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:Immune-Related Adverse Events Induced by Immune Checkpoint Inhibitors and CAR-T Cell Therapy: A Comprehensive Imaging-Based Review.
Immune-Related Adverse Events Induced by Immune Checkpoint Inhibitors and CAR-T Cell Therapy: A Comprehensive Imaging-Based Review.
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免疫治疗已经彻底改变了肿瘤治疗,改善了多种癌症患者的预后。然而,由于炎症和免疫反应增强,这些治疗也与典型的免疫相关不良事件相关。这些毒性可在治疗期间任何时间出现,但在最初几个月内更为常见。任何器官和组织都可能受累,范围从轻度到危及生命。虽然有些表现较常见且通常较轻,如皮炎和结肠炎,但另一些则较罕见且更严重,如心肌炎。管理取决于严重程度,>2级毒性需暂停治疗。更严重病例使用类固醇,对于无应答的毒性可考虑免疫抑制治疗,并给予特定器官支持。多学科方法对于及时识别和管理是必需的。诊断主要为排除性诊断。它通常依赖影像学特征,并在可能时进行细胞学和/或病理学分析以确认。若临床怀疑,需进行影像学检查以评估异常的存在、范围和特征,并提示和排除鉴别诊断。这篇基于影像学的综述从多学科视角展示了与免疫检查点抑制剂和CAR-T 细胞相关的多种系统特异性毒性。临床特征、影像学表现、细胞学和组织学模式以及管理方法,并结合影像学要点,以区分这些毒性与最重要的鉴别诊断和类似病变——包括肿瘤进展、假性进展、炎症和感染——从而指导影像学和临床专家诊断免疫相关不良事件。
Immunotherapy has revolutionized oncology care, improving patient outcomes in several cancers.
However, these therapies are also associated with typical immune-related adverse events due to the enhanced inflammatory and immune response. These toxicities can arise at any time during treatment but are more frequent within the first few months. Any organ and tissue can be affected, ranging from mild to life-threatening. While some manifestations are common and more often mild, such as dermatitis and colitis, others are rarer and more severe, such as myocarditis. Management depends on the severity, with treatment being held for >grade 2 toxicities. Steroids are used in more severe cases, and immunosuppressive treatment may be considered for non-responsive toxicities, along with specific organ support. A multidisciplinary approach is mandatory for prompt identification and management. The diagnosis is primarily of exclusion.
It often relies on imaging features, and, when possible, cytologic and/or pathological analyses are performed for confirmation. In case of clinical suspicion, imaging is required to assess the presence, extent, and features of abnormalities and to evoke and rule out differential diagnoses. This imaging-based review illustrates the diverse system-specific toxicities associated with immune checkpoint inhibitors and chimeric antigen receptor T-cells with a multidisciplinary perspective.
Clinical characteristics, imaging features, cytological and histological patterns, as well as the management approach, are presented with insights into radiological tips to distinguish these toxicities from the most important differential diagnoses and mimickers-including tumor progression, pseudoprogression, inflammation, and infection-to guide imaging and clinical specialists in the pathway of diagnosing immune-related adverse events.
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