to change treatment of acute invasive aspergillosis: an expert viewpoint. J Antimicrob Chemother 2021; 77 (01) 16-23
  • 192 Vehreschild JJ, Heussel CP, Groll AH. et al. Serial assessment of pulmonary lesion volume by computed tomography allows survival prediction in invasive pulmonary aspergillosis. Eur Radiol 2017; 27 (08) 3275-3282
  • 193 Miceli MH, Maertens J, Buvé K. et al. Immune reconstitution inflammatory syndrome in cancer patients with pulmonary aspergillosis recovering from neutropenia: proof of principle, description, and clinical and research implications. Cancer 2007; 110 (01) 112-120
  • 194 Mercier T, Guldentops E, Lagrou K, Maertens J. Galactomannan, a surrogate marker for outcome in invasive aspergillosis: finally coming of age. Front Microbiol 2018; 9: 661
  • 195 Mercier T, Wera J, Chai LYA, Lagrou K, Maertens J. A mortality prediction rule for hematology patients with invasive aspergillosis based on serum galactomannan kinetics. J Clin Med 2020; 9 (02) 610
  • 196 Chai LYA, Kullberg BJ, Johnson EM. et al. Early serum galactomannan trend as a predictor of outcome of invasive aspergillosis. J Clin Microbiol 2012; 50 (07) 2330-2336
  • 197 Koo S, Bryar JM, Baden LR, Marty FM. Prognostic features of galactomannan antigenemia in galactomannan-positive invasive aspergillosis. J Clin Microbiol 2010; 48 (04) 1255-1260
  • 198 Neofytos D, Railkar R, Mullane KM. et al. Correlation between circulating fungal biomarkers and clinical outcome in invasive aspergillosis. PLoS One 2015; 10 (06) e0129022
  • 199 Boutboul F, Alberti C, Leblanc T. et al. Invasive aspergillosis in allogeneic stem cell transplant recipients: increasing antigenemia is associated with progressive disease. Clin Infect Dis 2002; 34 (07) 939-943
  • 200 Maertens J, Buvé K, Theunissen K. et al. Galactomannan serves as a surrogate endpoint for outcome of pulmonary invasive aspergillosis in neutropenic hematology patients. Cancer 2009; 115 (02) 355-362
  • 201 Hadrich I, Makni F, Cheikhrouhou F. et al. Clinical utility and prognostic value of galactomannan in neutropenic patients with invasive aspergillosis. Pathol Biol (Paris) 2012; 60 (06) 357-361