CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The clinical picture of ICANS after CAR-T cell therapy in critically ill patients: A retrospective clustering analysis of a multicentre multinational cohort study.
The clinical picture of ICANS after CAR-T cell therapy in critically ill patients: A retrospective clustering analysis of a multicentre multinational cohort study.
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CAR-T 细胞治疗存在显著风险,包括 ICANS。关于入住 ICU 患者中 ICANS 表现和结局的数据有限,且预测哪些患者会发生重度 ICANS 仍然具有挑战性。这是一项国际性、多中心、观察性队列研究的预先计划亚组研究,该队列研究纳入 241 例因血液系统恶性肿瘤接受 CAR-T 细胞治疗并入住 ICU 的患者,重点关注发生 ICANS 的患者。
我们旨在详细描述症状,并使用层次聚类分析来识别神经系统症状表现的独特模式。100 例患者(41.5%)检出 ICANS,中位年龄 61 岁。大多数患者(93%)患有非霍奇金淋巴瘤。38% 的患者发生重度 ICANS,与更长的症状持续时间相关(p = 0.02)。在整个队列中,神经系统症状的中位持续时间为 5(IQR 1-8)天,对于孤立性 ICANS 患者也更长(中位 16 天(IQR 11-24,p = 0.001))。层次聚类揭示了四个症状重叠极少的独特聚类:聚类 1:轻度或无临床症状,主要为意识模糊(11.2%);聚类 2:意识模糊(78.9%)和嗜睡(47.4%)发生率高,伴癫痫发作(42.1%)和昏迷(21.1%)的显著风险;聚类 3:以震颤(75%)和注意力缺陷(37.5%)为主;聚类 4:失语(70.3%)、书写困难(37.8%)和定向障碍(27%)发生率高。神经系统症状的聚类具有统计学显著性(p < 0.001)。
本研究对 ICANS 进行了详细刻画,突出了神经系统症状的独特模式。这些发现可为临床医生提供信息,特别是关于 ICU 入住的风险和时机。
CAR T-cell therapy carries significant risks, including ICANS. There is limited data on ICANS presentation and outcomes in patients admitted to ICU and it is still challenging to predict those who will have severe ICANS. This is a pre-planned substudy of an international, multicenter, observational cohort study of 241 CAR T-cell recipients for hematological malignancies, admitted to the ICU, focusing on those who developed ICANS.
We aimed for a detailed description of symptoms and hierarchical clustering analysis was used to identify distinct patterns of neurological symptom presentation. ICANS was identified in 100 patients (41. 5%), median age of 61 years. Most patients (93%) had non-Hodgkin lymphoma. Severe ICANS occurred in 38% of patients, associated with longer duration of symptoms ( p = 0. 02). On the whole cohort, the median duration of neurological symptoms was 5 (IQR 1-8) days and was also longer for patients with isolated ICANS (median of 16 days (IQR 11-24, p = 0.
001)). Hierarchical clustering revealed four distinct clusters with minimal symptom overlap: Cluster 1: Mild or no symptoms, primarily confusion (11. 2%); Cluster 2: High incidence of confusion (78. 9%) and drowsiness (47. 4%), with significant risks of seizures (42. 1%) and coma (21. 1%); Cluster 3: Predominantly tremor (75%) and attention deficit (37. 5%); Cluster 4: High incidence of aphasia (70. 3%), dysgraphia (37. 8%), and disorientation (27%). The clustering of neurological symptoms was statistically significant ( p < 0. 001).
This study provides a detailed characterization of ICANS, highlighting distinct patterns of neurological symptoms.
These findings could inform clinicians, particularly regarding the risk and timing of ICU admission.
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