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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Cardiotoxicity of Chimeric Antigen Receptor T-Cell (CAR-T) Therapy: Pathophysiology, Clinical Implications, and Echocardiographic Assessment.
Cardiotoxicity of Chimeric Antigen Receptor T-Cell (CAR-T) Therapy: Pathophysiology, Clinical Implications, and Echocardiographic Assessment.
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当代抗癌免疫治疗中的CAR-T 细胞疗法已显著改变了多种既往预后较差的血液系统恶性肿瘤的治疗格局。临床改善和生存获益揭示了心脏毒性的风险,其范围从轻微影响到严重心脏不良事件,甚至包括死亡。即使患者已存在心血管危险因素,也应考虑免疫治疗,从而增加了心脏毒性的潜在危害。CAR-T 治疗常导致细胞因子释放综合征(CRS),而循环细胞因子维持炎症激活,形成正反馈机制。及时诊断和治疗CAR-T 心脏毒性可能显著改善预后并减轻心血管并发症相关负担。临床和超声心动图检查对于在CAR-T 治疗期间进行个体化评估和随访至关重要。本综述旨在总结CAR-T 相关心脏毒性的病理生理学、临床意义和超声心动图评估,以启迪未来研究的新方向。
Contemporary anticancer immunotherapy with chimeric antigen receptor T-cell (CAR-T) therapy has dramatically changed the treatment of many hematologic malignancies previously associated with poor prognosis. The clinical improvement and the survival benefit unveiled the risk of cardiotoxicity, ranging from minimal effects to severe cardiac adverse events, including death. Immunotherapy should also be proposed even in patients with pre-existing cardiovascular risk factors, thereby increasing the potential harm of cardiotoxicity.
CAR-T therapy frequently results in cytokine release syndrome (CRS), and inflammatory activation is sustained by circulating cytokines that foster a positive feedback mechanism. Prompt diagnosis and treatment of CAR-T cardiotoxicity might significantly improve outcomes and reduce the burden associated with cardiovascular complications.
Clinical and echocardiographic examinations are crucial to perform a tailored evaluation and follow-up during CAR-T treatment. This review aims to summarize the pathophysiology, clinical implications, and echocardiographic assessment of CAR-T-related cardiotoxicity to enlighten new avenues for future research.
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