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:CAR-T cell: Toxicities issues: Mechanisms and clinical management.
CAR-T cell: Toxicities issues: Mechanisms and clinical management.
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CAR-T 细胞是经过修饰的 T 细胞,表达靶向特定抗原的嵌合抗原受体。它们已经彻底改变了 B 细胞恶性肿瘤(侵袭性淋巴瘤、B-ALL)的治疗,这也为应用于许多其他疾病(骨髓瘤、AML、实体瘤等)带来了希望。然而,这些疗法与新型且特异性的毒性相关(细胞因子释放综合征和神经毒性)。这些并发症虽然大多在常规住院病房中管理,但有时可能危及生命,导致患者入住重症监护病房。管理主要依赖抗 IL6R(tocilizumab)和糖皮质激素。然而,最佳治疗方案仍存在争议,最严重形式的管理更缺乏规范。除 CRS 和 ICANS 外,感染、血细胞减少和低丙种球蛋白血症也是其他常见并发症。本文综述了这些毒性的机制、危险因素、临床表现和管理。
CAR-T cells are modified T cells expressing a chimeric antigen receptor targeting a specific antigen. They have revolutionized the treatment of B cell malignancies (aggressive lymphomas, B-ALL), and this has raised hopes for application in many other pathologies (myeloma, AML, solid tumors, etc.) .
However, these therapies are associated with novel and specific toxicities (cytokine release syndrome and neurotoxicity). These complications, although mostly managed in a conventional hospitalization unit, can sometimes be life threatening, leading to admission of patients to the intensive care unit. Management relies mainly on anti-IL6R (tocilizumab) and corticosteroids.
However, the optimal treatment regimen is still a matter of debate, and the management of the most severe forms is even less well codified.
In addition to CRS and ICANS, infections, cytopenia and hypogammaglobulinemia are other frequent complications. This article reviews the mechanisms, risk factors, clinical presentation, and management of these toxicities.
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