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血液肿瘤患者回输嵌合抗原受体T细胞后28天内感染病原学和临床特征分析

OBJECTIVE: To explore the incidence, clinical and microbiological characteristics and risk factors of infection in patients with acute lymphoblastic (ALL), non-Hodgkin lymphoma (NHL), and multiple myeloma (MM) within 28 days after CAR-T cell infusion. It provides data support for early identificatio...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607031/
https://www.ncbi.nlm.nih.gov/pubmed/34753228
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.09.005
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collection PubMed
description OBJECTIVE: To explore the incidence, clinical and microbiological characteristics and risk factors of infection in patients with acute lymphoblastic (ALL), non-Hodgkin lymphoma (NHL), and multiple myeloma (MM) within 28 days after CAR-T cell infusion. It provides data support for early identification of infection and the rational use of antibacterial drugs in these patients. METHODS: We retrospectively analyzed the baseline data of 170 patients with ALL, NHL and MM who received chimeric antigen receptor-modified T (CAR-T)-cell treatment in the Department of Hematology of Wuhan Union Hospital from January 2016 to December 2020, and the clinical characteristics of infection within 28 days after infusion, including 72 patients with ALL, 56 patients with NHL, and 42 patients with MM; we used Poisson regression and Cox proportional hazard regression models to assess high-risk factors for infection before and after infusion, respectively. RESULTS: Among 170 patients, 119 infections occurred in 99 patients within 28 days, with a cumulative infection rate of 58.2%. Seventy-eight patients had 98 bacterial infections and the cumulative incidence of bacterial infection was 45.9%. The infection density was 2.01, and the median time for the first infection was about 12 days after infusion. The adjusted baseline characteristic model showed that ALL patients, previous 30 days of infection history, refractory disease, absolute neutrophil count (ANC)<0.5×10(9)/L before infusion and ≥4 prior antitumor treatment regimens had a higher infection density within 28 days; grade 3 or 4 CRS was the only high-risk factor related to infection after infusion in the multivariate analysis. CONCLUSION: Infection is a common complication of CAR-T cell therapy in patients with hematologic malignancy. Bacterial infections occur in most patients regardless of the type of disease. ALL patients, previous 30 days of infection history, refractory disease, ANC<0.5 × 10(9)/L before infusion and grade 3 or 4 CRS are risk factors for infection. Chinese Clinical Trial Register: ChiCTR-OIC-17011180, ChiCTR1800018143
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spelling pubmed-86070312021-12-07 血液肿瘤患者回输嵌合抗原受体T细胞后28天内感染病原学和临床特征分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To explore the incidence, clinical and microbiological characteristics and risk factors of infection in patients with acute lymphoblastic (ALL), non-Hodgkin lymphoma (NHL), and multiple myeloma (MM) within 28 days after CAR-T cell infusion. It provides data support for early identification of infection and the rational use of antibacterial drugs in these patients. METHODS: We retrospectively analyzed the baseline data of 170 patients with ALL, NHL and MM who received chimeric antigen receptor-modified T (CAR-T)-cell treatment in the Department of Hematology of Wuhan Union Hospital from January 2016 to December 2020, and the clinical characteristics of infection within 28 days after infusion, including 72 patients with ALL, 56 patients with NHL, and 42 patients with MM; we used Poisson regression and Cox proportional hazard regression models to assess high-risk factors for infection before and after infusion, respectively. RESULTS: Among 170 patients, 119 infections occurred in 99 patients within 28 days, with a cumulative infection rate of 58.2%. Seventy-eight patients had 98 bacterial infections and the cumulative incidence of bacterial infection was 45.9%. The infection density was 2.01, and the median time for the first infection was about 12 days after infusion. The adjusted baseline characteristic model showed that ALL patients, previous 30 days of infection history, refractory disease, absolute neutrophil count (ANC)<0.5×10(9)/L before infusion and ≥4 prior antitumor treatment regimens had a higher infection density within 28 days; grade 3 or 4 CRS was the only high-risk factor related to infection after infusion in the multivariate analysis. CONCLUSION: Infection is a common complication of CAR-T cell therapy in patients with hematologic malignancy. Bacterial infections occur in most patients regardless of the type of disease. ALL patients, previous 30 days of infection history, refractory disease, ANC<0.5 × 10(9)/L before infusion and grade 3 or 4 CRS are risk factors for infection. Chinese Clinical Trial Register: ChiCTR-OIC-17011180, ChiCTR1800018143 Editorial office of Chinese Journal of Hematology 2021-09 /pmc/articles/PMC8607031/ /pubmed/34753228 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.09.005 Text en 2021年版权归中华医学会所有 https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 License.
spellingShingle 论著
血液肿瘤患者回输嵌合抗原受体T细胞后28天内感染病原学和临床特征分析
title 血液肿瘤患者回输嵌合抗原受体T细胞后28天内感染病原学和临床特征分析
title_full 血液肿瘤患者回输嵌合抗原受体T细胞后28天内感染病原学和临床特征分析
title_fullStr 血液肿瘤患者回输嵌合抗原受体T细胞后28天内感染病原学和临床特征分析
title_full_unstemmed 血液肿瘤患者回输嵌合抗原受体T细胞后28天内感染病原学和临床特征分析
title_short 血液肿瘤患者回输嵌合抗原受体T细胞后28天内感染病原学和临床特征分析
title_sort 血液肿瘤患者回输嵌合抗原受体t细胞后28天内感染病原学和临床特征分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607031/
https://www.ncbi.nlm.nih.gov/pubmed/34753228
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.09.005
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