Evaluation of Serum Mucorales Polymerase Chain Reaction (PCR) for the Diagnosis of Mucormycoses: The MODIMUCOR Prospective Trial.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
14 09 2022
Historique:
received: 09 08 2021
pubmed: 6 1 2022
medline: 20 9 2022
entrez: 5 1 2022
Statut: ppublish

Résumé

Early diagnosis and prompt initiation of specific antifungal treatment are essential for improving the prognosis of mucormycosis. We aimed to assess the performance of serum Mucorales quantitative polymerase chain reaction (qPCR) for the early diagnosis and follow-up of mucormycosis. We prospectively enrolled 232 patients with suspicion of invasive mold disease, evaluated using standard imaging and mycological procedures. Thirteen additional patients with proven or probable mucormycosis were included to analyze DNA load kinetics. Serum samples were collected twice-a-week for Mucorales qPCR tests targeting the Mucorales genera Lichtheimia, Rhizomucor, and Mucor/Rhizopus. The sensitivity was 85.2%, specificity 89.8%, and positive and negative likelihood ratios 8.3 and 0.17, respectively in this prospective study. The first Mucorales qPCR-positive serum was observed a median of 4 days (interquartile range [IQR], 0-9) before sampling of the first mycological or histological positive specimen and a median of one day (IQR, -2 to 6) before the first imaging was performed. Negativity of Mucorales qPCR within seven days after liposomal-amphotericin B initiation was associated with an 85% lower 30-day mortality rate (adjusted hazard ratio = 0·15, 95% confidence interval [.03-.73], P = .02). Our study argues for the inclusion of qPCR for the detection of circulating Mucorales DNA for mucormycosis diagnosis and follow-up after treatment initiation. Positive results should be added to the criteria for the consensual definitions from the European Organization for the Research and Treatment of Cancer/Mycoses Study Group Education and Research Consortium (EORTC/MSGERC), as already done for Aspergillus PCR.

Sections du résumé

BACKGROUND
Early diagnosis and prompt initiation of specific antifungal treatment are essential for improving the prognosis of mucormycosis. We aimed to assess the performance of serum Mucorales quantitative polymerase chain reaction (qPCR) for the early diagnosis and follow-up of mucormycosis.
METHODS
We prospectively enrolled 232 patients with suspicion of invasive mold disease, evaluated using standard imaging and mycological procedures. Thirteen additional patients with proven or probable mucormycosis were included to analyze DNA load kinetics. Serum samples were collected twice-a-week for Mucorales qPCR tests targeting the Mucorales genera Lichtheimia, Rhizomucor, and Mucor/Rhizopus.
RESULTS
The sensitivity was 85.2%, specificity 89.8%, and positive and negative likelihood ratios 8.3 and 0.17, respectively in this prospective study. The first Mucorales qPCR-positive serum was observed a median of 4 days (interquartile range [IQR], 0-9) before sampling of the first mycological or histological positive specimen and a median of one day (IQR, -2 to 6) before the first imaging was performed. Negativity of Mucorales qPCR within seven days after liposomal-amphotericin B initiation was associated with an 85% lower 30-day mortality rate (adjusted hazard ratio = 0·15, 95% confidence interval [.03-.73], P = .02).
CONCLUSIONS
Our study argues for the inclusion of qPCR for the detection of circulating Mucorales DNA for mucormycosis diagnosis and follow-up after treatment initiation. Positive results should be added to the criteria for the consensual definitions from the European Organization for the Research and Treatment of Cancer/Mycoses Study Group Education and Research Consortium (EORTC/MSGERC), as already done for Aspergillus PCR.

Identifiants

pubmed: 34986227
pii: 6497755
doi: 10.1093/cid/ciab1066
doi:

Substances chimiques

Antifungal Agents 0
Amphotericin B 7XU7A7DROE

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

777-785

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Potential conflicts of interests. L. M. reports personal fees outside the submitted work and travel grants from Gilead and Pfizer. S. B. reports personal fees outside the submitted work and travel grants from Gilead. F. L. reports personal fees from Airnspace, Gilead, and F2G outside the submitted work. A. A. reports personal fees form Gilead and Pfizer outside the submitted work, consulting fees from Pfizer for serving on an Advisory Board; travel grants from Gilead and Pfizer; and patent licensed for Pneumocystis PCR and patent issued for Histoplasma PCR. F. D. reports travel grants from Pfizer to attend Trend in Medical Mycology congress, Aberdeen, 2021 and is Vice President for French Society of Medical Mycology. R. H. reports research grant from Gilead, personal fees form Gilead and Pfizer outside the submitted work, and travel grants from Gilead and Pfizer. A. P. B. reports support for attending meetings and/or travel from Gilead. BD reports fees for travel and as a speaker at 2 national congresses in 2021 from Gilead and consultancy fees at an expert meeting planned in 01/2022 from Pfizer. F. B. reports consulting fees, payment or honoraria, and support for attending meetings and/or travel from Gilead and support for attending meetings and/or travel from Pfizer and leadership or fiduciary role from the Society of French Medical Mycology. S. B. reports honorarium from Gilead to attend an educational workshop and support for attending meetings and/or travel from Gilead travel grant for TIMM congress Aberdeen UK. 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.

Auteurs

Laurence Millon (L)

Laboratoire de Parasitologie-Mycologie, Centre hospitalier universtaire (CHU) Besançon, Besançon, France.
Unité mixte de recherche (UMR) 6249 Centre national de la recherche scientifique (CNRS) Chrono-Environnement, Univ Bourgogne Franche-Comté, Besançon, France.

Denis Caillot (D)

Department of Clinical Hematology, CHU Dijon, Dijon, France.

Ana Berceanu (A)

Service d'Hematologie, CHU Besançon, Besançon, France.

Stéphane Bretagne (S)

Institut Pasteur, CNRS, Molecular Mycology Unit, National Reference Center for Invasive Mycoses and Antifungals, UMR 2000, Paris, France.
Laboratoire de Parasitologie-Mycologie, Hôpital Saint Louis, AP-HP, Paris, France.
Université de Paris, Paris, France.

Fanny Lanternier (F)

Institut Pasteur, CNRS, Molecular Mycology Unit, National Reference Center for Invasive Mycoses and Antifungals, UMR 2000, Paris, France.
Université de Paris, Paris, France.
Necker Pasteur Center for Infectious Diseases and Tropical Medicine, Hôpital Necker Enfants malades, AP-HP, Instituts Hôpitaux Universitaires (IHU) Imagine, Paris, France.

Florent Morio (F)

Laboratoire de Parasitologie-Mycologie, CHU Nantes, Nantes, France.
Département de Parasitologie et Mycologie Médicale, EA1155 - IICiMed, Nantes Université, Nantes, France.

Valérie Letscher-Bru (V)

Laboratoire de Parasitologie et de Mycologie Médicale, Hôpitaux Universitaires de Strasbourg, France.

Frédéric Dalle (F)

Laboratoire de Parasitologie-Mycologie, Plateforme de Biologie Hospitalo-Universitaire Gérard Mack, Dijon, France.
UMR PAM Univ Bourgogne Franche-Comté, AgroSup Dijon, Equipe Vin, Aliment, Microbiologie, Stress, Dijon, France.

Blandine Denis (B)

Infectious Diseases Department, APHP, Saint-Louis Hospital, Paris, France.

Alexandre Alanio (A)

Institut Pasteur, CNRS, Molecular Mycology Unit, National Reference Center for Invasive Mycoses and Antifungals, UMR 2000, Paris, France.
Laboratoire de Parasitologie-Mycologie, Hôpital Saint Louis, AP-HP, Paris, France.
Université de Paris, Paris, France.

David Boutoille (D)

Unité Maladies Infectieuses et Tropicales, CHU Nantes, Nantes, France.

Marie Elisabeth Bougnoux (ME)

Parasitology-Mycology Unit, Necker Enfants Malades Hospital, APHP, Paris, France.
Fungal Biology and Pathogenicity Unit, INRA USC 2019, Institut Pasteur, Paris, France.

Françoise Botterel (F)

EA Dynamyc 7380 UPEC, ENVA, Faculté de Médecine, Créteil, France.
Unité de Parasitologie, Mycologie, Département de Virologie, Bactériologie-Hygiène, Mycologie-Parasitologie, DHU VIC, CHU Henri Mondor, Créteil, France.

Taieb Chouaki (T)

Laboratoire de Parasitologie et Mycologie Médicales, Centre de Biologie Humaine, CHU Amiens Picardie, Amiens, France.
Equipe AGIR: Agents Infectieux, Résistance et Chimiothérapie UR4294, Université de Picardie Jules Verne, Amiens, France.

Amandine Charbonnier (A)

Department of Clinical Hematology and Cellular Therapy, Amiens University Medical Center, Amiens, France.

Florence Ader (F)

Hospices Civils de Lyon, Département des Maladies Infectieuses et Tropicales, F-69004, Lyon, France.

Damien Dupont (D)

Institut des Agents Infectieux, Parasitologie Mycologie, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, Lyon, France.

Anne Pauline Bellanger (AP)

Laboratoire de Parasitologie-Mycologie, Centre hospitalier universtaire (CHU) Besançon, Besançon, France.
Unité mixte de recherche (UMR) 6249 Centre national de la recherche scientifique (CNRS) Chrono-Environnement, Univ Bourgogne Franche-Comté, Besançon, France.

Steffi Rocchi (S)

Laboratoire de Parasitologie-Mycologie, Centre hospitalier universtaire (CHU) Besançon, Besançon, France.
Unité mixte de recherche (UMR) 6249 Centre national de la recherche scientifique (CNRS) Chrono-Environnement, Univ Bourgogne Franche-Comté, Besançon, France.

Emeline Scherer (E)

Laboratoire de Parasitologie-Mycologie, Centre hospitalier universtaire (CHU) Besançon, Besançon, France.
Unité mixte de recherche (UMR) 6249 Centre national de la recherche scientifique (CNRS) Chrono-Environnement, Univ Bourgogne Franche-Comté, Besançon, France.

Houssein Gbaguidi-Haore (H)

Unité mixte de recherche (UMR) 6249 Centre national de la recherche scientifique (CNRS) Chrono-Environnement, Univ Bourgogne Franche-Comté, Besançon, France.
Infection Control Department, CHU Besançon, Besançon, France.

Raoul Herbrecht (R)

Université de Strasbourg, INSERM, IRFAC UMR-S1113, Strasbourg, Franceand.
Service d'Hématologie, Institut de Cancérologie Strasbourg Europe (ICANS), Strasbourg, France.

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