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51. A Review of Human Herpesvirus 6 and Central Nervous System Disease in Oncology Patients

BACKGROUND: Human herpesvirus 6 (HHV-6) infects most of the human population. With immunosuppression it can reactivate and cause clinical syndromes of central nervous system (CNS) dysfunction. Much of the literature describes cases after hematopoietic stem cell transplantation (HSCT), ranging from e...

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Autores principales: Handley, Guy H, Hasbun, Rodrigo, Okhuysen, Pablo C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777935/
http://dx.doi.org/10.1093/ofid/ofaa439.361
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author Handley, Guy H
Hasbun, Rodrigo
Okhuysen, Pablo C
author_facet Handley, Guy H
Hasbun, Rodrigo
Okhuysen, Pablo C
author_sort Handley, Guy H
collection PubMed
description BACKGROUND: Human herpesvirus 6 (HHV-6) infects most of the human population. With immunosuppression it can reactivate and cause clinical syndromes of central nervous system (CNS) dysfunction. Much of the literature describes cases after hematopoietic stem cell transplantation (HSCT), ranging from encephalitis to a defined post-transplant acute limbic encephalitis syndrome (PALE). Outside of HSCT, studies of HHV-6 encephalitis in cancer patients are limited to case reports. METHODS: In this retrospective review, we present data from all patients admitted to MD Anderson Cancer Center between March 2016 and December 2018 that met established definitions for encephalitis, aseptic meningitis or HHV-6 PALE with detectable HHV-6 DNA in the cerebrospinal fluid (CSF) detected using either the Viracor or Biofire® Meningitis Encephalitis (ME) Panel testing platforms and no other identified etiology. We extracted demographic features, known risk factors, imaging findings, CSF analysis, treatments and patient outcomes from medical records. RESULTS: 725 patients underwent HHV-6 testing during the study timeframe, with 19 (2.6%) cases of HHV-6 mediated CNS disease identified. Most patients, 13/19 (68%), had undergone HSCT. Median time to presentation was 31 days post-transplant. Survival at 240 days after transplant was 62% often with long-term neurologic sequelae. CSF tended to have lymphocyte predominance and nearly all patients had peripheral lymphopenia. Other at risk populations identified included 2/19 (11%) patients who received chimeric antigen receptor (CAR) T-cell therapy, 2/19 (11%) who received biologic immunotherapy, and 2/19 (11%) who had non-HSCT hematologic malignancy. Notable discordance among testing platforms was found in 5/9 (55%) of patients receiving both testing platforms. CSF and Laboratory Analytes [Image: see text] Findings and Outcomes in HSCT Patients [Image: see text] Findings and Outcomes in Non-HSCT Patients [Image: see text] CONCLUSION: In addition to HSCT patients, HHV-6 reactivation leading to CNS disease also occurs in settings such as following adoptive T cell therapy or biologic immunotherapy. Significant diagnostic discordance exists between testing platforms. DISCLOSURES: Rodrigo Hasbun, MD, MPH, Biofire (Consultant)
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spelling pubmed-77779352021-01-07 51. A Review of Human Herpesvirus 6 and Central Nervous System Disease in Oncology Patients Handley, Guy H Hasbun, Rodrigo Okhuysen, Pablo C Open Forum Infect Dis Poster Abstracts BACKGROUND: Human herpesvirus 6 (HHV-6) infects most of the human population. With immunosuppression it can reactivate and cause clinical syndromes of central nervous system (CNS) dysfunction. Much of the literature describes cases after hematopoietic stem cell transplantation (HSCT), ranging from encephalitis to a defined post-transplant acute limbic encephalitis syndrome (PALE). Outside of HSCT, studies of HHV-6 encephalitis in cancer patients are limited to case reports. METHODS: In this retrospective review, we present data from all patients admitted to MD Anderson Cancer Center between March 2016 and December 2018 that met established definitions for encephalitis, aseptic meningitis or HHV-6 PALE with detectable HHV-6 DNA in the cerebrospinal fluid (CSF) detected using either the Viracor or Biofire® Meningitis Encephalitis (ME) Panel testing platforms and no other identified etiology. We extracted demographic features, known risk factors, imaging findings, CSF analysis, treatments and patient outcomes from medical records. RESULTS: 725 patients underwent HHV-6 testing during the study timeframe, with 19 (2.6%) cases of HHV-6 mediated CNS disease identified. Most patients, 13/19 (68%), had undergone HSCT. Median time to presentation was 31 days post-transplant. Survival at 240 days after transplant was 62% often with long-term neurologic sequelae. CSF tended to have lymphocyte predominance and nearly all patients had peripheral lymphopenia. Other at risk populations identified included 2/19 (11%) patients who received chimeric antigen receptor (CAR) T-cell therapy, 2/19 (11%) who received biologic immunotherapy, and 2/19 (11%) who had non-HSCT hematologic malignancy. Notable discordance among testing platforms was found in 5/9 (55%) of patients receiving both testing platforms. CSF and Laboratory Analytes [Image: see text] Findings and Outcomes in HSCT Patients [Image: see text] Findings and Outcomes in Non-HSCT Patients [Image: see text] CONCLUSION: In addition to HSCT patients, HHV-6 reactivation leading to CNS disease also occurs in settings such as following adoptive T cell therapy or biologic immunotherapy. Significant diagnostic discordance exists between testing platforms. DISCLOSURES: Rodrigo Hasbun, MD, MPH, Biofire (Consultant) Oxford University Press 2020-12-31 /pmc/articles/PMC7777935/ http://dx.doi.org/10.1093/ofid/ofaa439.361 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://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
spellingShingle Poster Abstracts
Handley, Guy H
Hasbun, Rodrigo
Okhuysen, Pablo C
51. A Review of Human Herpesvirus 6 and Central Nervous System Disease in Oncology Patients
title 51. A Review of Human Herpesvirus 6 and Central Nervous System Disease in Oncology Patients
title_full 51. A Review of Human Herpesvirus 6 and Central Nervous System Disease in Oncology Patients
title_fullStr 51. A Review of Human Herpesvirus 6 and Central Nervous System Disease in Oncology Patients
title_full_unstemmed 51. A Review of Human Herpesvirus 6 and Central Nervous System Disease in Oncology Patients
title_short 51. A Review of Human Herpesvirus 6 and Central Nervous System Disease in Oncology Patients
title_sort 51. a review of human herpesvirus 6 and central nervous system disease in oncology patients
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7777935/
http://dx.doi.org/10.1093/ofid/ofaa439.361
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