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      Clinical Impact of Polymerase Chain Reaction–Based Aspergillus and Azole Resistance Detection in Invasive Aspergillosis: A Prospective Multicenter Study

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      , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , ,
      Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
      Oxford University Press
      invasive aspergillosis, azole resistance, Aspergillus PCR , clinical impact

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          Abstract

          Background

          Invasive aspergillosis (IA) by a triazole-resistant Aspergillus fumigatus is associated with high mortality. Real-time resistance detection will result in earlier initiation of appropriate therapy.

          Methods

          In a prospective study, we evaluated the clinical value of the AsperGenius polymerase chain reaction (PCR) assay in hematology patients from 12 centers. This PCR assay detects the most frequent cyp51A mutations in A. fumigatus conferring azole resistance. Patients were included when a computed tomography scan showed a pulmonary infiltrate and bronchoalveolar fluid (BALf) sampling was performed. The primary end point was antifungal treatment failure in patients with azole-resistant IA.

          Results

          Of 323 patients enrolled, complete mycological and radiological information was available for 276 (94%), and probable IA was diagnosed in 99/276 (36%). Sufficient BALf for PCR testing was available for 293/323 (91%). Aspergillus DNA was detected in 116/293 (40%) and A. fumigatus DNA in 89/293 (30%). The resistance PCR was conclusive in 58/89 (65%) and resistance detected in 8/58 (14%). Two had a mixed azole-susceptible/azole-resistant infection. In the 6 remaining patients, treatment failure was observed in 1. Galactomannan positivity was associated with mortality ( P = .004) while an isolated positive Aspergillus PCR was not ( P = .83).

          Conclusions

          Real-time PCR-based resistance testing may help to limit the clinical impact of triazole resistance. In contrast, the clinical impact of an isolated positive Aspergillus PCR on BALf seems limited. The interpretation of the EORTC/MSGERC PCR criterion for BALf may need further specification (eg, minimum cycle threshold value and/or PCR positive on >1 BALf sample).

          Abstract

          This prospective multicenter study showed that real-time resistance testing may limit the impact of azole resistance on mortality. An isolated positive polymerase chain reaction assay was not associated with mortality. Its place in the current EORTC/MSGERC definitions should be reconsidered.

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          Most cited references14

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          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

          Abstract Background Invasive fungal diseases (IFDs) remain important causes of morbidity and mortality. The consensus definitions of the Infectious Diseases Group of the European Organization for Research and Treatment of Cancer and the Mycoses Study Group have been of immense value to researchers who conduct clinical trials of antifungals, assess diagnostic tests, and undertake epidemiologic studies. However, their utility has not extended beyond patients with cancer or recipients of stem cell or solid organ transplants. With newer diagnostic techniques available, it was clear that an update of these definitions was essential. Methods To achieve this, 10 working groups looked closely at imaging, laboratory diagnosis, and special populations at risk of IFD. A final version of the manuscript was agreed upon after the groups’ findings were presented at a scientific symposium and after a 3-month period for public comment. There were several rounds of discussion before a final version of the manuscript was approved. Results There is no change in the classifications of “proven,” “probable,” and “possible” IFD, although the definition of “probable” has been expanded and the scope of the category “possible” has been diminished. The category of proven IFD can apply to any patient, regardless of whether the patient is immunocompromised. The probable and possible categories are proposed for immunocompromised patients only, except for endemic mycoses. Conclusions These updated definitions of IFDs should prove applicable in clinical, diagnostic, and epidemiologic research of a broader range of patients at high-risk.
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            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.

            Isavuconazole is a novel triazole with broad-spectrum antifungal activity. The SECURE trial assessed efficacy and safety of isavuconazole versus voriconazole in patients with invasive mould disease.
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              Voriconazole versus amphotericin B for primary therapy of invasive aspergillosis.

              Voriconazole is a broad-spectrum triazole that is active against aspergillus species. We conducted a randomized trial to compare voriconazole with amphotericin B for primary therapy of invasive aspergillosis. In this randomized, unblinded trial, patients received either intravenous voriconazole (two doses of 6 mg per kilogram of body weight on day 1, then 4 mg per kilogram twice daily for at least seven days) followed by 200 mg orally twice daily or intravenous amphotericin B deoxycholate (1 to 1.5 mg per kilogram per day). Other licensed antifungal treatments were allowed if the initial therapy failed or if the patient had an intolerance to the first drug used. A complete or partial response was considered to be a successful outcome. A total of 144 patients in the voriconazole group and 133 patients in the amphotericin B group with definite or probable aspergillosis received at least one dose of treatment. In most of the patients, the underlying condition was allogeneic hematopoietic-cell transplantation, acute leukemia, or other hematologic diseases. At week 12, there were successful outcomes in 52.8 percent of the patients in the voriconazole group (complete responses in 20.8 percent and partial responses in 31.9 percent) and 31.6 percent of those in the amphotericin B group (complete responses in 16.5 percent and partial responses in 15.0 percent; absolute difference, 21.2 percentage points; 95 percent confidence interval, 10.4 to 32.9). The survival rate at 12 weeks was 70.8 percent in the voriconazole group and 57.9 percent in the amphotericin B group (hazard ratio, 0.59; 95 percent confidence interval, 0.40 to 0.88). Voriconazole-treated patients had significantly fewer severe drug-related adverse events, but transient visual disturbances were common with voriconazole (occurring in 44.8 percent of patients). In patients with invasive aspergillosis, initial therapy with voriconazole led to better responses and improved survival and resulted in fewer severe side effects than the standard approach of initial therapy with amphotericin B. Copyright 2002 Massachusetts Medical Society
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                Author and article information

                Contributors
                Journal
                Clin Infect Dis
                Clin Infect Dis
                cid
                Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
                Oxford University Press (US )
                1058-4838
                1537-6591
                01 July 2023
                11 March 2023
                11 March 2023
                : 77
                : 1
                : 38-45
                Affiliations
                Department of Internal Medicine, Section of Infectious Diseases and Department of Medical Microbiology and Infectious Diseases, Erasmus MC, University Medical Center , Rotterdam, The Netherlands
                Department of Internal Medicine, Section of Infectious Diseases and Department of Medical Microbiology and Infectious Diseases, Erasmus MC, University Medical Center , Rotterdam, The Netherlands
                Department of Medical Microbiology, Radboud University Center , Nijmegen, The Netherlands
                Department of Medical Microbiology & Infectious Diseases, Erasmus MC, University Medical Center , Rotterdam, The Netherlands
                Department of Medical Microbiology, Radboud University Center , Nijmegen, The Netherlands
                Department of Medical Microbiology, Amsterdam University Medical Centers , Amsterdam, The Netherlands
                Department of Hematology, Amsterdam University Medical Centers , Amsterdam, The Netherlands
                Department of Hematology, Amsterdam University Medical Centers , Amsterdam, The Netherlands
                Department of Hematology, Radboud University Center , Nijmegen, The Netherlands
                Department of Hematology, Amsterdam University Medical Centers , Amsterdam, The Netherlands
                Department of Medical Microbiology, Amsterdam University Medical Centers , Amsterdam, The Netherlands
                Department of Internal Medicine, Infectious Diseases, University Medical Center Utrecht , The Netherlands
                Department of Medical Microbiology, University Medical Center Utrecht , The Netherlands
                Department of Hematology, Maastricht University Medical Center , The Netherlands
                Department of Medical Microbiology, Maastricht University Medical Center , The Netherlands
                Department of Medical Microbiology, Leiden University Medical Center , The Netherlands
                Department of Hematology, Leiden University Medical Center , The Netherlands
                Department of Hematology, Meander Medical Center , Amersfoort, The Netherlands
                Department of Hematology, University Medical Center Groningen , The Netherlands
                Department of Medical Microbiology, Meander Medical Center , Amersfoort, The Netherlands
                Department of Hematology, University Medical Center Groningen , The Netherlands
                Department of Internal Medicine and Infectious Diseases, University Medical Center Groningen , The Netherlands
                Department of Medical Microbiology, University of Groningen, University Medical Center Groningen , The Netherlands
                Department of Hematology, University Hospitals Leuven , Leuven, Belgium
                Department of Microbiology, Immunology and Transplantation, KU Leuven , Leuven, Belgium
                Department of Microbiology, Immunology and Transplantation, KU Leuven , Leuven, Belgium
                Department of Laboratory Medicine and National Reference Centre for Mycosis, University Hospitals Leuven , Leuven, Belgium
                Department of Hematology, University Hospitals Leuven , Leuven, Belgium
                Department of Microbiology, Immunology and Transplantation, KU Leuven , Leuven, Belgium
                Department of Hematology, Ghent University Hospital , Ghent, Belgium
                Department of Medical Microbiology, Ghent University Hospital , Ghent, Belgium
                Department of Hematology, AZ St-Jan Brugge-Oostende Hospital , Bruges, Belgium
                Department of Laboratory Medicine, Medical Microbiology, AZ St-Jan Brugge-Oostende Hospital , Bruges, Belgium
                Department of Medical Microbiology & Infectious Diseases, Erasmus MC, University Medical Center , Rotterdam, The Netherlands
                Department of Hematology, Erasmus University Medical Center , Rotterdam, The Netherlands
                Department of Hematology, Erasmus University Medical Center , Rotterdam, The Netherlands
                Department of Hematology, AZ St-Jan Brugge-Oostende Hospital , Bruges, Belgium
                Department of Internal Medicine, Section of Infectious Diseases and Department of Medical Microbiology and Infectious Diseases, Erasmus MC, University Medical Center , Rotterdam, The Netherlands
                Author notes

                S. H. and A. D. contributed equally to this work.

                Correspondence: B. J. A. Rijnders, Department of Internal Medicine, Section of Infectious Diseases and Department of Medical Microbiology and Infectious Diseases, Erasmus MC, University Medical Center, Dr. Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands ( b.rijnders@ 123456erasmusmc.nl ).

                Potential conflicts of interest J. M. reports grants from Gilead Sciences, Inc; consulting fees, payment for lectures/presentations, and support for meetings/travel expenses from Gilead Sciences, Inc, MSD, Pfizer, Takeda, and F2G; and participation on a data safety monitoring board or advisory board for Gilead Sciences, Inc, MSD, Pfizer, Takeda, F2G, and Cidara. P. G. reports partial support for travel to Trends In Medical Mycology conference. K. L. reports grants from Thermo Fisher Scientific and TECOmedical paid to their institution; consulting fees from Gilead, MSD, and MRM Health, all paid to their institution; and personal fees for lectures/presentations for Pfizer, Gilead, and FUJIFILM Wako. M. R. reports support for travel to Trends In Medical Mycology conference. J. J. reports grants from Novartis and BMS, both paid to their institution; payment for lectures from AbbVie, Novartis, Pfizer, and Incyte; and serving as president of the Apps for Care and Science, a nonprofit organization, supported by AbbVie, Alexion, Amgen, Astellas, BMS, Daiichi-Sankyo, Janssen-Cilag, Olympus, Incyte, Sanofi Genzyme, Servier, Jazz, and Takeda. J. B. reports research grants from Gilead Sciences, Inc, and F2G. P. V. reports research grants from F2G and Gilead, paid to their institution; honoraria for lectures from F2G, Gilead, and Pfizer, all paid to their institution; and participation on a data safety monitoring board for F2G, paid to their institution. S. H. reports support from Gilead for travel to the International Society for Human and Animal Mycology 2022 conference. B. R. reports research grants from Gilead Sciences, Inc; support for meetings/travel expenses from Gilead Sciences, Inc, F2G, and Pfizer; consulting fees from F2G; payment/honoraria for lectures/presentations from Gilead Sciences, Inc; and participation on a data safety monitoring board/advisory board for Exevir. All other authors report no potential conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

                Author information
                https://orcid.org/0000-0002-9418-8256
                https://orcid.org/0000-0003-3343-9610
                Article
                ciad141
                10.1093/cid/ciad141
                10320047
                36905147
                effc6331-ad7b-4475-8867-e9aba30f7540
                © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 14 November 2022
                : 06 March 2023
                : 18 May 2023
                Page count
                Pages: 8
                Funding
                Funded by: Gilead Sciences, Inc, DOI 10.13039/100005564;
                Award ID: IN-NL-131-4187
                Categories
                Major Article
                Original Article
                AcademicSubjects/MED00290

                Infectious disease & Microbiology
                invasive aspergillosis,azole resistance, aspergillus pcr,clinical impact

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