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B 细胞淋巴瘤患者 CD19 靶向 CAR-T 治疗后 SARS-CoV-2 奥密克戎变异株感染的结局与危险因素

英文原题:Outcomes and risk factors of SARS-CoV-2 omicron variant in B-cell lymphoma patients following CD19 targeted CAR-T therapy.

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Outcomes and risk factors of SARS-CoV-2 omicron variant in B-cell lymphoma patients following CD19 targeted CAR-T therapy.

PubMed 2023/11/14(内容时间) Cancer Med Q2 · IF 3.5(JCR 2025)

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研究概要

通过本研究,我们得出结论:B 细胞淋巴瘤患者在接受 CD19 靶向 CAR-T 治疗后面对奥密克戎感染时,其结局有所改善,但积极的预防措施对具有高危因素的患者尤为关键。

中文摘要

此前对于接受CD19靶向CAR-T 细胞治疗的B细胞淋巴瘤患者感染SARS-CoV-2奥密克戎变异株后的感染率和病死率所知甚少,重症危险因素更缺乏资料。

奥密克戎流行期间,我们在中国5家细胞免疫治疗中心开展多中心回顾性研究,分析曾接受CD19靶向CAR-T 治疗的复发/难治性(R/R)B细胞淋巴瘤患者的详细资料。

共纳入154例患者。

数据收集时,52例(33.8%)未感染;74例(48.1%)为门诊轻症,其中包括9例无症状感染;22例(14.3%)为中度疾病;6例(3.9%)为重症。3例重症患者死于COVID-19;全部入组患者的死亡率为1.9%,感染者中的死亡率为2.9%。年龄超过60岁或患糖尿病(DM)的患者更易发生重症(分别为p=0.0057和p=0.0497)。CAR-T 输注距今不足6个月的患者也更易发生重症(p=0.0011)。多变量Logistic回归显示,6个月内接受CAR-T 输注与重症风险显著升高相关(相对风险[RR] 40.92;置信区间[CI] 4.03–415.89;p=0.002)。

本研究显示,接受CD19靶向CAR-T 治疗的B细胞淋巴瘤患者感染奥密克戎后的结局有所改善,但对存在高危因素的患者尤其需要采取积极预防措施。

展开英文摘要原文

Little was known on infection and mortality rates, still less the risk factors of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) omicron variant in B-cell lymphoma patients following CD19 targeted chimeric antigen receptor T cell (CAR-T). AIMS: We performed a retrospective multicenter study and analyzed the details of relapsed/refractory (R/R) B-cell lymphoma patients who received CD19 targeted CAR-T heretofore in five cellular immunotherapy centers in China during the omicron wave. MATERIALS &

One hundred fifty-four patients were enrolled in this study.

Among them, 52 patients (33.8%) were uninfected, 74 patients (48.1) had ambulatory mild disease (including nine patients of asymptomatic infection), 22 patients (14.3%) had moderate disease and six patients (3.9%) had severe disease when data collected up. Three patients with severe disease died from COVID-19, the death rate was 1.9% for all enrolled patients, and 2.9% for infected patients. We also found that patients over 60 years old or with diabetes mellitus (DM) tend to develop severe disease (p = 0.0057 and p = 0.0497, respectively). Patients had CAR-T infusion within 6 months also tend to have severe disease (p = 0.0011). In multivariate logistic regression model, CAR-T infusion within 6 months (relative risk (RR) 40.92; confidence interval (CI) 4.03-415.89; p = 0.002) were associated with significantly higher risk of severe disease.

Through this study, we conclude that the outcome for B-cell lymphoma patients following CD19 targeted CAR-T therapy when facing omicron infection was improved, but aggressive precautionary measures were particularly crucial for patients with high risk factors.

论文信息

作者
Xiao X、Chen P、Zhong Y、Luo X、Liu Y、Lu Y、Jin X、Qian W
单位
Department of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.China
文献类型
多中心研究 · 非美国政府资助研究
期刊
Cancer medicine2023 Nov
原文标识
PubMed 37962082 · DOI 10.1002/cam4.6657