Infectious complications following chimeric antigen receptor T-cell therapy for a hematologic malignancy within 28 days
10.3760/cma.j.issn.0253-2727.2021.09.005
- VernacularTitle: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
- Author:
Yingnan LI
1
;
Mengyi DU
;
Chenggong LI
;
Yinqiang ZHANG
;
Wenjing LUO
;
Haiming KOU
;
Heng MEI
;
Yu HU
Author Information
1. 华中科技大学同济医学院附属协和医院血液科，湖北省肿瘤疾病细胞治疗临床医学研究中心，武汉 430020
- Keywords:
Chimeric antigen receptor T cell;
Hematological malignancy;
Infection clinical characteristics
- From:
Chinese Journal of Hematology
2021;42(9):739-746
- CountryChina
- Language:Chinese
-
Abstract:
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
