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

被引:87
作者
Benamu, Esther [1 ]
Gajurel, Kiran [2 ]
Anderson, Jill N. [3 ]
Lieb, Tullia [4 ]
Gomez, Carlos A. [5 ]
Seng, Hon [6 ]
Aquino, Romielle [7 ]
Hollemon, Desiree [7 ]
Hong, David K. [8 ]
Blauwkamp, Timothy A. [7 ]
Kertesz, Mickey [7 ]
Blair, Lily [7 ]
Bollyky, Paul L. [3 ]
Medeiros, Bruno C. [9 ]
Coutre, Steven [9 ]
Zompi, Simona [10 ]
Montoya, Jose G. [11 ]
Deresinski, Stan [3 ]
机构
[1] Univ Colorado Denver, Sch Med, Div Infect Dis, Aurora, CO USA
[2] Atrium Hlth, Div Infect Dis, Carolinas Med Ctr, Charlotte, NC USA
[3] Stanford Univ, Dept Med, Div Infect Dis & Geog Med, Sch Med, Stanford, CA 94305 USA
[4] Univ Calif San Francisco, Hematopoiet Malignancies Unit, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[5] Univ Utah, Dept Med, Div Infect Dis, Salt Lake City, UT 84112 USA
[6] Cytovale Inc, San Francisco, CA USA
[7] Karius Inc, Redwood City, CA USA
[8] Vir Biotechnol Inc, San Francisco, CA USA
[9] Stanford Univ, Dept Med, Div Hematol, Sch Med, Stanford, CA 94305 USA
[10] Sangamo Therapeut Inc, Brisbane, CA USA
[11] Palo Alto Med Fdn, Dr Jack S Remington Lab Specialty Diagnost, Palo Alto, CA USA
关键词
Febrile neutropenia; infection; next-generation sequencing; INFECTIONS;
D O I
10.1093/cid/ciab324
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. Conclusion KT shows promise in the diagnosis and treatment optimization of FN. Microbial cell-free DNA sequencing using the Karius test (KT) detects organisms not identified by conventional microbiological tests. KT can be useful in the etiologic diagnosis of infection of febrile neutropenia and may facilitate prompt and optimal antimicrobial therapy.
引用
收藏
页码:1659 / 1668
页数:10
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