Plasma Microbial Cell-free DNA Next-generation Sequencing in the Diagnosis and Management of Febrile Neutropenia.


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:
03 05 2022
Historique:
received: 03 11 2020
pubmed: 20 4 2021
medline: 10 5 2022
entrez: 19 4 2021
Statut: ppublish

Résumé

Standard testing fails to identify a pathogen in most patients with febrile neutropenia (FN). We evaluated the ability of the Karius microbial cell-free DNA sequencing test (KT) to identify infectious etiologies of FN and its impact on antimicrobial management. This prospective study (ClinicalTrials.gov; NCT02912117) enrolled and analyzed 55 patients with FN. Up to 5 blood samples were collected per subject within 24 hours of fever onset (T1) and every 2 to 3 days. KT results were compared with blood culture (BC) and standard microbiological testing (SMT) results. Positive agreement was defined as KT identification of ≥1 isolate also detected by BC. At T1, positive and negative agreement were 90% (9/10) and 31% (14/45), respectively; 61% of KT detections were polymicrobial. Clinical adjudication by 3 independent infectious diseases specialists categorized Karius results as: unlikely to cause FN (N = 0); definite (N = 12): KT identified ≥1 organism also found by SMT within 7 days; probable (N = 19): KT result was compatible with a clinical diagnosis; possible (N = 10): KT result was consistent with infection but not considered a common cause of FN. Definite, probable, and possible cases were deemed true positives. Following adjudication, KT sensitivity and specificity were 85% (41/48) and 100% (14/14), respectively. Calculated time to diagnosis was generally shorter with KT (87%). Adjudicators determined real-time KT results could have allowed early optimization of antimicrobials in 47% of patients, by addition of antibacterials (20%) (mostly against anaerobes [12.7%]), antivirals (14.5%), and/or antifungals (3.6%); and antimicrobial narrowing in 27.3% of cases. NCT02912117. KT shows promise in the diagnosis and treatment optimization of FN.

Sections du résumé

BACKGROUND
Standard testing fails to identify a pathogen in most patients with febrile neutropenia (FN). We evaluated the ability of the Karius microbial cell-free DNA sequencing test (KT) to identify infectious etiologies of FN and its impact on antimicrobial management.
METHODS
This prospective study (ClinicalTrials.gov; NCT02912117) enrolled and analyzed 55 patients with FN. Up to 5 blood samples were collected per subject within 24 hours of fever onset (T1) and every 2 to 3 days. KT results were compared with blood culture (BC) and standard microbiological testing (SMT) results.
RESULTS
Positive agreement was defined as KT identification of ≥1 isolate also detected by BC. At T1, positive and negative agreement were 90% (9/10) and 31% (14/45), respectively; 61% of KT detections were polymicrobial. Clinical adjudication by 3 independent infectious diseases specialists categorized Karius results as: unlikely to cause FN (N = 0); definite (N = 12): KT identified ≥1 organism also found by SMT within 7 days; probable (N = 19): KT result was compatible with a clinical diagnosis; possible (N = 10): KT result was consistent with infection but not considered a common cause of FN. Definite, probable, and possible cases were deemed true positives. Following adjudication, KT sensitivity and specificity were 85% (41/48) and 100% (14/14), respectively. Calculated time to diagnosis was generally shorter with KT (87%). Adjudicators determined real-time KT results could have allowed early optimization of antimicrobials in 47% of patients, by addition of antibacterials (20%) (mostly against anaerobes [12.7%]), antivirals (14.5%), and/or antifungals (3.6%); and antimicrobial narrowing in 27.3% of cases.
CLINICAL TRIALS REGISTRATION
NCT02912117.
CONCLUSION
KT shows promise in the diagnosis and treatment optimization of FN.

Identifiants

pubmed: 33870413
pii: 6236109
doi: 10.1093/cid/ciab324
pmc: PMC9070798
doi:

Substances chimiques

Anti-Bacterial Agents 0
Cell-Free Nucleic Acids 0

Banques de données

ClinicalTrials.gov
['NCT02912117']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1659-1668

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.

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Auteurs

Esther Benamu (E)

School of Medicine, Division of Infectious Diseases, University of Colorado Denver, Aurora, Colorado, USA.

Kiran Gajurel (K)

Division of Infectious Diseases, Carolinas Medical Center, Atrium Health, Charlotte, North Carolina, USA.

Jill N Anderson (JN)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

Tullia Lieb (T)

Hematopoietic Malignancies Unit Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California, USA.

Carlos A Gomez (CA)

Division of Infectious Diseases, Department of Medicine, University of Utah, Salt Lake City, Utah, USA.

Hon Seng (H)

Cytovale, Inc., San Francisco, California, USA.

Romielle Aquino (R)

Karius, Inc., Redwood City, California, USA.

Desiree Hollemon (D)

Karius, Inc., Redwood City, California, USA.

David K Hong (DK)

Vir Biotechnology Inc., San Francisco, California, USA.

Timothy A Blauwkamp (TA)

Karius, Inc., Redwood City, California, USA.

Mickey Kertesz (M)

Karius, Inc., Redwood City, California, USA.

Lily Blair (L)

Karius, Inc., Redwood City, California, USA.

Paul L Bollyky (PL)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

Bruno C Medeiros (BC)

Division of Hematology, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

Steven Coutre (S)

Division of Hematology, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

Simona Zompi (S)

Sangamo Therapeutics Inc, Brisbane, California, USA.

Jose G Montoya (JG)

The Dr. Jack S. Remington Laboratory for Specialty Diagnostics at the Palo Alto Medical Foundation, Palo Alto, California, USA.

Stan Deresinski (S)

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.

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Classifications MeSH