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2730. Clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy

BACKGROUND: Reactivation of cytomegalovirus (CMV) is commonly reported in lymphoma patients who undergo cellular therapy, with often poor outcomes. The risk for CMV reactivation in patients with lymphoma prior to cellular therapy is not well understood. As new alternative immunosuppressive therapies...

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Autores principales: Zubovskaia, Anna, Khawaja, Fareed, Chemaly, Roy F, Primeaux, Brian, Waleed, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679170/
http://dx.doi.org/10.1093/ofid/ofad500.2341
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author Zubovskaia, Anna
Khawaja, Fareed
Chemaly, Roy F
Primeaux, Brian
Waleed, Mohammad
author_facet Zubovskaia, Anna
Khawaja, Fareed
Chemaly, Roy F
Primeaux, Brian
Waleed, Mohammad
author_sort Zubovskaia, Anna
collection PubMed
description BACKGROUND: Reactivation of cytomegalovirus (CMV) is commonly reported in lymphoma patients who undergo cellular therapy, with often poor outcomes. The risk for CMV reactivation in patients with lymphoma prior to cellular therapy is not well understood. As new alternative immunosuppressive therapies emerge for lymphoma, understanding baseline risk for CMV reactivation is paramount to improve clinical and oncologic outcomes. Our goal was to identify risk factors, and describe outcomes associated with clinically significant CMV infection (CS-CMVi) in lymphoma patients with no prior cellular therapy. METHODS: We performed a retrospective cohort study for all lymphoma patients who underwent testing for CMV by PCR from blood between 1/2017 and 12/2020. Patients with prior history of transplantation or chimeric antigen receptor therapy were excluded. Patients with and without CS-CMVi were identified for risk factor analysis by univariate analysis. RESULTS: A total of 217 lymphoma patients were included in our analysis; CS-CMVi was identified in 41 (19%) patients. When compared to patients without CS-CMVi (control group), lymphoma patients with CS-CMVi were more likely to have history of HIV (5% vs 0%; p= 0.0350), primary central nervous system lymphoma (7% vs 1%; p= 0.0220) and relapsed disease (54% vs 25%; p= 0.0005) (Table 1). CS-CMVi was also more common if testing was done at time of relapse diagnosis (32% vs 10%; p= 0.0007), during work up for infection (98% vs 68%; p < 0.0001) and more often (3 vs 1; p < 0.0001) (table 1). Mortality and remission rates within 1 year of testing were worse in patients with CS-CMVi (table 2 and figure 1). [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: CS-CMVi in lymphoma patients is associated with poor outcomes including oncologic outcomes. Further analysis to better define patients with lymphoma at high-risk for CS-CMVi should be studied for future preventative strategies. DISCLOSURES: Fareed Khawaja, MBBS, MEDSCAPE: Honoraria|Viracor: Grant/Research Support Roy F. Chemaly, MD/MPH, Eurofins-VViracor: Grant/Research Support|Karius: Advisor/Consultant
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spelling pubmed-106791702023-11-27 2730. Clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy Zubovskaia, Anna Khawaja, Fareed Chemaly, Roy F Primeaux, Brian Waleed, Mohammad Open Forum Infect Dis Abstract BACKGROUND: Reactivation of cytomegalovirus (CMV) is commonly reported in lymphoma patients who undergo cellular therapy, with often poor outcomes. The risk for CMV reactivation in patients with lymphoma prior to cellular therapy is not well understood. As new alternative immunosuppressive therapies emerge for lymphoma, understanding baseline risk for CMV reactivation is paramount to improve clinical and oncologic outcomes. Our goal was to identify risk factors, and describe outcomes associated with clinically significant CMV infection (CS-CMVi) in lymphoma patients with no prior cellular therapy. METHODS: We performed a retrospective cohort study for all lymphoma patients who underwent testing for CMV by PCR from blood between 1/2017 and 12/2020. Patients with prior history of transplantation or chimeric antigen receptor therapy were excluded. Patients with and without CS-CMVi were identified for risk factor analysis by univariate analysis. RESULTS: A total of 217 lymphoma patients were included in our analysis; CS-CMVi was identified in 41 (19%) patients. When compared to patients without CS-CMVi (control group), lymphoma patients with CS-CMVi were more likely to have history of HIV (5% vs 0%; p= 0.0350), primary central nervous system lymphoma (7% vs 1%; p= 0.0220) and relapsed disease (54% vs 25%; p= 0.0005) (Table 1). CS-CMVi was also more common if testing was done at time of relapse diagnosis (32% vs 10%; p= 0.0007), during work up for infection (98% vs 68%; p < 0.0001) and more often (3 vs 1; p < 0.0001) (table 1). Mortality and remission rates within 1 year of testing were worse in patients with CS-CMVi (table 2 and figure 1). [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: CS-CMVi in lymphoma patients is associated with poor outcomes including oncologic outcomes. Further analysis to better define patients with lymphoma at high-risk for CS-CMVi should be studied for future preventative strategies. DISCLOSURES: Fareed Khawaja, MBBS, MEDSCAPE: Honoraria|Viracor: Grant/Research Support Roy F. Chemaly, MD/MPH, Eurofins-VViracor: Grant/Research Support|Karius: Advisor/Consultant Oxford University Press 2023-11-27 /pmc/articles/PMC10679170/ http://dx.doi.org/10.1093/ofid/ofad500.2341 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Zubovskaia, Anna
Khawaja, Fareed
Chemaly, Roy F
Primeaux, Brian
Waleed, Mohammad
2730. Clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy
title 2730. Clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy
title_full 2730. Clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy
title_fullStr 2730. Clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy
title_full_unstemmed 2730. Clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy
title_short 2730. Clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy
title_sort 2730. clinically significant cytomegalovirus infection in patients with lymphoma and no prior cellular therapy
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10679170/
http://dx.doi.org/10.1093/ofid/ofad500.2341
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