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:Cytokine release syndrome after CAR T-cell therapy for B-cell acute lymphoblastic leukemia in children and young adolescents: storms make trees take deeper roots.
Cytokine release syndrome after CAR T-cell therapy for B-cell acute lymphoblastic leukemia in children and young adolescents: storms make trees take deeper roots.
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随着 CAR-T 细胞疗法在儿童 B-ALL 中越来越可及和广泛应用,CRS 的最佳管理变得日益重要。早期识别和及时管理已有所改善。进一步的信息将有助于我们确定 tocilizumab 和皮质类固醇的最佳使用时机。持续的基础研究结合临床研究和生物标志物的发现,将为了解 CRS 病理生理学以及患者和/或细胞靶向治疗提供有价值的见解。
嵌合抗原受体(CAR)T细胞已经彻底改变了癌症治疗,显示出显著的成功,包括治疗儿童B细胞急性淋巴细胞白血病(B-ALL)。尽管其疗效显著,细胞因子释放综合征(CRS)仍是常见的早期不良事件,在严重情况下可能危及生命,其源于免疫系统针对肿瘤的靶向激活。涵盖领域:本综述聚焦于接受CAR-T 细胞治疗B-ALL的儿童和年轻成人中的CRS。探讨CRS的病理生理学、临床表现和发生率,强调共识定义和分级的重要性,以便根据症状严重程度统一治疗。我们将讨论CRS的标准治疗以及新方法。我们将强调在不影响免疫细胞抗肿瘤激活疗效的前提下管理CRS的重要性。
INTRODUCTION: Chimeric antigen receptor (CAR) T-cells have revolutionized cancer treatment, showing significant success, including treatment of pediatric B-cell acute lymphoblastic leukemia (B-ALL). Despite their efficacy, cytokine release syndrome (CRS) emerges as a common early adverse effect that can be life threatening in severe cases, resulting from the immune system's targeted activation against tumors.
AREAS COVERED: This review concentrates on CRS in children and young adults undergoing CAR T-cell therapy for B-ALL. It explores CRS pathophysiology, clinical presentation, and incidence, emphasizing the importance of a consensus definition and grading to homogenize the treatment according to the severity of symptoms.
We will discuss the standard of care treatment of CRS but also novel approaches.
We will highlight the importance of managing CRS without compromising the efficacy of immune cell activation against tumors. EXPERT OPINION: As CAR T-cell therapy in pediatric B-ALL become increasingly available and used, optimal management of CRS becomes increasingly important. Early recognition and timely management has improved.
Further information will aid us to identify optimal timing of tocilizumab and corticosteroids. Continued bench research coupled with clinical studies and biomarker discovery will allow for valuable insights into CRS pathophysiology and patient and/or cell-targeted treatments.
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