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既存自身免疫与肿瘤治疗中 CAR-T 细胞疗法毒性的关联

英文原题:Associations Between Pre-Existing Autoimmunity and Chimeric Antigen Receptor T Cell Therapy Toxicity for Cancer Treatment.

查看英文原题

Associations Between Pre-Existing Autoimmunity and Chimeric Antigen Receptor T Cell Therapy Toxicity for Cancer Treatment.

PubMed 2025/10/01(内容时间) ACR Open Rheumatol Q2 · IF 2.9(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

嵌合抗原受体(CAR)T细胞疗法正在用于治疗自身免疫性疾病的研究中,但该人群中的安全性数据有限。本研究旨在评估既往自身免疫性疾病是否会增加因血液系统恶性肿瘤接受CAR-T 治疗患者的重大毒性或住院时间。

本回顾性队列研究利用美国国家住院样本数据库(2021–2022年),调查接受CAR-T 治疗的成年患者住院期间结局,并比较有无既往自身免疫性疾病的患者。多变量回归模型校正年龄、性别、种族、癌症类型及合并症后,评估其与住院时间、重大毒性和住院死亡的关联。

1321例接受CAR-T 治疗的患者中,62例(4.7%)确诊有自身免疫性疾病。与无既往自身免疫性疾病者相比,这些患者住院时间显著较短,平均减少2.1天(95%置信区间0.5–3.6)。既往自身免疫患者发生重大毒性的比例也较低(67.7%比78.6%;校正后比值比0.55;95%置信区间0.31–0.99)。两组住院死亡率无显著差异。

因癌症接受CAR-T 治疗后,既往自身免疫性疾病患者住院时间较短、重大毒性风险较低。这为该人群接受CAR-T 治疗的安全性提供了一定依据,也补充了CAR-T 用于治疗自身免疫性疾病的研究数据。

展开英文摘要原文

Chimeric antigen receptor (CAR) T cell therapy is being investigated to treat individuals with autoimmune diseases. Data regarding the safety of CAR T cell therapy in this population are limited. We aimed to assess whether pre-existing autoimmune disease was associated with an increase in major toxicity or hospital length of stay (LOS) among patients receiving CAR T cell therapy for the treatment of hematologic cancer.

This retrospective cohort study used data from the National Inpatient Sample (2021-2022) to investigate in-hospital outcomes in adult patients receiving CAR T cell therapy. Comparisons were drawn between patients with and without pre-existing autoimmune disease. Multivariable regression models with adjustment for age, sex, race, cancer type, and comorbidities assessed associations with hospital LOS, major toxicity, and inpatient mortality.

Among 1,321 patients receiving CAR T cell therapy, 62 (4.7%) had diagnosed autoimmune disease. Patients with pre-existing autoimmunity had a significantly shorter hospital stay compared with patients without, with a mean reduction of 2.1 days (95% confidence interval [CI] 0.5-3.6). Major toxicity was less frequent in patients with pre-existing autoimmunity than patients without (67.7% vs 78.6%, respectively; adjusted odds ratio 0.55; 95% CI 0.31-0.99). Inpatient mortality did not differ significantly between groups.

Patients with pre-existing autoimmune disease had shorter hospital stays and lower risk of major toxicity following CAR T cell therapy for cancer treatment, offering reassurance as to its safety in this population while providing additional data for research studies of CAR T cell therapy to treat autoimmune diseases.

论文信息

作者
Challener GJ、Wang C、Gritsch D、Usiskin IM、Walton ZE、Kohler MJ、Choi H、Sparks JA
第一作者单位
Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.United States
通讯作者单位
Harvard Medical School and Brigham and Women's Hospital, Boston, Massachusetts.United States
期刊
ACR open rheumatology2025 Oct
原文标识
PubMed 41110994 · DOI 10.1002/acr2.70112