Approach for defining human adenovirus infection and disease for central review adjudication in clinical studies

Author:

Fisher Brian T.12ORCID,Blumenstock Jesse1,Boge Craig L. K.1,Shuster Sydney1,Seif Alix E.3,Green Michael4ORCID,Michaels Marian G.4,Alexander Jessie L.5,Ardura Monica I.67,Miller Tamara P.89,Hijano Diego R.10ORCID,Muller William J.1112ORCID,Schuster Jennifer E.13ORCID,Green Abby M.14,Dulek Daniel E.1516ORCID,Kajon Adriana E.17,Danziger‐Isakov Lara1819ORCID

Affiliation:

1. Division of Infectious Diseases Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

2. Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

3. Section of of Cellular Therapy and Transplantation in the Division of Oncology Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

4. Division of Infectious Diseases UPMC Children's Hospital of Pittsburgh Pittsburgh Pennsylvania USA

5. Division of Pediatric Stem Cell Transplantation and Cellular Therapies UPMC Children's Hospital of Pittsburgh Pittsburgh Pennsylvania USA

6. Nationwide Children's Hospital Columbus Ohio USA

7. The Ohio State University Columbus Ohio USA

8. Children's Healthcare of Atlanta Atlanta Georgia USA

9. Emory University School of Medicine Atlanta Georgia USA

10. St. Jude Children's Research Hospital Memphis Tennessee USA

11. Ann & Robert H. Lurie Children's Hospital of Chicago Chicago Illinois USA

12. Northwestern University Feinberg School of Medicine Chicago Illinois USA

13. Children's Mercy Kansas City Kansas City Missouri USA

14. Washington University School of Medicine St. Louis Missouri USA

15. Monroe Carell Jr. Children's Hospital at Vanderbilt Nashville Tennessee USA

16. Vanderbilt University Medical Center Nashville Tennessee USA

17. Infectious Disease Program Lovelace Biomedical Research Institute Albuquerque New Mexico USA

18. Cincinnati Children's Hospital Medical Center Cincinnati Ohio USA

19. University of Cincinnati Cincinnati Ohio USA

Abstract

AbstractBackgroundPediatric allogeneic hematopoietic cell transplant (allo‐HCT) recipients are at risk for morbidity and mortality from human adenovirus (HAdV). HAdV can be detected in an asymptomatic state, referred to as infection or with signs or symptoms of illness, referred to as disease. Standardized case definitions are needed to distinguish infection from disease and allow for consistent reporting in both observational cohort studies and therapeutic clinical trials.MethodsA working group of experts in virology, transplant infectious disease, and HCT was assembled to develop HAdV infection and disease definitions with the degree of certainty (i.e., possible, probable, and proven). Definitions were further refined through an iterative process and independently applied by two central review committees (CRCs) to 20 pediatric allo‐HCT recipients with at least one HAdV‐positive PCR.ResultsInitial HAdV infection and disease definitions were developed and updated through an iterative process after reviewing clinical and virological details for 81 subjects with at least one positive HAdV PCR detected in a clinical specimen. Independent application of final definitions to 20 HAdV positive allo‐HCT recipients by two CRCs yielded similar number of HAdV infection or disease events but with variation of degree of certainty for some events.ConclusionsApplication of definitions by a CRC for a study of HAdV infection and disease is feasible and can provide consistency in the assignment of outcomes. Definitions need further refinement to improve reproducibility and to provide guidance on determining clinical improvement or worsening after initial diagnosis of HAdV infection or disease.

Funder

National Institute of Allergy and Infectious Diseases

U.S. Food and Drug Administration

Publisher

Wiley

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