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2708. Infectious Complications Among CD19 Chimeric Antigen Receptor T-cell Recipients
BACKGROUND: Current data on infectious complications of chimeric antigen receptor (CAR) T-cell therapy are limited to single center retrospective cohort studies. Presented here is a subset of patients from a multicenter retrospective cohort study including recipients of CAR T-cell therapy at Duke Un...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677729/ http://dx.doi.org/10.1093/ofid/ofad500.2319 |
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author | Huggins, Jonathan Messina, Julia A Saullo, Jennifer Andermann, Tessa Smith, Melody Schrum, Daniel Eberwein, Erin Kennedy, Erin Rowe-Nichols, Krista Kelsey, Christopher Choi, Taewoong McKinney, Matthew Galal, Ahmed Kang, Yubin |
author_facet | Huggins, Jonathan Messina, Julia A Saullo, Jennifer Andermann, Tessa Smith, Melody Schrum, Daniel Eberwein, Erin Kennedy, Erin Rowe-Nichols, Krista Kelsey, Christopher Choi, Taewoong McKinney, Matthew Galal, Ahmed Kang, Yubin |
author_sort | Huggins, Jonathan |
collection | PubMed |
description | BACKGROUND: Current data on infectious complications of chimeric antigen receptor (CAR) T-cell therapy are limited to single center retrospective cohort studies. Presented here is a subset of patients from a multicenter retrospective cohort study including recipients of CAR T-cell therapy at Duke University, University of North Carolina at Chapel Hill, and Stanford University. METHODS: In a retrospective cohort of 66 patients who received CD19 CAR T-cell therapy Duke University between January 1, 2018 and August 31, 2021 rates and characteristics of bacterial, viral, and fungal infections within the first year after CAR T-cell infusion are described. Demographic, baseline clinical, and outcome variables are compared between patients who developed infection and those who did not. RESULTS: Forty-nine total infections occurred in 29 (43.9%) patients within 1 year of CAR T-cell infusion. Patients who developed infection were more likely to have an underlying malignancy other than diffuse large B-cell lymphoma (34% vs 8%, p = 0.031), and to have developed immune effector cell-associated neurotoxicity syndrome (62% vs. 32%, p = 0.016). Viral (23/49, 46.9%) and bacterial (20/49, 40.8%) pathogens predominated and infections most often involved the bloodstream (19/49, 38.8%) and lung (18/49, 36.7%).There were no statistically significant differences between rates of bacterial and viral infection based on time since CAR T-cell infusion (≤30 days vs 30 – 90 days vs >90 days), though fungal infections only occurred after 90 days in patients with relapse of their underlying disease. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Infectious complications after CAR T-cell therapy are common within the first year of infusion. Bacterial and viral infections predominate while fungal infections are rare and occurred only in patients with relapsed disease. DISCLOSURES: Melody Smith, MD, MS, BMS: Advisor/Consultant Krista Rowe-Nichols, RN, MSN, AOCNS, Bristol Myers Squibb: Advisor/Consultant|Kite Pharmaceuticals: Advisor/Consultant|Kite Pharmaceuticals: Speaker Bureau Christopher Kelsey, MD, Colgate-Palmolive: Expert Testimony|Johnson and Johnson: Expert Testimony Taewoong Choi, MD, Janssen biotech: Honoraria Matthew McKinney, MD, ADC Therapeutics: Advisor/Consultant|ADC Therapeutics: Honoraria|Beigene: Grant/Research Support|Beigene: Honoraria|Epizyme: Advisor/Consultant|Genentech: Advisor/Consultant|Genentech: Grant/Research Support|Genentech: Honoraria|Gilead/Kite: Advisor/Consultant|Gilead/Kite: Honoraria|Incyte: Grant/Research Support|Novartis: Advisor/Consultant|Seagen, Inc.: Advisor/Consultant|Takeda: Advisor/Consultant|TG therapeutics: Advisor/Consultant |
format | Online Article Text |
id | pubmed-10677729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106777292023-11-27 2708. Infectious Complications Among CD19 Chimeric Antigen Receptor T-cell Recipients Huggins, Jonathan Messina, Julia A Saullo, Jennifer Andermann, Tessa Smith, Melody Schrum, Daniel Eberwein, Erin Kennedy, Erin Rowe-Nichols, Krista Kelsey, Christopher Choi, Taewoong McKinney, Matthew Galal, Ahmed Kang, Yubin Open Forum Infect Dis Abstract BACKGROUND: Current data on infectious complications of chimeric antigen receptor (CAR) T-cell therapy are limited to single center retrospective cohort studies. Presented here is a subset of patients from a multicenter retrospective cohort study including recipients of CAR T-cell therapy at Duke University, University of North Carolina at Chapel Hill, and Stanford University. METHODS: In a retrospective cohort of 66 patients who received CD19 CAR T-cell therapy Duke University between January 1, 2018 and August 31, 2021 rates and characteristics of bacterial, viral, and fungal infections within the first year after CAR T-cell infusion are described. Demographic, baseline clinical, and outcome variables are compared between patients who developed infection and those who did not. RESULTS: Forty-nine total infections occurred in 29 (43.9%) patients within 1 year of CAR T-cell infusion. Patients who developed infection were more likely to have an underlying malignancy other than diffuse large B-cell lymphoma (34% vs 8%, p = 0.031), and to have developed immune effector cell-associated neurotoxicity syndrome (62% vs. 32%, p = 0.016). Viral (23/49, 46.9%) and bacterial (20/49, 40.8%) pathogens predominated and infections most often involved the bloodstream (19/49, 38.8%) and lung (18/49, 36.7%).There were no statistically significant differences between rates of bacterial and viral infection based on time since CAR T-cell infusion (≤30 days vs 30 – 90 days vs >90 days), though fungal infections only occurred after 90 days in patients with relapse of their underlying disease. [Figure: see text] [Figure: see text] [Figure: see text] CONCLUSION: Infectious complications after CAR T-cell therapy are common within the first year of infusion. Bacterial and viral infections predominate while fungal infections are rare and occurred only in patients with relapsed disease. DISCLOSURES: Melody Smith, MD, MS, BMS: Advisor/Consultant Krista Rowe-Nichols, RN, MSN, AOCNS, Bristol Myers Squibb: Advisor/Consultant|Kite Pharmaceuticals: Advisor/Consultant|Kite Pharmaceuticals: Speaker Bureau Christopher Kelsey, MD, Colgate-Palmolive: Expert Testimony|Johnson and Johnson: Expert Testimony Taewoong Choi, MD, Janssen biotech: Honoraria Matthew McKinney, MD, ADC Therapeutics: Advisor/Consultant|ADC Therapeutics: Honoraria|Beigene: Grant/Research Support|Beigene: Honoraria|Epizyme: Advisor/Consultant|Genentech: Advisor/Consultant|Genentech: Grant/Research Support|Genentech: Honoraria|Gilead/Kite: Advisor/Consultant|Gilead/Kite: Honoraria|Incyte: Grant/Research Support|Novartis: Advisor/Consultant|Seagen, Inc.: Advisor/Consultant|Takeda: Advisor/Consultant|TG therapeutics: Advisor/Consultant Oxford University Press 2023-11-27 /pmc/articles/PMC10677729/ http://dx.doi.org/10.1093/ofid/ofad500.2319 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 Huggins, Jonathan Messina, Julia A Saullo, Jennifer Andermann, Tessa Smith, Melody Schrum, Daniel Eberwein, Erin Kennedy, Erin Rowe-Nichols, Krista Kelsey, Christopher Choi, Taewoong McKinney, Matthew Galal, Ahmed Kang, Yubin 2708. Infectious Complications Among CD19 Chimeric Antigen Receptor T-cell Recipients |
title | 2708. Infectious Complications Among CD19 Chimeric Antigen Receptor T-cell Recipients |
title_full | 2708. Infectious Complications Among CD19 Chimeric Antigen Receptor T-cell Recipients |
title_fullStr | 2708. Infectious Complications Among CD19 Chimeric Antigen Receptor T-cell Recipients |
title_full_unstemmed | 2708. Infectious Complications Among CD19 Chimeric Antigen Receptor T-cell Recipients |
title_short | 2708. Infectious Complications Among CD19 Chimeric Antigen Receptor T-cell Recipients |
title_sort | 2708. infectious complications among cd19 chimeric antigen receptor t-cell recipients |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677729/ http://dx.doi.org/10.1093/ofid/ofad500.2319 |
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